4.5 Review

Heck-Like Reactions Involving Heteroatomic Electrophiles

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2017, 期 34, 页码 4996-5009

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201700485

关键词

Heck reaction; Homogeneous catalysis; Synthetic methods; Palladium

资金

  1. University of Delaware
  2. National Science Foundation [CAREER CHE-1254360]
  3. National Institute of General Medical Science [P20GM104316]
  4. Delaware Economic Development Office [16A00384]
  5. Research Corporation Cottrell Scholars Program

向作者/读者索取更多资源

Since the discovery of the Heck reaction in the early seventies, the reaction has become a powerful tool in synthetic organic chemistry. By employing heteroatomic instead of traditional carbon electrophiles, the Heck reaction shows an intriguing flexibility. These hetereoatomic Heck reactions reinvigorate the area, by offering new routes to highly useful synthetic precursors and structural motifs present in biologically active compounds. This microreview focuses on early developments leading to the heteroatomic-Heck reactions (silyl-Heck, boryl-Heck and intramolecular aza-Heck), current state of the emerging area, as well as that of a few related processes.

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