Highly (≥98%) Stereo- and Regioselective Trisubstituted Alkene Synthesis of Wide Applicability via 1-Halo-1-alkyne Hydro- boration-Tandem Negishi-Suzuki Coupling or Organoborate Migratory Insertion-Reference-Cited by-同舟云学术

Highly (≥98%) Stereo- and Regioselective Trisubstituted Alkene Synthesis of Wide Applicability via 1-Halo-1-alkyne Hydro- boration-Tandem Negishi-Suzuki Coupling or Organoborate Migratory Insertion

Published:2011-10-20 Issue:16 Volume:353 Page:2981-2987
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Xu Shiqing,Lee Ching-Tien,Rao Honghua,Negishi Ei-ichi

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/adsc.201100420/fullpdf

Reference51 articles.

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2. The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects

3. Phosphororganische Verbindungen, XX. Phosphinoxyde als Olefinierungsreagenzien

4. The Utility of Phosphonate Carbanions in Olefin Synthesis

5. Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.

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