【精品分享】Name Reactions in Heterocyclic Chemistry

Name Reactions in Heterocyclic ChemistryEdited by
Jie-Jack Li
Pfizer Global Research & Development
Scientific Editor:
E. J. Corey
Harvard University
Copyright @2005 by John Wiley & Sons. Inc. All rights reserved.
IN 0-471-30215-5

Table of Contents
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 Paternc-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
2.3 Hofmann-Loffler-Freytag reaction
Knorr and Paal-Knorr pyrrole syntheses
Chapter 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 Gasan 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-BCnary fixan synthesis
4.2 Paal-Knorr furan synthesis
Chapter 5 Thiophenes
5.1 Fiesselmann thiophene synthesis
5.2 Gewald aminothiophene synthesis
5.3 Hinerg synthesis of thiophene derivatives
5.4 Paal thiophene synthesis
Hinerg synthesis of thiophene derivatives
Chapter 6 Oxazoles and Isoxazoles
6.1 Claisen isoxazole synthesis
6.2 Comforth 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
Chapter 8 Pyridines
Chapter 9 Quinolines and Isoquinolines
Chapter 10 Other Six-Membered Heterocycles
10.1 Algar-Flynn-Oyamada reaction
10.2 Beirut reaction
10.3 Biginelli reaction
10.4 Kostanecki-Robinson reaction
10.5 Pinner pyrimidine synthesis
10.6 von Richter cinnoline reaction

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