Catalytic Enantioselective β-Alkylation of α,β-Unsaturated Aldehydes by Combination of Transition-Metal- and Aminocatalysis: Total Synthesis of Bisabolane Sesquiterpenes

被引:63
作者
Afewerki, Samson [1 ]
Breistein, Palle [1 ]
Pirttila, Kristian [1 ]
Deiana, Luca [2 ,3 ]
Dziedzic, Pawel [2 ,3 ]
Ibrahem, Ismail [1 ]
Cordova, Armando [1 ,2 ,3 ]
机构
[1] Mid Sweden Univ, Dept Nat Sci Engn & Math, S-85170 Sundsvall, Sweden
[2] Univ Stockholm, Arrhenius Lab, Dept Organ Chem, S-10691 Stockholm, Sweden
[3] Stockholm Univ, Berzelii Ctr EXSELENT, S-10691 Stockholm, Sweden
关键词
aldehydes; alkylation; asymmetric conjugate additions; enantioselectivity; co-catalysis; zinc; ASYMMETRIC CONJUGATE ADDITION; PHASE-TRANSFER CATALYST; ALLYLIC ALKYLATION; ORGANOZINC COMPOUNDS; CASCADE CATALYSIS; BORONIC ESTERS; ZINC REAGENTS; COPPER; ACID; ORGANOCATALYSIS;
D O I
10.1002/chem.201100756
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Branching out! The first co-catalytic enantioselective (up to 98:2 e.r.) β-alkylation of α,β-unsaturated aldehydes by combination of simple chiral amine and copper catalysts provides β-branched aldehydes in a one-pot protocol (see scheme). The methodology was applied to the short total syntheses of bisabolane sesquiterpenes (S)-(+)-curcumene, (E)-(S)-(+)-3- dehydrocurcumene and (S)-(+)-tumerone. © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:8784 / 8788
页数:5
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