Scope of enantioselective palladium(II)-catalyzed aerobic alcohol oxidations with (-)-sparteine

被引:78
作者
Mandal, SK [1 ]
Jensen, DR [1 ]
Pugsley, JS [1 ]
Sigman, MS [1 ]
机构
[1] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
关键词
D O I
10.1021/jo0269161
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Evaluation of the substrate scope for Pd(II)/(-)-sparteine catalyzed aerobic oxidative kinetic resolution of secondary alcohols is disclosed. An improved system is found with use of tert-butyl alcohol solvent in which benzylic and aliphatic alcohols as well as alcohols containing olefins are effectively oxidatively resolved. For substrates that successfully undergo oxidative kinetic resolution, k(rel) values are generally between 10 and 20. Successful scale-up of various substrates to 10-mmol scale is described. Extension to oxidative desymmetrization of 1,3-meso-diols is successful with enantiomeric excesses ranging from 78 to 85%.
引用
收藏
页码:4600 / 4603
页数:4
相关论文
共 60 条
[1]   Pd-catalyzed kinetic resolution of benzylic alcohols:: a practical synthesis of (R)-tomoxetine and (S)-fluoxetine hydrochlorides [J].
Ali, IS ;
Sudalai, A .
TETRAHEDRON LETTERS, 2002, 43 (31) :5435-5436
[2]   Palladium-catalyzed enantioselective oxidation of alcohols:: A dramatic rate acceleration by Cs2CO3/t-BuOH [J].
Bagdanoff, JT ;
Ferreira, EM ;
Stoltz, BM .
ORGANIC LETTERS, 2003, 5 (06) :835-837
[3]   The kinetic resolution of allylic alcohols by a non-enzymatic acylation catalyst; application to natural product synthesis [J].
Bellemin-Laponnaz, S ;
Tweddell, J ;
Ruble, JC ;
Breitling, FM ;
Fu, GC .
CHEMICAL COMMUNICATIONS, 2000, (12) :1009-1010
[4]   HOMOGENEOUS CATALYTIC-OXIDATION OF SECONDARY ALCOHOLS TO KETONES BY MOLECULAR-OXYGEN UNDER MILD CONDITIONS [J].
BLACKBURN, TF ;
SCHWARTZ, J .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1977, (05) :157-158
[5]   BIOCATALYTIC RESOLUTIONS OF ALPHA-METHYLENE-BETA-HYDROXY ESTERS AND KETONES [J].
BURGESS, K ;
JENNINGS, LD .
JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (04) :1138-1139
[6]   OPTICALLY-ACTIVE BUILDING-BLOCKS FROM THE SPAC REACTION - A COMPLETELY ASYMMETRIC-SYNTHESIS OF (4S-CIS)-5-(CYCLOHEXYLMETHYL)-4-HYDROXY-2-PYRROLIDINONE, A STATINE ANALOG [J].
BURGESS, K ;
CASSIDY, J ;
HENDERSON, I .
JOURNAL OF ORGANIC CHEMISTRY, 1991, 56 (06) :2050-2058
[7]   ENANTIOSELECTIVE ESTERIFICATIONS OF UNSATURATED ALCOHOLS MEDIATED BY A LIPASE PREPARED FROM PSEUDOMONAS SP [J].
BURGESS, K ;
JENNINGS, LD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (16) :6129-6139
[8]  
CARREIRA EM, 1999, COMPREHENSIVE ASYMME, V3, P997
[9]   Chiral Mitsunobu reactions with (1S)-(+)-ketopinic acid:: kinetic resolutions of secondary alcohols [J].
Chandrasekhar, S ;
Kulkarni, G .
TETRAHEDRON-ASYMMETRY, 2002, 13 (06) :615-619
[10]   Selection of enantioselective acyl transfer catalysts from a pooled peptide library through a fluorescence-based activity assay: An approach to kinetic resolution of secondary alcohols of broad structural scope [J].
Copeland, GT ;
Miller, SJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (27) :6496-6502