Hydroxy-group directivity in the nitroso ene reaction: Diastereo- and regioselective amination of chiral allylic alcohols

被引：22

作者：

Adam, W ^{[1
]}

Bottke, N ^{[1
]}

机构：

[1] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2000年 / 122卷 / 40期

关键词：

D O I：

10.1021/ja001752w

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：9846 / 9847

页数：2

共 13 条

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[2] HYDROXY-DIRECTED REGIOSELECTIVE AND DIASTEREOSELECTIVE ENE REACTION OF SINGLET OXYGEN WITH CHIRAL ALLYLIC ALCOHOLS
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[3] The new skew and the established cis and gem regioselectivities in the ene reaction of trisubstituted olefins:: Comparison of the singlet oxygen, triazolinedione, and nitrosoarene enophiles
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Krebs, O
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (28) : 6791 - 6792
[4] Hydroxy-directed diastereoselective ene reaction of triazolinediones with chiral allylic alcohols
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[J]. TETRAHEDRON LETTERS, 1998, 39 (17) : 2625 - 2628
[5] Diastereoselective singlet oxygen ene reaction (Schenck reaction) and diastereoselective epoxidations of heteroatom-substituted acyclic chiral olefins: A mechanistic comparison
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Kumar, AS
Peters, EM
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (08) : 1899 - 1905
[6] Hydroxy group directivity in the epoxidation of chiral allylic alcohols: Control of diastereoselectivity through allylic strain and hydrogen bonding
Adam, W
Wirth, T
[J]. ACCOUNTS OF CHEMICAL RESEARCH, 1999, 32 (08) : 703 - 710
[7] BRUNKER HG, 1995, J AM CHEM SOC, V117, P3976
[8] Regio- and diastereoselective ene reaction of 4-phenyl-1,2,4-triazoline-3,5-dione with chiral allylic alcohols and their derivatives
Gau, AH
Lin, GL
Uang, BJ
Liao, FL
Wang, SL
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (07) : 2194 - 2201
[9] GREENE FD, 1983, STEREOCHEMISTRY REAC, P197
[10] RATIONALIZATION OF NITROSOARENE-OLEFIN REACTIONS
KNIGHT, GT
PEPPER, B
[J]. TETRAHEDRON, 1971, 27 (24) : 6201 - &

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