The anti-selective boron-mediated asymmetric aldol reaction of carboxylic esters

被引：179

作者：

Abiko, A ^{[1
]}

Liu, JF ^{[1
]}

Masamune, S ^{[1
]}

机构：

[1] MIT,DEPT CHEM,CAMBRIDGE,MA 02139

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1997年 / 119卷 / 10期

关键词：

D O I：

10.1021/ja963754f

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

[No abstract available]

引用

页码：2586 / 2587

页数：2

共 33 条

[1] Concerning the boron-mediated aldol reaction of carboxylic esters [J].

Abiko, A ;

Liu, JF ;

Masamune, S .

JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (08) :2590-2591

[2] ANTI-SELECTIVE AND DIASTEREOFACIALLY SELECTIVE ALDOL REACTIONS WITH (R)-2-SILOXY-1,2,2-TRIPHENYLETHYL PROPIONATE [J].

BRAUN, M ;

SACHA, H .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1991, 30 (10) :1318-1320

[3] RECENT ADVANCES IN STEREOSELECTIVE ALDOL REACTIONS OF ESTER AND THIOESTER ENOLATES [J].

BRAUN, M ;

SACHA, H .

JOURNAL FUR PRAKTISCHE CHEMIE-CHEMIKER-ZEITUNG, 1993, 335 (08) :653-668

[4] THE E/Z GEOMETRY OF THE ENOLATE COMPONENT DETERMINES FACE SELECTION OF THE ALDEHYDE COMPONENT IN CHIRAL DIAZABOROLIDINE-DIRECTED ENANTIOSELECTIVE ALDOL COUPLING [J].

COREY, EJ ;

LEE, DH .

TETRAHEDRON LETTERS, 1993, 34 (11) :1737-1740

[5] ACYCLIC STEREOSELECTION .48. REVERSAL OF STEREOCHEMISTRY IN THE ALDOL REACTIONS OF A CHIRAL BORON ENOLATE [J].

DANDA, H ;

HANSEN, MM ;

HEATHCOCK, CH .

JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (01) :173-181

[6] CHIRAL PROPIONATE ENOLATE EQUIVALENTS FOR THE STEREOSELECTIVE SYNTHESIS OF THREO-ALPHA-METHYL-BETA-HYDROXY OR ERYTHRO-ALPHA-METHYL-BETA-HYDROXY ACIDS [J].

DAVIES, SG ;

DORDORHEDGECOCK, IM ;

WARNER, P .

TETRAHEDRON LETTERS, 1985, 26 (17) :2125-2128

[7] ENANTIOSELECTIVE SYNTHESES WITH TITANIUM-CARBOHYDRATE COMPLEXES .5. ENANTIOSELECTIVE AND DIASTEREOSELECTIVE ALDOL-REACTION OF 2,6-DIMETHYLPHENYL PROPIONATE USING TITANIUM-CARBOHYDRATE COMPLEXES [J].

DUTHALER, RO ;

HEROLD, P ;

WYLERHELFER, S ;

RIEDIKER, M .

HELVETICA CHIMICA ACTA, 1990, 73 (03) :659-673

[8]

Fleming I., 1991, Comprehensive Organic Synthesis, V2, P563

[9] THE RATIONAL DESIGN OF HIGHLY STEREOSELECTIVE BORON ENOLATES USING TRANSITION-STATE COMPUTER MODELING - A NOVEL, ASYMMETRIC ANTI-ALDOL REACTION FOR KETONES [J].

GENNARI, C ;

HEWKIN, CT ;

MOLINARI, F ;

BERNARDI, A ;

COMOTTI, A ;

GOODMAN, JM ;

PATERSON, I .

JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (19) :5173-5177

[10] COMPUTER-ASSISTED DESIGN OF CHIRAL BORON ENOLATES - A NOVEL, HIGHLY ENANTIOSELECTIVE ALDOL REACTION FOR THIOACETATES AND THIOPROPIONATES [J].

GENNARI, C ;

MORESCA, D ;

VIETH, S ;

VULPETTI, A .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1993, 32 (11) :1618-1621

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