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1. |
Record Nr. |
UNINA9910309458103321 |
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Autore |
Voza, Pasquale |
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Titolo |
Pasolini e la dittatura del presente / Pasquale Voza |
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Pubbl/distr/stampa |
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San Cesario di Lecce : Manni, 2016 |
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ISBN |
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Descrizione fisica |
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Collana |
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Disciplina |
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Locazione |
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Collocazione |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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2. |
Record Nr. |
UNISA996395695203316 |
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Autore |
Bretnor Thomas <fl. 1607-1618.> |
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Titolo |
Bretnor. 1607 [[electronic resource] ] : A new almanacke and prognostication for the yeare of our Lord God, M. DC. VII. being the third from the leape yeare. Uery necessary for all [men] especially for marchent, mariners, ch[i]rugians, husbandmen and trauellers. Calculated and composed according to art, for the latitude and meridian of the honourable citty of London, [and] may very well serue all the south parts of Great Brittaine. / / By Thomas Bretnor . |
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Pubbl/distr/stampa |
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[London], : Imprinted at London for the Company of Stationers., [1607] |
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Descrizione fisica |
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[48] p. : ill. (woodcut), tables |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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3. |
Record Nr. |
UNINA9911019862503321 |
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Autore |
Breslow David Samuel <1916-> |
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Titolo |
Multi-sulfur and sulfur and oxygen five- and six-membered heterocycles . Part one / / David S. Breslow, Herman Skolnik |
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Pubbl/distr/stampa |
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New York, : Interscience, 1966 |
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ISBN |
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9786612301605 |
9781282301603 |
1282301608 |
9780470186824 |
0470186828 |
9780470188323 |
0470188324 |
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Edizione |
[99th ed.] |
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Descrizione fisica |
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1 online resource (635 p.) |
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Collana |
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Chemistry of heterocyclic compounds ; ; 21/1 |
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Altri autori (Persone) |
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Disciplina |
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Soggetti |
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Organosulfur compounds |
Heterocyclic compounds |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Nota di contenuto |
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MULTI-SULFUR AND SULFUR AND OXYGEN FIVE- AND SIXMEMBERED HETEROCYCLES; CONTENTS OF PART ONE; 1. C2O2S Ring Systems; I. C2O2S 1, 3, 2-Dioxathiolane and 1, 3, 2-Dioxathiole; A. Sulfite Esters of 1, 2-Glycols; 1. Preparation; 2. Structure and Physical Properties; 3. Reactions; 4. Uses; B. Sulfate Esters of 1, 2-Glycols; 1. Preparation; 2. Structure and Reactions; C. Sulfate Esters of Enediols; D. 1, 3, 2-Dioxathiolan-4-one 2-Oxides; II. C4-C2O2S 2, 4-Dioxa-3-thiabicyclo[3. 2. 0]heptane; III. C2O2S-C2O2S 1, 3, 2-Dioxathiolo[1, 3, 2]dioxathiole Glyoxal Sulfate |
IV. C2O2S-C4O Furo[3, 4-d]-l, 3, 2-dioxathioleV. C2O2S-C4S Thieno[3, 4-d]-1, 3, 2-dioxathiole; VI. C2O2S-C5 3aH-Cyclopenta-1, 3, 2-dioxathiole; VII. C2O2S-C5O 4H-Pyrano[3, 4-d]-1, 3, 2-dioxathiole; VIII. C2O2S-C6 1, 3, 2-Benzodioxathiole; A. Sulfite Esters; B. Sulfate Esters; IX. C2O2S-C7 4H-Cyclohepta-1, 3, 2-dioxathiole; X. C2O2S-C4O-C4O 1, 7, 11, 13-Tetraoxa-12-thiadispiro-[4. 0. 4. 3]trideca-3, |
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9-diene-2, 8-dione; XI. C2O2S-C4N-C5N 6H-Cyclohepta-1, 3, 2-dioxathiol-4, 8-imine; XII. C2O2S-C5-C6 8H-Indeno[1, 2-d}-1, 3, 2-dioxathiole |
XIII. C2O2S-C4O2-C50 4H, 6H-1, 3, 2-Dioxathiolo[4, 5]-pyrano[3, 2-d]-m-dioxinXIV. C2O2S-C6C6; A. Naphtho[1, 2-d}-1, 3, 2-dioxathiole; B. Naphtho[2, 3-d]-1, 3, 2-dioxathiole; XV. C2O2S-C6-C6-C6; A. Anthra[1, 2-d]-1, 3, 2-dioxathiole; 1. Sulfite Esters; 2. Sulfate Esters; B. Anthra[2, 3-d]-1, 3, 2-dioxathiole; C. Phenanthro[9, 10-d]-1, 3, 2-dioxathiole; XVI. C2O2S-C4N-C4N-C9O2 [1, 3, 2]Dioxathiolo-[4', 5' : 8, 9][1, 6]dioxacycloundeca[2, 3, 4-gh]-pyrrolizine; XVII. C2O2S-C4N-C4N-C10O2 Spiro[1, 6]dioxacyclododeca-[2, 3, 4-gh]-pyrrolizine-9(8H), 4'-[ 1, 3, 2]-dioxathiolane |
XVIII. C2O2S-C5-C6-C6-C6A. Cyclopenta[1, 2]phenanthro[4, 4a-d][1, 3, 2]-dioxathiole; B. Cyclopenta[1, 2]phenanthro[1, 10a-d][1, 3, 2]-dioxathiole; XIX. C2O2S-C6-C6-C6-C6; A. Chryseno[5, 6-d]-1, 3, 2-dioxathiole; B. 4, 9-o-Benzenonaphtho[2, 3-d]-1, 3, 2-dioxathiole; XX. C2O2S-C4O-C4O-C5-C6-C6 3H, 9H-11b, 13a-Epoxycyclopenta[1, 2]phenanthro[4, 4a-d][1, 3, 2]dioxathiole; 2. C2OS2 Ring Systems; I. 1, 2, 5-Oxadithia Compounds; A. C2OS2 1, 2, 5-Oxadithiolane; B. C2OS2-C4SThieno[3, 4-c][1, 2, 5]oxadithiole; C. C2OS2-C6 2, 1, 3-Benzoxadithiole; D. C2OS2-C6-C6 Naphth[1, 2-c][1, 2, 5]oxadithiole |
II. 1, 3, 4-Oxadithia CompoundsC2OS2 1, 3, 4-Oxadithiolane; 3. C2S3 Ring Systems; I. 1, 2, 3-Trithia Compounds; A. C2S3 1,2,3-Trithiole; B. C2S3-C6 Benzotrithiole; C. C2S3-C4N2-C6 Trithiolo[4, 5-b]quinoxaline; II. 1, 2, 4-Trithia Compounds; A. C2S3 1, 2, 4-Trithiolane; B. Spiro Derivatives of 1, 2, 4-Trithiolane; 4. C3OS Ring Systems; I. 1, 2-Oxathia Compounds; A. C3OS 5H-1, 2-Oxathiole, 3H-1, 2-Oxathiole, and 1, 2-Oxathiolane; 1. 3H-1, 2-Oxathiole; 2. 5H-1, 2-Oxathiole; 3. 1, 2-Oxathiolane; a. 1, 2-Oxathiolane 2, 2-Dioxide; (1) Preparation; (a) From 3-Chloroalkanesulfonic Acids |
(b) From 3-Hydroxyalkanesulphonic Acids |
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Sommario/riassunto |
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Chemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus. |
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