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Design and Synthesis of Spirocycles

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2017, 期 36, 页码 5316-5342

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201700439

关键词

Spiro compounds; Olefin metathesis; Enyne metathesis; Cycloaddition; Claisen rearrangement; Grignard addition; Fischer indolization; Suzuki-Miyaura; Cross-coupling; Retro Diels-Alder (rDA) reaction

资金

  1. Department of Science and Technology (DST), New Delhi [EMR/2015/002053]
  2. DST [SR/S2/JCB-33/2010]
  3. Indian Institute of Technology (IIT)-Bombay

向作者/读者索取更多资源

In this account we disclose a variety of simple strategies demonstrated in our laboratory in the last two decades for the assembly of diverse and intricate molecular frameworks containing spiro linkage(s) by using various metathesis protocols such as ring-closing metathesis (RCM), ring-opening cross-metathesis (ROCM), ring-closing enyne metathesis (RCEM) and ring-rearrangement metathesis (RRM). Also, cycloaddition reactions ([2+2], [4+2] and [2+2+2]) and other key processes such as Claisen rearrangement (CR), Grignard addition, Fischer indolization (FI), Suzuki-Miyaura (SM) cross-coupling and the retro-Diels-Alder (rDA) reaction have been used as key steps to construct spirocycles.

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