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Difunctionalization of Alkenes Involving Metal Migration

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 59, 期 21, 页码 7990-8003

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201913382

关键词

alkenes; regioselectivities; reaction mechanisms; synthetic methods; transition metals

资金

  1. National Natural Science Foundation of China [21702151, 21871211, 21801193]
  2. Fundamental Research Funds for Central Universities [2042019kf0208]

向作者/读者索取更多资源

The direct difunctionalization of alkenes, a cheap and abundant feedstock, represents one of the most attractive strategies for increasing molecular complexity in synthetic organic chemistry. In contrast with the 1,2-difunctionalization of alkenes, recent advances showcase alkene 1,n-difunctionalizations (n not equal 2) involving metal migration is an emerging and rapidly growing area of research. This promising strategy not only opens a novel avenue for future development of alkene transformations, but also significantly expands upon the bond disconnections available in modern organic synthesis. This Minireview summarizes recent progress in the migratory difunctionalization of alkenes, with an emphasis on the driving force for metal migration.

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