STEREOSELECTIVE ALDOL REACTIONS VIA TITANIUM ENOLATES

被引：27

作者：

MURPHY, PJ ^{[1
]}

PROCTER, G ^{[1
]}

RUSSELL, AT ^{[1
]}

机构：

[1] UNIV SALFORD,DEPT CHEM & APPL CHEM,SALFORD M5 4WT,LANCS,ENGLAND

来源：

TETRAHEDRON LETTERS | 1987年 / 28卷 / 18期

关键词：

D O I：

10.1016/S0040-4039(00)96039-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：2037 / 2040

页数：4

共 8 条

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[2]

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[3]

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[4] ORGANOBORON COMPOUNDS IN ORGANIC-SYNTHESIS .4. ASYMMETRIC ALDOL REACTIONS [J].

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SATO, T ;

KIM, BM ;

WOLLMANN, TA .

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[5] APPARENT CHELATION CONTROL IN ALDOL REACTIONS OF CHIRAL (ME2CHO)3TI-ENOLATES [J].

NERZSTORMES, M ;

THORNTON, ER .

TETRAHEDRON LETTERS, 1986, 27 (08) :897-900

[6] IMPROVED ENANTIOSELECTIVE SYNTHESIS OF ANTI ALPHA-METHYL-BETA-HYDROXYESTERS THROUGH TICL4-PPH3 MEDIATED ALDOL CONDENSATION [J].

PALAZZI, C ;

COLOMBO, L ;

GENNARI, C .

TETRAHEDRON LETTERS, 1986, 27 (15) :1735-1738

[7]

REETZ MT, 1981, TETRAHEDRON LETT, V22, P4619

[8] VERY HIGH DIASTEREOFACIAL SELECTIVITIES IN CONVENIENT TITANIUM-MEDIATED ALDOL REACTIONS [J].

SIEGEL, C ;

THORNTON, ER .

TETRAHEDRON LETTERS, 1986, 27 (04) :457-460

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