Synthesis of Multisubstituted Olefins through Regio- and Stereoselective Addition of Interelement Compounds Having B-Si, B-B, and Cl-S Bonds to Alkynes, and Subsequent Cross-Couplings-Reference-Cited by-同舟云学术

Synthesis of Multisubstituted Olefins through Regio- and Stereoselective Addition of Interelement Compounds Having B-Si, B-B, and Cl-S Bonds to Alkynes, and Subsequent Cross-Couplings

Published:2016-06-22 Issue:4 Volume:16 Page:2031-2045
ISSN:1527-8999
Container-title:The Chemical Record
language:en
Short-container-title:The Chemical Record

Author:

Iwasaki Masayuki¹,Nishihara Yasushi¹

Affiliation:

1. Research Institute for Interdisciplinary Science; 3-1-1 Tsushimanaka Kita-ku Okayama 700-8530 Japan

Publisher

Wiley

Subject

Materials Chemistry,General Chemical Engineering,Biochemistry,General Chemistry

Reference123 articles.

1. A highly efficient chemo- , regio- , and stereoselective synthesis of (7, 9)-dodecadien-1-yl acetate, a sex pheromone of , via a functionalized organoborate

2. Stereocontrolled Synthesis of Tetrasubstituted Olefins

3. Recent Advances in Efficient and Selective Synthesis of Di-, Tri-, and Tetrasubstituted Alkenes via Pd-Catalyzed Alkenylation−Carbonyl Olefination Synergy

4. Carbolithiation of Diphenylacetylene as a Stereoselective Route to (Z)-Tamoxifen and Related Tetrasubstituted Olefins

5. Novel Columnar Tetraphenylethenes via McMurry Coupling

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