A synthesis of allylsilanes in which the silyl group is at the more-substituted end of the allyl group
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1984/P1/P19840001809
Cited by 57 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Asymmetric Conjugate Addition of Grignard Reagents to 3-Silyl Unsaturated Esters for the Facile Preparation of Enantioenriched β-Silylcarbonyl Compounds and Allylic Silanes;Chemistry - A European Journal;2014-10-16
2. Preparation of (Ra)-Methyl 3-(dimethyl(phenyl)silyl)hexa-3,4-dienoatea;Organic Syntheses;2014-02-24
3. 2.02 Allylsilanes, Allylstannanes, and Related Compounds;Comprehensive Organic Synthesis II;2014
4. Reprint of: Enantiodivergent hydroboration reactions of a racemic allenylsilane with diisopinocampheylborane and Curtin–Hammett controlled double asymmetric crotylboration reactions of (S)-E-α-phenyldimethylsilyl(ddiisopinocampheyl)-crotylborane;Tetrahedron;2013-09
5. Enantiodivergent hydroboration reactions of a racemic allenylsilane with diisopinocampheylborane and Curtin–Hammett controlled double asymmetric crotylboration reactions of (S)-E-α-phenyldimethylsilyl(ddiisopinocampheyl)-crotylborane;Tetrahedron;2013-07
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