A facile stereoselective synthesis of 1,4-dienyl sulfides via Stille coupling reactions of (E)-α-stannylvinyl sulfides with allylic bromides
Author:
Affiliation:
1. Department of Chemistry, Jiangxi Normal University, Nanchang 330022, China
Abstract
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/030823406780199749
Reference14 articles.
1. Construction of (Z,Z ) skipped 1,4-dienes. Application to the synthesis of polyunsaturated fatty acids and derivatives †
2. The Baylis−Hillman Reaction: One-Pot Facile Synthesis of 2,4-Functionalized 1,4-Pentadienes
3. One-Pot Synthesis of a Variety of 1,4-Alkadienes and 1,2,4-Alkatrienes from Alkynes, Allyl, or Propargyl Compounds and Electrophiles by a (η2-Propene)Ti(O-i-Pr)2-Mediated Reaction
4. New route to biologically active 3,8-dioxabicyclo[3.2.1]octane derivatives related to zoapatanol
5. Alkylation-reduction of carbonyl systems. 10. Regiospecific synthesis of 1,4-dienes by alkylation-reduction of .alpha.,.beta.,.gamma.,.delta.-unsaturated ketones
Cited by 3 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. 3.03 Alkylation of α-Sulfur-Containing Carbanions;Comprehensive Organic Synthesis II;2014
2. Stille Coupling;Comprehensive Organic Name Reactions and Reagents;2010-09-15
3. A Facile Stereoselective Synthesis of 1,4-Dienyl Sulfides via Stille Coupling Reactions of (E)-α-Stannylvinyl Sulfides with Allylic Bromides.;ChemInform;2007-05-22
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