ChemInform Abstract: Highly Selective Ylide-Initiated Michael Addition/Cyclization Reaction for Synthesis of Cyclohexadiene Epoxide and Vinylcyclopropane Derivatives

Treatment of α,β‐unsaturated ketones with the sulfonium salt (I) and the weak base Cs2CO3 results in efficient and stereoselective formation of cyclohexadiene epoxides like (III).

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Veröffentlicht in:ChemInform 2010-09, Vol.41 (38), p.no-no
Hauptverfasser: Zhu, Ben-Hu, Zhou, Rui, Zheng, Jun-Cheng, Deng, Xian-Ming, Sun, Xiu-Li, Shen, Qi, Tang, Yong
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container_end_page no
container_issue 38
container_start_page no
container_title ChemInform
container_volume 41
creator Zhu, Ben-Hu
Zhou, Rui
Zheng, Jun-Cheng
Deng, Xian-Ming
Sun, Xiu-Li
Shen, Qi
Tang, Yong
description Treatment of α,β‐unsaturated ketones with the sulfonium salt (I) and the weak base Cs2CO3 results in efficient and stereoselective formation of cyclohexadiene epoxides like (III).
doi_str_mv 10.1002/chin.201038103
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source Wiley Online Library Journals Frontfile Complete
subjects cyclopropane derivatives
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
oxirane derivatives
polyphenyl derivatives
title ChemInform Abstract: Highly Selective Ylide-Initiated Michael Addition/Cyclization Reaction for Synthesis of Cyclohexadiene Epoxide and Vinylcyclopropane Derivatives
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