Azepines . Part 1 [[electronic resource] /] / Jeffrey W.H. Watthey, James Stanton, Norton P. Peet; editor, Andre Rosowsky |
Pubbl/distr/stampa | New York, : John Wiley and Sons, 1984 |
Descrizione fisica | 1 online resource (841 p.) |
Disciplina |
547.593
547/.59/05 547/.593 |
Altri autori (Persone) |
RosowskyAndre
RenfroeBurt WattheyJeffrey W. H |
Collana | Chemistry of heterocyclic compounds |
Soggetto topico |
Azepines
Chemistry |
Soggetto genere / forma | Electronic books. |
ISBN |
1-282-30195-0
9786612301957 0-470-18721-2 0-470-18873-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
AZEPINES; Contents; CHAPTER I. DIBENZAZEPINES AND OTHER TRICYCLIC AZEPINES; I. Introduction; II. 3,6,7-Systems; 1. Oxireno[d][2]benzazepines; 2. Benzo[b]cycloprop[d]azepines; 3. Benzo[d]cycloprop[b]azepines; III. 5,5,7-Systems; 1. Cyclopenta[c]tetrazolo[1,5-a]azepines; 2. 2,2a,3-Trithia(2a-Siv)-4a-azacyclopent[cd]azulenes; 3. Dipyrazolo[4,3-c:3',4'-e]azepines; 4. Thiazolo[2',3':2,3]imidazo[1,5-a]azepines; 5. Dipyrrolo[1,2-a:2',3'-d]azepines; 6. Azepino[2,1,7-cd]pyrrolizines; 7. Furo[3,2-c]pyrrolo[1,2-a]azepines; 8. Dithieno[2,3-e.'3',2'-e]azepines; IV. 5,6,7-Systems
1. Tetrazolo[5,1-a][2]benzazepines2. Tetrazolo[5,1-b][3]benzazepines; 3. 1,2,4-Triazolo[3,4-b][3]benzazepines; 4. Azepino[2,1-b]benzoxazoles; 5. Oxazolo[2,3-a][2]benzazepines; 6. Isothiazolo[5',4':4,5]pyrimido[1,2-a]azepines; 7. Azepino[2,l-b]benzothiazoles; 8. Isothiazolo[3,2,-b][3]benzazepines; 9. Thiazolo[2,3-a][2]benzazepines; 10. Thiazolo[2,3-b][3]benzazepines; 11. Thiazolo[3,2-b][2]benzazepines; 12. Thiazolo[3,2-a][1]benzazepines; 13. Azepino[2,1-b]benzoselenazoles; 14. Azepino[1,2-e]purines; 15. Azepino[2,1-f]purines; 16. Pyrazolo[3',4':4,5]pyrimido[1,2-a]azepines 17. 2a,4,9a-Triazabenz[c,d]azulenes18. Pyrido[3',2':4,5]imidazo[1,2-a]azepines; 19. Pyrido[3',4':4,5]irnidazo[1,2-a]azepines; 20. Azepino[1,2-a]benzimidazoles; 21. Imidazo[2,1-a][2]benzazepines; 22. Imidazo[2,1-b][3]benzazepines; 23. Imidazo[4,5-jk]benzazepines; 24. Pyrazolo[3,4-b]benzazepines; 25. Pyrazolo[3,4-c][1]benzazepines; 26. Pyrazolo[3,4-c][2]benzazepines; 27. Pyrazolo[4,3-d][2]benzazepines; 28. 1,3-Dioxolo[4,5-h][2]benzazepines; 29. 1,3-Dioxolo[4,5-h][3]benzazepines; 30. [1,3]Oxazino[3,2-a]pyrrolo[2,3-f]azepines; 31. Azepino[2,1,7-cd]indolizines 32. Pyrido[3',2':4,5]pyrrolo[2,3-c]azepines33. Pyrido[3',4':4,5]pyrrolo[2,3-c]azepines; 34. Azepino[1,2-a]indoles; 35. Azepino[2,1-i]indoles; 36. Azepino[2,3-b]indoles; 37. Azepino[3,2-b]indoles; 38. Azepino[3,4-b]indoles; 39. Azepino[3,2,l-hi]indoles; 40. Azepino[3,4,5-cd]indoles; 41. Azepino[4,3-b]indoles; 42. Azepino[4,3,2-cd]dindoles; 43. Azepino[4,5-b]indoles; 44. Azepino[5,4,3-cd]indoles; 45. Azepino[4,5-e]indoles; 46. Azepino[4,5-f]indoles; 47. Azepino[4,5-g]indoles; 48. Azepino[2,1-a]isoindoles; 49. Pyrrolo[l,2-a][1]benzazepines; 50. Pyrrolo[l,2-b][2]benzazepines 51. Pyrrolo[2,1-b][3]benzazepines52. Furo[2',3':4,5]pyrimido[1,2-a]azepines; 53. Benzofuro[2,3-b]azepines; 54. Benzofuro[2,3-c]azepines; 55. Benzofuro[3,2-b]azepines; 56. Benzofuro[3,2-c]azepines; 57. Furo[2,3-g]benzazepines; 58. Furo[3,2-g][1]benzazepines; 59. Furo[3,2-g][2]benzazepines; 60. Furo[3,2-i][1]benzazepines; 61. Furo[3,2-i][2]benzazepines; 62. Furo[3,4-c][1]benzazepines; 63. Thieno[2',3':4,5]pyrimido[1,2-a]azepines; 64. Thieno[4,3,2-ef][1]benzazepines; 65. [1]Benzothieno[2,3-c]azepines; 66. [1]Benzothieno[3,2-b]azepines; 67. [1]Benzothieno[3,2-c]azepines 68. Thieno[2,3-c][1]benzazepines |
