Acyclic stereocontrol in radical reactions. Effect of precursor stereochemistry on selectivity in allylations.

被引：0

作者：

Sibi, MP ^{[1
]}

Ternes, TR ^{[1
]}

机构：

[1] N Dakota State Univ, Dept Chem, Fargo, ND 58105 USA

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1999年 / 217卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

384-ORGN

引用

页码：U179 / U179

页数：1

共 21 条

[1] Higher selectivity at higher temperatures! Effect of precursor stereochemistry on diastereoselectivity in radical allylations. Insight into the role of the Lewis acid
Sibi, MP
Rheault, TR
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (37) : 8873 - 8879
[2] Acyclic stereocontrol in radical reactions. Diastereoselective radical addition/allylation of N-propenoyloxazolidinone
Sibi, MP
Ji, JG
JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (18): : 6090 - 6091
[3] Acyclic stereocontrol in radical reactions: rho-selectivity with oxazolidinone auxiliaries
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Ji, JG
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1996, 35 (02): : 190 - 192
[4] New chiral auxiliary for asymmetric thermal reactions. High stereocontrol in radical addition, allylation, and annulation reactions
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Curran, Dennis P.
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Journal of the American Chemical Society, 1992, 114 (18):
[5] Stereochemistry of radical halogenation reactions. An ab initio molecular orbital study
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[6] A Computational Study on Lewis Acid-Catalyzed Diastereoselective Acyclic Radical Allylation Reactions with Unusual Selectivity Dependence on Temperature and Epimer Precursor
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JOURNAL OF ORGANIC CHEMISTRY, 2014, 79 (23): : 11483 - 11495
[7] ACYCLIC STEREOCONTROL OF FREE-RADICAL REACTIONS INVOLVING ALKYL 2-(1-HYDROXYALKYL)PROPENOATES
EASTWOOD, FW
MIFSUD, RD
PERLMUTTER, P
AUSTRALIAN JOURNAL OF CHEMISTRY, 1994, 47 (12) : 2187 - 2200
[8] Enantioselective tandem radical reactions: Vicinal difunctionalization in acyclic systems with control over relative and absolute stereochemistry
Sibi, MP
Chen, JX
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (38) : 9472 - 9473
[9] Geminal selectivity of singlet oxygen ene reactions. The nonbonding large group effect
1600, (112):
[10] Radical cation-nucleophile combination reactions. The effect of structure of nitrogen-centered nucleophiles on reaction rates
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Reitstoen, B
ACTA CHEMICA SCANDINAVICA, 1997, 51 (10): : 1035 - 1040

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