迈克尔反应

E. Bergmann, D. Ginsburg, R. Pappo
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引用次数: 27

摘要

迈克尔缩合的原始范围是将OCCH体系中含有α -氢原子的加体或供体加到碳-碳双键上,形成受体中通式CCCO共轭体系的一部分。缩合是在碱性试剂的作用下发生的,通常是碱金属醇氧化物。加数的范围很广。典型的受体是α, β -不饱和醛,酮和酸衍生物。作为原范围的延伸,迈克尔缩合反应已被理解为包括由羰基和羧基以外的基团激活的加体和受体。这一调查涵盖了更广泛的范围。关键词:迈克尔反应;副反应;加合物;桥接中间体;环丙烷衍生物;迈克尔凝结;酮;酯;环烷酮;环烯;罗宾逊的修改;芳香环系;环;吡咯;哌啶;pyrrolizidines;氨基酸盐;实验条件
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The Michael Reaction
The Michael condensation in its original scope is the addition of an addend or donor containing an alpha-hydrogen atom in the system OCCH to a carbon-carbon double bond that forms part of a conjugated system of the general formula CCCO in an acceptor. The condensation takes place under the influence of alkaline reagents, typically alkali metal alkoxides. The range of addends is very broad. Typical acceptors are alpha, beta-unsaturated aldehydes, keotnes, and acid derivatives. As an extension of the original scope, the Michael condensation has come to be understood to include addends and acceptors activated by groups other than carbonyl and carboxalkoxy. The wider scope is encompassed in this survey. Keywords: Michael reaction; side reaction; adduct; bridged intermediates; cyclopropane derivatives; Michael condensation; ketones; esters; cycloalkanones; cycloalkenes; Robinson's modification; aromatic rings systems; rings; pyrroles; piperidines; pyrrolizidines; amino salts; experimental conditions
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CiteScore
4.40
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