有機合成化学協会誌
Online ISSN : 1883-6526
Print ISSN : 0037-9980
ISSN-L : 0037-9980
総説および総合論文
立体化学的に不安定なキラルカルバニオンの合成化学への展開
佐々木 道子武田 敬
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2013 年 71 巻 2 号 p. 136-148

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This account presents our recent efforts in exploring the synthetic potential of configurationally labile chiral carbanions next to electron-withdrawing groups that have been considered to be impossible even to generate. We used epoxysilane rearrangement to generate a chiral carbanion whose chirality was transformed from epoxide. The detailed analysis of the process showed that a carbamoyloxy group plays a more prominent role in fixing a chiral lithiocarbanion than expected. This understanding has led to the successful development of a method that allows enantioselective trapping of an α-chiral carbanion of acyclic nitrile by a carbon electrophile. During the course of these studies, we have found that the configurational stability of a carbanion highly depends on the solvent and we have proposed that the dependency is attributable to the ratio of CIP and SIP associated with their solvated structures.

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© 2013 社団法人 有機合成化学協会
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