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 31 条

[1] Ene reaction of singlet oxygen, triazolinedione, and nitrosoarene with chiral deuterium-labeled allylic alcohols: The interdependence of diastereoselectivity and regioselectivity discloses mechanistic insights into the hydroxy-group directivity
Adam, W
Bottke, N
Krebs, O
Lykakis, I
Orfanopoulos, M
Stratakis, M
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (48) : 14403 - 14409
[2] HYDROXY-DIRECTED REGIOSELECTIVE AND DIASTEREOSELECTIVE ENE REACTION OF SINGLET OXYGEN WITH CHIRAL ALLYLIC ALCOHOLS
ADAM, W
NESTLER, B
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (12) : 5041 - 5049
[3] PHOTOOXYGENATION OF CHIRAL ALLYLIC ALCOHOLS - HYDROXY-DIRECTED REGIOSELECTIVE AND DIASTEREOSELECTIVE ENE REACTION OF SINGLET OXYGEN
ADAM, W
NESTLER, B
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (16) : 6549 - 6550
[4] Regio- and diastereoselective catalytic epoxidation of chiral allylic alcohols with hexafluoroacetone perhydrate.: Hydroxy-group directivity through hydrogen bonding
Adam, W
Degen, HG
Saha-Möller, CR
JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (04): : 1274 - 1277
[5] Regio- and diastereoselective catalytic epoxidation of chiral allylic alcohols with hexafluoroacetone perhydrate. Hydroxy-group directivity through hydrogen bonding
J Org Chem, 4 (1274-1277):
[6] Hydroxy-directed diastereoselective ene reaction of triazolinediones with chiral allylic alcohols
Adam, W
Nestler, B
Pastor, A
Wirth, T
TETRAHEDRON LETTERS, 1998, 39 (17) : 2625 - 2628
[7] Hydroxy group directivity in the epoxidation of chiral allylic alcohols: Control of diastereoselectivity through allylic strain and hydrogen bonding
Adam, W
Wirth, T
ACCOUNTS OF CHEMICAL RESEARCH, 1999, 32 (08) : 703 - 710
[8] The nitroso ene reaction: A regioselective and stereoselective allylic nitrogen functionalization of mechanistic delight and synthetic potential
Adam, W
Krebs, O
CHEMICAL REVIEWS, 2003, 103 (10) : 4131 - 4146
[9] Photooxygenation of chiral allylic alcohols. Hydroxy-directed regio- and diastereoselective ene reaction of singlet oxygen
1600, (114):
[10] Hydroxy-group directivity in the regioselective and diastereoselective [2+2] photocycloaddition (Paternò-Büchi reaction) of aromatic carbonyl compounds to chiral and achiral allylic substrates: The preparation of oxetanes with up to three stereogenic centers as synthetic building blocks
Adam, W.
Stegmann, V.R.
Synthesis, 2001, (08) : 1203 - 1214

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