Record Nr. | UNINA-9910144276103321 |
New York, : John Wiley and Sons, 1984 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Azepines . Part 1 [[electronic resource] /] / Jeffrey W.H. Watthey, James Stanton, Norton P. Peet; editor, Andre Rosowsky |
Pubbl/distr/stampa | New York, : John Wiley and Sons, 1984 |
Descrizione fisica | 1 online resource (841 p.) |
Disciplina |
547.593
547/.59/05 547/.593 |
Altri autori (Persone) |
RosowskyAndre
RenfroeBurt WattheyJeffrey W. H |
Collana | Chemistry of heterocyclic compounds |
Soggetto topico |
Azepines
Chemistry |
ISBN |
1-282-30195-0
9786612301957 0-470-18721-2 0-470-18873-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
AZEPINES; Contents; CHAPTER I. DIBENZAZEPINES AND OTHER TRICYCLIC AZEPINES; I. Introduction; II. 3,6,7-Systems; 1. Oxireno[d][2]benzazepines; 2. Benzo[b]cycloprop[d]azepines; 3. Benzo[d]cycloprop[b]azepines; III. 5,5,7-Systems; 1. Cyclopenta[c]tetrazolo[1,5-a]azepines; 2. 2,2a,3-Trithia(2a-Siv)-4a-azacyclopent[cd]azulenes; 3. Dipyrazolo[4,3-c:3',4'-e]azepines; 4. Thiazolo[2',3':2,3]imidazo[1,5-a]azepines; 5. Dipyrrolo[1,2-a:2',3'-d]azepines; 6. Azepino[2,1,7-cd]pyrrolizines; 7. Furo[3,2-c]pyrrolo[1,2-a]azepines; 8. Dithieno[2,3-e.'3',2'-e]azepines; IV. 5,6,7-Systems
1. Tetrazolo[5,1-a][2]benzazepines2. Tetrazolo[5,1-b][3]benzazepines; 3. 1,2,4-Triazolo[3,4-b][3]benzazepines; 4. Azepino[2,1-b]benzoxazoles; 5. Oxazolo[2,3-a][2]benzazepines; 6. Isothiazolo[5',4':4,5]pyrimido[1,2-a]azepines; 7. Azepino[2,l-b]benzothiazoles; 8. Isothiazolo[3,2,-b][3]benzazepines; 9. Thiazolo[2,3-a][2]benzazepines; 10. Thiazolo[2,3-b][3]benzazepines; 11. Thiazolo[3,2-b][2]benzazepines; 12. Thiazolo[3,2-a][1]benzazepines; 13. Azepino[2,1-b]benzoselenazoles; 14. Azepino[1,2-e]purines; 15. Azepino[2,1-f]purines; 16. Pyrazolo[3',4':4,5]pyrimido[1,2-a]azepines 17. 2a,4,9a-Triazabenz[c,d]azulenes18. Pyrido[3',2':4,5]imidazo[1,2-a]azepines; 19. Pyrido[3',4':4,5]irnidazo[1,2-a]azepines; 20. Azepino[1,2-a]benzimidazoles; 21. Imidazo[2,1-a][2]benzazepines; 22. Imidazo[2,1-b][3]benzazepines; 23. Imidazo[4,5-jk]benzazepines; 24. Pyrazolo[3,4-b]benzazepines; 25. Pyrazolo[3,4-c][1]benzazepines; 26. Pyrazolo[3,4-c][2]benzazepines; 27. Pyrazolo[4,3-d][2]benzazepines; 28. 1,3-Dioxolo[4,5-h][2]benzazepines; 29. 1,3-Dioxolo[4,5-h][3]benzazepines; 30. [1,3]Oxazino[3,2-a]pyrrolo[2,3-f]azepines; 31. Azepino[2,1,7-cd]indolizines 32. Pyrido[3',2':4,5]pyrrolo[2,3-c]azepines33. Pyrido[3',4':4,5]pyrrolo[2,3-c]azepines; 34. Azepino[1,2-a]indoles; 35. Azepino[2,1-i]indoles; 36. Azepino[2,3-b]indoles; 37. Azepino[3,2-b]indoles; 38. Azepino[3,4-b]indoles; 39. Azepino[3,2,l-hi]indoles; 40. Azepino[3,4,5-cd]indoles; 41. Azepino[4,3-b]indoles; 42. Azepino[4,3,2-cd]dindoles; 43. Azepino[4,5-b]indoles; 44. Azepino[5,4,3-cd]indoles; 45. Azepino[4,5-e]indoles; 46. Azepino[4,5-f]indoles; 47. Azepino[4,5-g]indoles; 48. Azepino[2,1-a]isoindoles; 49. Pyrrolo[l,2-a][1]benzazepines; 