γ′-Selective Functionalization of Cyclic Enones: Construction of a Chiral Quaternary Carbon Center by [4+2] Cycloaddition/Retro-Mannich Reaction with 3-Substituted Maleimides-Reference-Cited by-同舟云学术

γ′-Selective Functionalization of Cyclic Enones: Construction of a Chiral Quaternary Carbon Center by [4+2] Cycloaddition/Retro-Mannich Reaction with 3-Substituted Maleimides

Published:2016-10-13 Issue:46 Volume:128 Page:14469-14473
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Zou Chuncheng¹,Zeng Chuikun¹,Liu Zhen²,Lu Min¹,Sun Xiaohua¹,Ye Jinxing¹

Affiliation:

1. Engineering Research Centre of Pharmaceutical Process Chemistry; Ministry of Education; Shanghai Key Laboratory of New Drug Design; School of Pharmacy; East China University of Science and Technology; 130 Meilong Road Shanghai 200237 China

2. State Key Laboratory of Chemical Engineering; East China University of Science and Technology; Shanghai 200237 China

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201605790/fullpdf

Reference95 articles.

1. Photoinduced molecular transformations. Part 150. A new total synthesis of (±)-α-Himachalene based on a Sequence involving [2+2] photoaddition and regioselective β-scission of alkoxyl radicals generated from the resulting cyclobutanols

2. Improved Synthesis of Cyclic Tertiary Allylic Alcohols by Asymmetric 1,2-Addition of AlMe3to Enones

3. Enantioselective palladium catalyzed conjugate additions of ortho-substituted arylboronic acids to β,β-disubstituted cyclic enones: total synthesis of herbertenediol, enokipodin A and enokipodin B

4. Catalytic Enantioselective Construction of Quaternary Stereocenters: Assembly of Key Building Blocks for the Synthesis of Biologically Active Molecules

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