ASYMMETRIC REDUCTION OF ALPHA-ACETYLENIC, BETA-ACETYLENIC KETONES IN HIGH ENANTIOMERIC EXCESS WITH B-3-PINANYL-9-BORABICYCLO[3.3.1]NONANE

被引：0

作者：

MIDLAND, MM ^{[1
]}

MCDOWELL, DC ^{[1
]}

TRAMONTANO, A ^{[1
]}

机构：

[1] UNIV CALIF RIVERSIDE,DEPT CHEM,RIVERSIDE,CA 92521

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1979年 / APR期

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：449 / 449

页数：1

共 25 条

[21] REMARKABLE OPTICAL INDUCTION IN THE REDUCTION OF ALPHA-KETO ESTERS WITH B-(3-PINANYL)-9-BORABICYCLO[3.3.1]NONANE - SYNTHESIS OF ALPHA-HYDROXY ESTERS OF 100-PERCENT OPTICAL PURITY
BROWN, HC
PAI, GG
JADHAV, PK
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (05) : 1531 - 1533
[22] Hydroboration. 94. Rates of Hydroboration of 2-Organylapopinenes with 9-Borabicyclo[3.3.1]nonane, Providing B-(2-Organylapoisopinocampheyl)-9-borabicyclo[ @3.3.1] nonanes, Potentially Valuable for the Asymmetric Reduction of Prochiral Ketones
Dhokte, U. P.
Brown, H. C.
Journal of Organic Chemistry, 62 (04):
[23] SELECTIVE REDUCTIONS .53. ASYMMETRIC REDUCTION OF ALPHA-FLUOROMETHYL KETONES WITH B-CHLORODIISOPINOCAMPHEYLBORANE AND B-ISOPINOCAMPHEYL-BORABICYCLO[3.3.1]NONANE - COMBINED ELECTRONIC AND STERIC CONTRIBUTIONS TO THE ENANTIOCONTROL PROCESS
RAMACHANDRAN, PV
TEODOROVIC, AV
GONG, BQ
BROWN, HC
TETRAHEDRON-ASYMMETRY, 1994, 5 (06) : 1075 - 1086
[24] SELECTIVE REDUCTIONS .22. FACILE REDUCTION OF ALPHA, BETA-UNSATURATED ALDEHYDES AND KETONES WITH 9-BORABICYCLO[3.3.1]NONANE - REMARKABLY CONVENIENT PROCEDURE FOR SELECTIVE CONVERSION OF CONJUGATED ALDEHYDES AND KETONES TO CORRESPONDING ALLYLIC ALCOHOLS IN PRESENCE OF OTHER FUNCTIONAL-GROUPS
KRISHNAMURTHY, S
BROWN, HC
JOURNAL OF ORGANIC CHEMISTRY, 1977, 42 (07): : 1197 - 1201
[25] STEREOCONTROLLED SYNTHESIS OF 22-HYDROXY-23-ACETYLENIC STEROIDS, KEY INTERMEDIATES IN STEROID SIDE-CHAIN CONSTRUCTION - OBSERVATION OF A DIRECTIVE EFFECT BY AN ALPHA-CHIRAL SITE DURING ASYMMETRIC REDUCTION WITH B-3-PINANYL-9-BBN (ALPINE-BORANE)
MIDLAND, MM
KWON, YC
TETRAHEDRON LETTERS, 1984, 25 (52) : 5981 - 5984

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