50. Pyrrolo[l,2-b][2]benzazepines 51. Pyrrolo[2,1-b][3]benzazepines52. Furo[2',3':4,5]pyrimido[1,2-a]azepines; 53. Benzofuro[2,3-b]azepines; 54. Benzofuro[2,3-c]azepines; 55. Benzofuro[3,2-b]azepines; 56. Benzofuro[3,2-c]azepines; 57. Furo[2,3-g]benzazepines; 58. Furo[3,2-g][1]benzazepines; 59. Furo[3,2-g][2]benzazepines; 60. Furo[3,2-i][1]benzazepines; 61. Furo[3,2-i][2]benzazepines; 62. Furo[3,4-c][1]benzazepines; 63. Thieno[2',3':4,5]pyrimido[1,2-a]azepines; 64. Thieno[4,3,2-ef][1]benzazepines; 65. [1]Benzothieno[2,3-c]azepines; 66. [1]Benzothieno[3,2-b]azepines; 67. [1]Benzothieno[3,2-c]azepines 68. Thieno[2,3-c][1]benzazepines |
Record Nr. | UNINA-9910643087203321 |
New York, : John Wiley and Sons, 1984 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Azepines . Part 1 [[electronic resource] /] / Jeffrey W.H. Watthey, James Stanton, Norton P. Peet; editor, Andre Rosowsky |
Pubbl/distr/stampa | New York, : John Wiley and Sons, 1984 |
Descrizione fisica | 1 online resource (841 p.) |
Disciplina |
547.593
547/.59/05 547/.593 |
Altri autori (Persone) |
RosowskyAndre
RenfroeBurt WattheyJeffrey W. H |
Collana | Chemistry of heterocyclic compounds |
Soggetto topico |
Azepines
Chemistry |
ISBN |
1-282-30195-0
9786612301957 0-470-18721-2 0-470-18873-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
AZEPINES; Contents; CHAPTER I. DIBENZAZEPINES AND OTHER TRICYCLIC AZEPINES; I. Introduction; II. 3,6,7-Systems; 1. Oxireno[d][2]benzazepines; 2. Benzo[b]cycloprop[d]azepines; 3. Benzo[d]cycloprop[b]azepines; III. 5,5,7-Systems; 1. Cyclopenta[c]tetrazolo[1,5-a]azepines; 2. 2,2a,3-Trithia(2a-Siv)-4a-azacyclopent[cd]azulenes; 3. Dipyrazolo[4,3-c:3',4'-e]azepines; 4. Thiazolo[2',3':2,3]imidazo[1,5-a]azepines; 5. Dipyrrolo[1,2-a:2',3'-d]azepines; 6. Azepino[2,1,7-cd]pyrrolizines; 7. Furo[3,2-c]pyrrolo[1,2-a]azepines; 8. Dithieno[2,3-e.'3',2'-e]azepines; IV. 5,6,7-Systems
1. Tetrazolo[5,1-a][2]benzazepines2. Tetrazolo[5,1-b][3]benzazepines; 3. 1,2,4-Triazolo[3,4-b][3]benzazepines; 4. Azepino[2,1-b]benzoxazoles; 5. Oxazolo[2,3-a][2]benzazepines; 6. Isothiazolo[5',4':4,5]pyrimido[1,2-a]azepines; 7. Azepino[2,l-b]benzothiazoles; 8. Isothiazolo[3,2,-b][3]benzazepines; 9. Thiazolo[2,3-a][2]benzazepines; 10. Thiazolo[2,3-b][3]benzazepines; 11. Thiazolo[3,2-b][2]benzazepines; 12. Thiazolo[3,2-a][1]benzazepines; 13. Azepino[2,1-b]benzoselenazoles; 14. Azepino[1,2-e]purines; 15. Azepino[2,1-f]purines; 16. Pyrazolo[3',4':4,5]pyrimido[1,2-a]azepines 17. 2a,4,9a-Triazabenz[c,d]azulenes18. Pyrido[3',2':4,5]imidazo[1,2-a]azepines; 19. Pyrido[3',4':4,5]irnidazo[1,2-a]azepines; 20. Azepino[1,2-a]benzimidazoles; 21. Imidazo[2,1-a][2]benzazepines; 22. Imidazo[2,1-b][3]benzazepines; 23. Imidazo[4,5-jk]benzazepines; 24. Pyrazolo[3,4-b]benzazepines; 25. Pyrazolo[3,4-c][1]benzazepines; 26. Pyrazolo[3,4-c][2]benzazepines; 27. Pyrazolo[4,3-d][2]benzazepines; 28. 1,3-Dioxolo[4,5-h][2]benzazepines; 29. 