One-Pot Synthesis ofO-Allylhydroxylamines through the Organocatalytic Oxidation of Tertiary Allylic Amines Followed by a [2,3]-Meisenheimer Rearrangement-Reference-Cited by-同舟云学术

One-Pot Synthesis ofO-Allylhydroxylamines through the Organocatalytic Oxidation of Tertiary Allylic Amines Followed by a [2,3]-Meisenheimer Rearrangement

Published:2015-02-12 Issue:13 Volume:21 Page:5238-5241
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Theodorou Alexis,Limnios Dimitris,Kokotos Christoforos G.

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference38 articles.

1. Über eine eigenartige Umlagerung des Methyl‐allyl‐anilin‐ N ‐oxyds

2. Asymmetric synthesis of (R)-hexane-1,5-diol, (R)-hex-3-ene-1,5-diol and (R)-6-methylhept-5-en-2-ol (sulcatol) employing a tandem asymmetric conjugate addition and stereospecific Meisenheimer rearrangement protocol

3. Chirality Transfer from Nitrogen to Carbon in the [2,3]-Meisenheimer Rearrangement

4. Studies on the [2,3]-Meisenheimer Rearrangement of 2-Vinylazetidine N-Oxides.

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