Convergent synthesis of conjugated 1,2-disubstituted E-allylic alcohols from two aldehydes and methylenetriphenylphosphorane
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2012/OB/C2OB26346G
Reference27 articles.
1. Modification of the Wittig reaction to permit the stereospecific synthesis of certain trisubstituted olefins. Stereospecific synthesis of .alpha.-santalol
2. On the origin of stereo- and position selectivity in the synthesis of allylic alcohols from β-oxido ylides
3. Stereochemistry and Mechanism in the Wittig Reaction
4. SCOOPY-Reaktionen: Stereoselektivität der Allyl-alkohol-Synthese via Betain-Ylide
5. SCOOPY-Reaktionen: Die Regioselektivität der Alkenol-Synthese
Cited by 2 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. ChemInform Abstract: Convergent Synthesis of Conjugated 1,2-Disubstituted E-Allylic Alcohols from Two Aldehydes and Methylenetriphenylphosphorane.;ChemInform;2013-03-08
2. Alkenes from β-lithiooxyphosphonium ylides generated by trapping α-lithiated terminal epoxides with triphenylphosphine;Beilstein Journal of Organic Chemistry;2012-11-07
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