1,3-Dioxolo[4,5-h][3]benzazepines; 30. [1,3]Oxazino[3,2-a]pyrrolo[2,3-f]azepines; 31. Azepino[2,1,7-cd]indolizines 32. Pyrido[3',2':4,5]pyrrolo[2,3-c]azepines33. Pyrido[3',4':4,5]pyrrolo[2,3-c]azepines; 34. Azepino[1,2-a]indoles; 35. Azepino[2,1-i]indoles; 36. Azepino[2,3-b]indoles; 37. Azepino[3,2-b]indoles; 38. Azepino[3,4-b]indoles; 39. Azepino[3,2,l-hi]indoles; 40. Azepino[3,4,5-cd]indoles; 41. Azepino[4,3-b]indoles; 42. Azepino[4,3,2-cd]dindoles; 43. Azepino[4,5-b]indoles; 44. Azepino[5,4,3-cd]indoles; 45. Azepino[4,5-e]indoles; 46. Azepino[4,5-f]indoles; 47. Azepino[4,5-g]indoles; 48. Azepino[2,1-a]isoindoles; 49. Pyrrolo[l,2-a][1]benzazepines; 50. Pyrrolo[l,2-b][2]benzazepines 51. Pyrrolo[2,1-b][3]benzazepines52. Furo[2',3':4,5]pyrimido[1,2-a]azepines; 53. Benzofuro[2,3-b]azepines; 54. Benzofuro[2,3-c]azepines; 55. Benzofuro[3,2-b]azepines; 56. Benzofuro[3,2-c]azepines; 57. Furo[2,3-g]benzazepines; 58. Furo[3,2-g][1]benzazepines; 59. Furo[3,2-g][2]benzazepines; 60. Furo[3,2-i][1]benzazepines; 61. Furo[3,2-i][2]benzazepines; 62. Furo[3,4-c][1]benzazepines; 63. Thieno[2',3':4,5]pyrimido[1,2-a]azepines; 64. Thieno[4,3,2-ef][1]benzazepines; 65. [1]Benzothieno[2,3-c]azepines; 66. [1]Benzothieno[3,2-b]azepines; 67. [1]Benzothieno[3,2-c]azepines 68. Thieno[2,3-c][1]benzazepines |
Record Nr. | UNINA-9910830141903321 |
New York, : John Wiley and Sons, 1984 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Azepines . Part 1 [[electronic resource] /] / Jeffrey W.H. Watthey, James Stanton, Norton P. Peet; editor, Andre Rosowsky |
Pubbl/distr/stampa | New York, : John Wiley and Sons, 1984 |
Descrizione fisica | 1 online resource (841 p.) |
Disciplina |
547.593
547/.59/05 547/.593 |
Altri autori (Persone) |
RosowskyAndre
RenfroeBurt WattheyJeffrey W. H |
Collana | Chemistry of heterocyclic compounds |
Soggetto topico |
Azepines
Chemistry |
ISBN |
1-282-30195-0
9786612301957 0-470-18721-2 0-470-18873-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
AZEPINES; Contents; CHAPTER I. DIBENZAZEPINES AND OTHER TRICYCLIC AZEPINES; I. Introduction; II. 3,6,7-Systems; 1. Oxireno[d][2]benzazepines; 2. Benzo[b]cycloprop[d]azepines; 3. Benzo[d]cycloprop[b]azepines; III. 5,5,7-Systems; 1. Cyclopenta[c]tetrazolo[1,5-a]azepines; 2. 2,2a,3-Trithia(2a-Siv)-4a-azacyclopent[cd]azulenes; 3. Dipyrazolo[4,3-c:3',4'-e]azepines; 4. Thiazolo[2',3':2,3]imidazo[1,5-a]azepines; 5. Dipyrrolo[1,2-a:2',3'-d]azepines; 6. Azepino[2,1,7-cd]pyrrolizines; 7. Furo[3,2-c]pyrrolo[1,2-a]azepines; 8. Dithieno[2,3-e.'3',2'-e]azepines; IV. 5,6,7-Systems
1. Tetrazolo[5,1-a][2]benzazepines2. Tetrazolo[5,1-b][3]benzazepines; 3. 1,2,4-Triazolo[3,4-b][3]benzazepines; 4. Azepino[2,1-b]benzoxazoles; 5. Oxazolo[2,3-a][2]benzazepines; 6. Isothiazolo[5',4':4,5]pyrimido[1,2-a]azepines; 7. Azepino[2,l-b]benzothiazoles; 8. Isothiazolo[3,2,-b][3]benzazepines; 9. Thiazolo[2,3-a][2]benzazepines; 10. Thiazolo[2,3-b][3]benzazepines; 11. Thiazolo[3,2-b][2]benzazepines; 12. Thiazolo[3,2-a][1]benzazepines; 13. Azepino[2,1-b]benzoselenazoles; 14. Azepino[1,2-e]purines; 15. Azepino[2,1-f]purines; 16. Pyrazolo[3',4':4,5]pyrimido[1,2-a]azepines 17. 2a,4,9a-Triazabenz[c,d]azulenes18. Pyrido[3',2':4,5]imidazo[1,2-a]azepines; 19. Pyrido[3',4':4,5]irnidazo[1,2-a]azepines; 20. Azepino[1,2-a]benzimidazoles; 21. Imidazo[2,1-a][2]benzazepines; 22. Imidazo[2,1-b][3]benzazepines; 23. Imidazo[4,5-jk]benzazepines; 24. Pyrazolo[3,4-b]benzazepines; 25. Pyrazolo[3,4-c][1]benzazepines; 26. Pyrazolo[3,4-c][2]benzazepines; 27. Pyrazolo[4,3-d][2]benzazepines; 28. 