Stereoselective formation of quaternary carbon centers and related functions

被引：492
作者：
Denissova, I [1 ]
Barriault, L [1 ]
机构：
[1] Univ Ottawa, Dept Chem, Ottawa, ON K1N 6N5, Canada
来源：
TETRAHEDRON | 2003年 / 59卷 / 51期
关键词：
quaternary carbon centers; enantioselective catalytic methods; electrophile;
D O I：
10.1016/j.tet.2003.10.039
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
[No abstract available]
引用
收藏
页码：10105 / 10146
页数：42
相关论文
共 173 条
[1]  
Aeilts SL, 2001, ANGEW CHEM INT EDIT, V40, P1452, DOI 10.1002/1521-3773(20010417)40:8<1452::AID-ANIE1452>3.0.CO
[2]  
2-G
[3]   Asymmetric arylation of ketone enolates [J].
Ahman, J ;
Wolfe, JP ;
Troutman, MV ;
Palucki, M ;
Buchwald, SL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (08) :1918-1919
[4]   Catalytic enantioselective ring-closing metathesis by a chiral biphen-Mo complex [J].
Alexander, JB ;
La, DS ;
Cefalo, DR ;
Hoveyda, AH ;
Schrock, RR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (16) :4041-4042
[5]   Enantioselective reformatsky reaction induced by chiral beta-amino alcohols [J].
Andres, JM ;
Martin, Y ;
Pedrosa, R ;
PerezEncabo, A .
TETRAHEDRON, 1997, 53 (10) :3787-3794
[6]   Synthesis of chiral, non-racemic aldols from chiral β-hydroxy-Weinreb amides prepared by enantioselective Reformatsky-like reaction induced by chiral β-aminoalcohols [J].
Andrés, JM ;
Pedrosa, R ;
Pérez-Encabo, A .
TETRAHEDRON, 2000, 56 (09) :1217-1223
[7]  
Angell RM, 1997, CHEM COMMUN, P919
[8]   Highly diastereoselective synthesis of decalin skeletons with quaternary carbon centers via the tandem oxy-cope/ene/Claisen reaction [J].
Barriault, L ;
Denissova, I .
ORGANIC LETTERS, 2002, 4 (08) :1371-1374
[9]   A new ligand class for the asymmetric dihydroxylation of olefins [J].
Becker, H ;
Sharpless, KB .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1996, 35 (04) :448-451
[10]  
BOECKMAN R, 1994, TETRAHEDRON LETT, V35, P3509
12345678910