STEREOSELECTIVE BROMINATION OF ALLYLIC ALCOHOLS - A FACILE SYNTHESIS OF E-BROMOEPOXIDES OR Z-BROMOEPOXIDES FROM A COMMON STARTING MATERIAL

被引：0

作者：

MIDLAND, MM ^{[1
]}

HALTERMAN, RL ^{[1
]}

机构：

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

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1980年 / 180卷 / AUG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：197 / ORGN

共 17 条

[11] PIPERONAL AS STARTING MATERIAL FOR THE REGIOSPECIFIC AND STEREOSELECTIVE SYNTHESIS OF E-ISOMERS AND Z-ISOMERS OF 3-METHYL-2-HEXENEDIOIC ACID-1-METHYL ESTER
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[12] Stereoselective synthesis of (E,Z)-3,4-dialkylidene-N-phenylpyrrolidine-2,5-diones starting from Morita-Baylis-Hillman carbonates
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[13] A facile stereoselective synthesis of (Z)-2-ethoxycarbonyl-substituted 1,3-enynes from (E)-α-stannyl-α,β-unsaturated esters and alkynyl bromides
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[14] Mild and practical stereoselective synthesis of (Z)- and (E)-allyl bromides from Baylis-Hillman adducts using Appel agents (PPh3/CBr4): a facile synthesis of semiplenamides C and E
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[15] An expedient stereoselective synthesis of (Z)- and (E)-ally iodides from Baylis-Hillman adducts along with selective iodination of benzylic alcohols using the polymethylhydrosiloxane-iodine system
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[16] REACTION OF COPPER ENOLATES OF ESTERS WITH PROPARGYLIC SYSTEMS - FACILE PREPARATION OF 3,4-DIENOIC ESTERS, STEREOSELECTIVE REARRANGEMENT TO (2E,4Z)-DIENOIC AND (2E,4E)-DIENOIC ESTERS, AND STEREOSELECTIVE SYNTHESIS OF A FRAGRANCE FROM BARTLETT PEAR
AMOS, RA
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JOURNAL OF ORGANIC CHEMISTRY, 1978, 43 (04): : 555 - 560
[17] Stereoselective Synthesis of (2Z,4E)-2,4-Pentadien-1-ols via Sequential 1,4-Elimination Reaction and [1,2]-Wittig Rearrangement Starting from (E)-4-Alkoxy-2-butenyl Benzoates
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