1,3-Dioxolo[4,5-h][2]benzazepines; 29. 1,3-Dioxolo[4,5-h][3]benzazepines; 30. [1,3]Oxazino[3,2-a]pyrrolo[2,3-f]azepines; 31. Azepino[2,1,7-cd]indolizines 32. Pyrido[3',2':4,5]pyrrolo[2,3-c]azepines33. Pyrido[3',4':4,5]pyrrolo[2,3-c]azepines; 34. Azepino[1,2-a]indoles; 35. Azepino[2,1-i]indoles; 36. Azepino[2,3-b]indoles; 37. Azepino[3,2-b]indoles; 38. Azepino[3,4-b]indoles; 39. Azepino[3,2,l-hi]indoles; 40. Azepino[3,4,5-cd]indoles; 41. Azepino[4,3-b]indoles; 42. Azepino[4,3,2-cd]dindoles; 43. Azepino[4,5-b]indoles; 44. Azepino[5,4,3-cd]indoles; 45. Azepino[4,5-e]indoles; 46. Azepino[4,5-f]indoles; 47. Azepino[4,5-g]indoles; 48. Azepino[2,1-a]isoindoles; 49. Pyrrolo[l,2-a][1]benzazepines; 50. Pyrrolo[l,2-b][2]benzazepines 51. Pyrrolo[2,1-b][3]benzazepines52. Furo[2',3':4,5]pyrimido[1,2-a]azepines; 53. Benzofuro[2,3-b]azepines; 54. Benzofuro[2,3-c]azepines; 55. Benzofuro[3,2-b]azepines; 56. Benzofuro[3,2-c]azepines; 57. Furo[2,3-g]benzazepines; 58. Furo[3,2-g][1]benzazepines; 59. Furo[3,2-g][2]benzazepines; 60. Furo[3,2-i][1]benzazepines; 61. Furo[3,2-i][2]benzazepines; 62. Furo[3,4-c][1]benzazepines; 63. Thieno[2',3':4,5]pyrimido[1,2-a]azepines; 64. Thieno[4,3,2-ef][1]benzazepines; 65. [1]Benzothieno[2,3-c]azepines; 66. [1]Benzothieno[3,2-b]azepines; 67. [1]Benzothieno[3,2-c]azepines 68. Thieno[2,3-c][1]benzazepines |
Record Nr. | UNINA-9910841545903321 |
New York, : John Wiley and Sons, 1984 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Dihydrofolate reductase overproductionidentified by flow cytometry using a fluorescent methotrexate analogue / [by] A. Rosowsky [et al.]. Berlin, 1983, p. 475-479 |
Altri autori (Persone) | Rosowsky, Andre |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | und |
Record Nr. | UNINA-990002249090403321 |
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Seven-membered heterocyclic compounds containing oxygen and sulfur [[electronic resource] /] / edited by Andre Rosowsky |
Autore | Rosowsky Andre |
Edizione | [99th ed.] |
Pubbl/distr/stampa | New York, : Wiley-Interscience, 1972 |
Descrizione fisica | 1 online resource (982 p.) |
Disciplina |
547.592
547/.59/05 547/.592 |
Altri autori (Persone) | RosowskyAndre |
Collana | Chemistry of heterocyclic compounds |
Soggetto topico |
Oxepins
Thiepins |
ISBN |
1-282-30171-3
9786612301711 0-470-18696-8 0-470-18845-6 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
THE CHEMISTRY OF HETEROCYCLIC COMPOUNDS A SERIES OF MONOGRAPHS; Preface; Contents; Tables; I. Oxepins and Reduced Oxepins; A. OXEPINS; 1. Theoretical Interest; 2. Preparation; 3. Physical Properties; a. Infrared Absorption; b. Ultraviolet Absorption; c. Nuclear Magnetic Resonance; d. Thermodynamic Properties; 4. Chemical Reactions; a. Addendum; B. DIHYDROOXEPINS; 1. Introduction; 2. Preparation; 3. Physical Properties; a. Infrared Absorption; b. Ultraviolet Absorption; c. Nuclear Magnetic Resonance; 4. Chemical Reactions; C. TETRAHYDROOXEPINS; 1. Introduction; 2. Preparation
