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The third edition contains major improvements over the previous two editions. I have updated references. Each reaction is now supplemented with two to three representative examples in synthesis to showcase its synthetic utility. As Emil Fi-scher stated:“Science is not an abstraction; but as a product of human endeavor it is inseparably bound up in its development with the personalities and fortunes of those who dedicate themselves to it .” To that end, I added biographical sketches Furthemore, I have significantly beefed up the subject index to help the reader na-vigate the book more easily.

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Abbreviations
Alder ene reaction
Aldol condensation
Algar-Flynn-Oyamade reaction
Allan-Robinson reaction
Appel reaction’
Arndt-Eistert homologation
Baeyer-Villiger oxidation
Baker-Venkataramen rearragement
Bamberger rearrangement
Bamford-Stevents reaction
Barbier coupling reaction
Bargellini reaction
Bartoli indole synthesis
Barton radical decarboxylation
Barton-McCombie deoxygenation
Barton nitrite photolysis
Barton-Zard reaction
Batcho-Leimgruber indole synthesis
Baylis-Hillman reaction
Beckmann rearrangement
Beirut reaction
Benzilic acid rearragement
Benzoin condensation
Bergman cycliztion
Biginelli pyrimidone synthesis
Birch reduction
Bischler-Mohlau indole synthesis
Bischler-Napieralski reaction
……
Zincke reaction
Subject Index
………

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