LEADER 00764nam0-22002771i-450- 001 990000959280403321 035 $a000095928 035 $aFED01000095928 035 $a(Aleph)000095928FED01 035 $a000095928 100 $a--------d--------km-y0itay50------ba 101 0 $aeng 200 1 $a<>Development of Mathematics$fby E.T. Bell 205 $a2nd ed. 210 $aNew York [etc.]$cMcGraw-Hill$d1945 610 0 $aStoria della matematica 676 $a509 700 1$aBell,$bEric Temple$f<1883-1960>$028647 801 0$aIT$bUNINA$gRICA$2UNIMARC 901 $aBK 912 $a990000959280403321 952 $a6B-009$b388$fFI1 952 $a6B-009.001$b560$fFI1 959 $aFI1 996 $aDevelopment of Mathematics$9345361 997 $aUNINA LEADER 05338nam 22006494a 450 001 9910830429203321 005 20230617031007.0 010 $a1-280-27303-8 010 $a9786610273034 010 $a0-470-35202-7 010 $a0-471-70414-8 010 $a0-471-70415-6 035 $a(CKB)1000000000018994 035 $a(EBL)221302 035 $a(OCoLC)123417691 035 $a(SSID)ssj0000207813 035 $a(PQKBManifestationID)11194285 035 $a(PQKBTitleCode)TC0000207813 035 $a(PQKBWorkID)10238115 035 $a(PQKB)11120009 035 $a(MiAaPQ)EBC221302 035 $a(EXLCZ)991000000000018994 100 $a20040518d2005 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aName reactions in heterocyclic chemistry$b[electronic resource] /$fedited by Jie-Jack Li 210 $aHoboken, N.J. $cWiley-Interscience$dc2005 215 $a1 online resource (579 p.) 225 1 $aComprehensive Name Reactions ;$vv.3 300 $aDescription based upon print version of record. 311 $a0-471-30215-5 320 $aIncludes bibliographical references and index. 327 $aName Reactions in Heterocyclic Chemistry; Table of Contents; Foreword; Preface; Acronyms and abbreviations; PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES; Chapter 1 Epoxides and Aziridines; 1.1 Corey-Chaykovsky reaction; 1.2 Darzens glycidic ester condensation; 1.3 Hoch-Campbell aziridine synthesis; 1.4 Jacobsen-Katsuki epoxidation; 1.5 Paterno-Buchi reaction; 1.6 Sharpless-Katsuki epoxidation; 1.7 Wenker aziridine synthesis; PART 2 FIVE-MEMBERED HETEROCYCLES; Chapter 2 Pyrroles and Pyrrolidines; 2.1 Barton-Zard reaction; 2.2 Knorr and Paal-Knorr pyrrole syntheses 327 $a2.3 Hofmann-Loffler-Freytag reactionChapter 3 Indoles; 3.1 Bartoli indole synthesis; 3.2 Batcho-Leimgruber indole synthesis; 3.3 Bucherer carbazole synthesis; 3.4 Fischer indole synthesis; 3.5 Gassman indole synthesis; 3.6 Graebe-Ullman carbazole synthesis; 3.7 Hegedus indole synthesis; 3.8 Madelung indole synthesis; 3.9 Nenitzescu indole synthesis; 3.10 Reissert indole synthesis; Chapter 4 Furans; 4.1 Feist-Benary furan synthesis; 4.2 Paal-Knorr furan synthesis; Chapter 5 Thiophenes; 5.1 Fiesselmann thiophene synthesis; 5.2 Gewald aminothiophene synthesis 327 $a5.3 Hinsberg synthesis of thiophene derivatives5.4 Paal thiophene synthesis; Chapter 6 Oxazoles and Isoxazoles; 6.1 Claisen isoxazole synthesis; 6.2 Cornforth rearrangement; 6.3 Erlenmeyer-Plochl azlactone synthesis; 6.4 Fischer oxazole synthesis; 6.5 Meyers oxazoline method; 6.6 Robinson-Gabriel synthesis; 6.7 van Leusen oxazole Synthesis; Chapter 7 Other Five-Membered Heterocycles; 7.1 Auwers flavone synthesis; 7.2 Bucherer-Bergs reaction; 7.3 Cook-Heilbron 5-amino-thiazole synthesis; 7.4 Hurd-Mori 1,2,3-thiadiazole synthesis; 7.5 Knorr pyrazole synthesis; PART 3 SIX-MEMBERED HETEROCYCLES 327 $aChapter 8 Pyridines8.1 Preparation via condensation reactions; 8.1.1 Hantzsch (dihydro)-pyridine synthesis; 8.1.1.1 Description; 8.1.1.2 Historical perspective; 8.1.1.3 Mechanism; 8.1.1.4 Variations; 8.1.1.4.1 Guareschi-Thorpe pyridine synthesis; 8.1.1.4.2 Chichibabin (Tschitschibabin) pyridine synthesis; 8.1.1.4.3 Bohlmann-Rahtz pyridine synthesis; 8.1.1.4.4 Krohnke pyridine synthesis; 8.1.1.4.5 Petrenko-Kritschenko piperidone synthesis; 8.1.1.5 Improvements or modifications; 8.1.1.6 Experimental; 8.1.1.6.1 Three-component coupling; 8.1.1.6.2 Two-component coupling; 8.1.1.7 References 327 $a8.2 Preparation via cycloaddition reactions8.2.1 Boger reaction; 8.3 Preparation via rearrangement reactions; 8.3.1 Boekelheide reaction; 8.3.2 Ciamician-Dennstedt rearrangement; 8.4 Zincke reaction; Chapter 9 Quinolines and Isoquinolines; 9.1 Bischler-Napieralski reaction; 9.2 Camps quinoline synthesis; 9.3 Combes quinoline synthesis; 9.4 Conrad-Limpach reaction; 9.5 Doebner quinoline synthesis; 9.6 Friedlander synthesis; 9.7 Gabriel-Colman rearrangement; 9.8 Gould-Jacobs reaction; 9.9 Knorr quinoline synthesis; 9.10 Meth-Cohn quinoline synthesis; 9.11 Pfitzinger quinoline synthesis 327 $a9.12 Pictet-Gams isoquinoline synthesis 330 $aCovers important name reactions relevant to heterocyclic chemistry The field of heterocyclic chemistry has long presented a special challenge for chemists. Because of the enormous amount and variety of information, it is often a difficult topic to cover for undergraduate and graduate chemistry students, even in simplified form. Yet the chemistry of heterocyclic compounds and methods for their synthesis form the bedrock of modern medicinal chemical and pharmaceutical research. Thus there is a great need for high quality, up-to-date, and authoritative books on heterocyclic synthesis helpful to 410 0$aComprehensive Name Reactions 606 $aHeterocyclic chemistry 606 $aChemical reactions 615 0$aHeterocyclic chemistry. 615 0$aChemical reactions. 676 $a547.59 676 $a547.590459 701 $aLi$b Jie Jack$0440094 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830429203321 996 $aName reactions in heterocyclic chemistry$93995394 997 $aUNINA