3. Physical Propertiesa. Infrared Absorption; b. Nuclear Magnetic Resonance; 4. Chemical Reactions; D. HEXAHYDROOXEPINS (OXEPANS); 1. Preparation; a. Hexamethylene Oxide; b. Substituted Oxepans; (1) Ring Closure Reactions; (2) Ring Expansion Reactions; (3) Two-Component Reactions; 2. Physical Properties of Hexamethylene Oxide; 3. Chemical Reactions of Hexamethylene Oxide; 4. Preparation and Reactions of Cyclic Acetals, Ketals, and Related Compounds; E. TABLES; I-1. Oxepins and Reduced Oxepins; F. REFERENCES; II. Oxepin Ring Systems Containing Two Rings; A. FUSED RINGS SYSTEMS 1. 2-Oxabicyclo[5.1.0]octanes2. 2-Oxabicyclo[5.2.0]nonanes; 3. 2H-Cyclopent[b]oxepins; 4. 2H-Cyclopent[d]oxepins; 5. Furo[3,4-b]oxepins; 6. Furo[3,4-d]oxepins; 7. 2H-Oxepino[2,3-b]pyrroles; 8. Thieno[3,4-d]oxepins; 9.1-Benzoxepins; a. Synthesis, Chemical Reactions, and Physical Properties of the Parent Compound; b. Synthesis and Chemical Reactions of Dihydro-l-benzoxepins; c. Synthesis and Chemical Reactions of Tetrahydro-l- benzoxepins; d. Synthesis and Chemical Reactions of Other Reduced 1-Benzoxepins; e. Physicochemical Properties of 2,3,4,5-Tetrahydro-1- benzoxepins; 10.2-Benzoxepins 11. 3-BenzoxepinsB. SPIRANS; 1. 1,7-Dioxaspiro[5.6]dodecanes; 2. 1,4,6-Trioxaspiro[4.6]undecanes; C. BRIDGED SYSTEMS; 1. 2-Oxabicyclo[3.2.2]nonanes; 2. 3-Oxabicyclo[3.2.2]nonanes; 3. 9-Oxabicyclo[3.3.2]decanes; 4. 11-Oxabicyclo[4.4.1]undecanes; a. Partly or Fully Saturated Derivatives; b. 1,6-Oxido[10]annulenes; 5. 3-Oxa-6,7-dithiabicyclo[3.2.2]nonanes; D. TABLES; II-1. Uv Data and Bromination Rate of 2,3,4,5-Tetrahydro-l-benzoxepins and Lower Ring Homologs; II-2. Solvolysis Kinetics of 7-Chloromethyl-2,3,4,5-tetrahydro-l- benzoxepin and Lower Ring Homologs II-3. Uv Data and Bromination Rate of 2,3,4,5-Tetrahydro-l- benzoxepin-2-carboxylic Acid and Lower Ring HomologsII-4. Uv Data and Molecular Geometry of 2,3,4,5-Tetrahydro-2-(N,N-dimethylamino)methyl-1-benzoxepin Methobromide and Lower Ring Homologs; II-5. l-Benzoxepins; II-6. 2-Benzoxepins; II-7. 3-Benzoxepins; E. REFERENCES; III. Oxepin Ring Systems Containing Three Rings; A. FUSED RING SYSTEMS; 1. Cyclopenta[5.6]pyrano[4,3-b]oxepins; 2. 8H-1,3-Dioxolo[4,5-h][3]benzoxepins; 3. Dibenz[b,d]oxepins; 4. Dibenz[b,e]oxepins; 5. Dibenz[b,f]oxepins; 6. Dibenz[c,e]oxepins a. Dibenz[c,e]oxepin-5,7-diones (Diphenic Anhydrides) |
Record Nr. | UNINA-9910144281403321 |
Rosowsky Andre | ||
New York, : Wiley-Interscience, 1972 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Seven-membered heterocyclic compounds containing oxygen and sulfur [[electronic resource] /] / edited by Andre Rosowsky |
Autore | Rosowsky Andre |
Edizione | [99th ed.] |
Pubbl/distr/stampa | New York, : Wiley-Interscience, 1972 |
Descrizione fisica | 1 online resource (982 p.) |
Disciplina |
547.592
547/.59/05 547/.592 |
Altri autori (Persone) | RosowskyAndre |
Collana | Chemistry of heterocyclic compounds |
Soggetto topico |
Oxepins
Thiepins |
ISBN |
1-282-30171-3
9786612301711 0-470-18696-8 0-470-18845-6 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
THE CHEMISTRY OF HETEROCYCLIC COMPOUNDS A SERIES OF MONOGRAPHS; Preface; Contents; Tables; I. Oxepins and Reduced Oxepins; A. OXEPINS; 1. Theoretical Interest; 2. Preparation; 3. Physical Properties; a. Infrared Absorption; b. Ultraviolet Absorption; c. Nuclear Magnetic Resonance; d. Thermodynamic Properties; 4. Chemical Reactions; a. Addendum; B. DIHYDROOXEPINS; 1. Introduction; 2. Preparation; 3. Physical Properties; a. Infrared Absorption; b. Ultraviolet Absorption; c. Nuclear Magnetic Resonance; 4. Chemical Reactions; C. TETRAHYDROOXEPINS; 1. Introduction; 2. Preparation
3. Physical Propertiesa. Infrared Absorption; b. Nuclear Magnetic Resonance; 4. Chemical Reactions; D. HEXAHYDROOXEPINS (OXEPANS); 1. Preparation; a. Hexamethylene Oxide; b. Substituted Oxepans; (1) Ring Closure Reactions; (2) Ring Expansion Reactions; (3) Two-Component Reactions; 2. Physical Properties of Hexamethylene Oxide; 3. Chemical Reactions of Hexamethylene Oxide; 4. Preparation and Reactions of Cyclic Acetals, Ketals, and Related Compounds; E. TABLES; I-1. Oxepins and Reduced Oxepins; F. REFERENCES; II. Oxepin Ring Systems Containing Two Rings; A. FUSED RINGS SYSTEMS 1. 2-Oxabicyclo[5.1.0]octanes2. 2-Oxabicyclo[5.2.0]nonanes; 3. 2H-Cyclopent[b]oxepins; 4. 2H-Cyclopent[d]oxepins; 5. Furo[3,4-b]oxepins; 6. Furo[3,4-d]oxepins; 7. 2H-Oxepino[2,3-b]pyrroles; 8. Thieno[3,4-d]oxepins; 9.1-Benzoxepins; a. Synthesis, Chemical Reactions, and Physical Properties of the Parent Compound; b. Synthesis and Chemical Reactions of Dihydro-l-benzoxepins; c. Synthesis and Chemical Reactions of Tetrahydro-l- benzoxepins; d. Synthesis and Chemical Reactions of Other Reduced 1-Benzoxepins; e. Physicochemical Properties of 2,3,4,5-Tetrahydro-1- benzoxepins; 10.2-Benzoxepins 11. 3-BenzoxepinsB. SPIRANS; 1. 1,7-Dioxaspiro[5.6]dodecanes; 2. 1,4,6-Trioxaspiro[4.6]undecanes; C. BRIDGED SYSTEMS; 1. 2-Oxabicyclo[3.2.2]nonanes; 2. 3-Oxabicyclo[3.2.2]nonanes; 3. 9-Oxabicyclo[3.3.2]decanes; 4. 11-Oxabicyclo[4.4.1]undecanes; a. Partly or Fully Saturated Derivatives; b. 1,6-Oxido[10]annulenes; 5. 3-Oxa-6,7-dithiabicyclo[3.2.2]nonanes; D. TABLES; II-1. Uv Data and Bromination Rate of 2,3,4,5-Tetrahydro-l-benzoxepins and Lower Ring Homologs; II-2. Solvolysis Kinetics of 7-Chloromethyl-2,3,4,5-tetrahydro-l- benzoxepin and Lower Ring Homologs II-3. Uv Data and Bromination Rate of 2,3,4,5-Tetrahydro-l- benzoxepin-2-carboxylic Acid and Lower Ring HomologsII-4. Uv Data and Molecular Geometry of 2,3,4,5-Tetrahydro-2-(N,N-dimethylamino)methyl-1-benzoxepin Methobromide and Lower Ring Homologs; II-5. l-Benzoxepins; II-6. 2-Benzoxepins; II-7. 3-Benzoxepins; E. REFERENCES; III. Oxepin Ring Systems Containing Three Rings; A. FUSED RING SYSTEMS; 1. Cyclopenta[5.6]pyrano[4,3-b]oxepins; 2. 8H-1,3-Dioxolo[4,5-h][3]benzoxepins; 3. Dibenz[b,d]oxepins; 4. Dibenz[b,e]oxepins; 5. Dibenz[b,f]oxepins; 6. Dibenz[c,e]oxepins a. Dibenz[c,e]oxepin-5,7-diones (Diphenic Anhydrides) |
Record Nr. | UNINA-9910830918803321 |
Rosowsky Andre | ||
New York, : Wiley-Interscience, 1972 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Seven-membered heterocyclic compounds containing oxygen and sulfur [[electronic resource] /] / edited by Andre Rosowsky |
Autore | Rosowsky Andre |
Edizione | [99th ed.] |
Pubbl/distr/stampa | New York, : Wiley-Interscience, 1972 |
Descrizione fisica | 1 online resource (982 p.) |
Disciplina |
547.592
547/.59/05 547/.592 |
Altri autori (Persone) | RosowskyAndre |
Collana | Chemistry of heterocyclic compounds |
Soggetto topico |
Oxepins
Thiepins |
ISBN |
1-282-30171-3
9786612301711 0-470-18696-8 0-470-18845-6 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
THE CHEMISTRY OF HETEROCYCLIC COMPOUNDS A SERIES OF MONOGRAPHS; Preface; Contents; Tables; I. Oxepins and Reduced Oxepins; A. OXEPINS; 1. Theoretical Interest; 2. Preparation; 3. Physical Properties; a. Infrared Absorption; b. Ultraviolet Absorption; c. Nuclear Magnetic Resonance; d. Thermodynamic Properties; 4. Chemical Reactions; a. Addendum; B. DIHYDROOXEPINS; 1. Introduction; 2. Preparation; 3. Physical Properties; a. Infrared Absorption; b. Ultraviolet Absorption; c. Nuclear Magnetic Resonance; 4. Chemical Reactions; C. TETRAHYDROOXEPINS; 1. Introduction; 2. Preparation
3. Physical Propertiesa. Infrared Absorption; b. Nuclear Magnetic Resonance; 4. Chemical Reactions; D. HEXAHYDROOXEPINS (OXEPANS); 1. Preparation; a. Hexamethylene Oxide; b. Substituted Oxepans; (1) Ring Closure Reactions; (2) Ring Expansion Reactions; (3) Two-Component Reactions; 2. Physical Properties of Hexamethylene Oxide; 3. Chemical Reactions of Hexamethylene Oxide; 4. Preparation and Reactions of Cyclic Acetals, Ketals, and Related Compounds; E. TABLES; I-1. Oxepins and Reduced Oxepins; F. REFERENCES; II. Oxepin Ring Systems Containing Two Rings; A. FUSED RINGS SYSTEMS 1. 2-Oxabicyclo[5.1.0]octanes2. 2-Oxabicyclo[5.2.0]nonanes; 3. 2H-Cyclopent[b]oxepins; 4. 2H-Cyclopent[d]oxepins; 5. Furo[3,4-b]oxepins; 6. Furo[3,4-d]oxepins; 7. 2H-Oxepino[2,3-b]pyrroles; 8. Thieno[3,4-d]oxepins; 9.1-Benzoxepins; a. Synthesis, Chemical Reactions, and Physical Properties of the Parent Compound; b. Synthesis and Chemical Reactions of Dihydro-l-benzoxepins; c. Synthesis and Chemical Reactions of Tetrahydro-l- benzoxepins; d. Synthesis and Chemical Reactions of Other Reduced 1-Benzoxepins; e. Physicochemical Properties of 2,3,4,5-Tetrahydro-1- benzoxepins; 10.2-Benzoxepins 11. 3-BenzoxepinsB. SPIRANS; 1. 1,7-Dioxaspiro[5.6]dodecanes; 2. 1,4,6-Trioxaspiro[4.6]undecanes; C. BRIDGED SYSTEMS; 1. 2-Oxabicyclo[3.2.2]nonanes; 2. 3-Oxabicyclo[3.2.2]nonanes; 3. 9-Oxabicyclo[3.3.2]decanes; 4. 11-Oxabicyclo[4.4.1]undecanes; a. Partly or Fully Saturated Derivatives; b. 1,6-Oxido[10]annulenes; 5. 3-Oxa-6,7-dithiabicyclo[3.2.2]nonanes; D. TABLES; II-1. Uv Data and Bromination Rate of 2,3,4,5-Tetrahydro-l-benzoxepins and Lower Ring Homologs; II-2. Solvolysis Kinetics of 7-Chloromethyl-2,3,4,5-tetrahydro-l- benzoxepin and Lower Ring Homologs II-3. Uv Data and Bromination Rate of 2,3,4,5-Tetrahydro-l- benzoxepin-2-carboxylic Acid and Lower Ring HomologsII-4. Uv Data and Molecular Geometry of 2,3,4,5-Tetrahydro-2-(N,N-dimethylamino)methyl-1-benzoxepin Methobromide and Lower Ring Homologs; II-5. l-Benzoxepins; II-6. 2-Benzoxepins; II-7. 3-Benzoxepins; E. REFERENCES; III. Oxepin Ring Systems Containing Three Rings; A. FUSED RING SYSTEMS; 1. Cyclopenta[5.6]pyrano[4,3-b]oxepins; 2. 8H-1,3-Dioxolo[4,5-h][3]benzoxepins; 3. Dibenz[b,d]oxepins; 4. Dibenz[b,e]oxepins; 5. Dibenz[b,f]oxepins; 6. Dibenz[c,e]oxepins a. Dibenz[c,e]oxepin-5,7-diones (Diphenic Anhydrides) |
Record Nr. | UNINA-9910841260403321 |
Rosowsky Andre | ||
New York, : Wiley-Interscience, 1972 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|