Wagner–Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols: vinyl migration in preference to aryl migration-Reference-Cited by-同舟云学术

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Wagner–Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols: vinyl migration in preference to aryl migration

Published:2014-11 Issue:44 Volume:70 Page:8374-8379
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Fu Jian-Guo,Ding Rui,Sun Bing-Feng,Lin Guo-Qiang

Funder

National Natural Science Foundation of China

National Basic Research Program of China

State Key Laboratory of Bioorganic and Natural Products Chemistry

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. For reviews on Wagner–Meerwein rearrangement, see:

2. Electronegatively substituted carbocations

3. Recent studies of carbocations

4. 14-Step Synthesis of (+)-Ingenol from (+)-3-Carene

5. Synthese von 9-Fluorenalkanaminen, 2. Mitt. Versuche zur Cyclisierung von 4,4-disubstituierten Diphenylaminoalkoholen zu 3,6-disubstituierten 2-(9H-Fluoren-9-yl)-2-propanaminen

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1. Wagner–Meerwein Rearrangement;Name Reactions;2021

2. [1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides;Beilstein Journal of Organic Chemistry;2020-01-21

3. Carbocations;Organic Reaction Mechanisms · 2014;2018-01-05

4. Molecular Rearrangements;Organic Reaction Mechanisms · 2014;2018-01-05

5. ChemInform Abstract: Wagner-Meerwein Rearrangement of [3.3.1] Bicyclic N-Boc Aminols: Vinyl Migration in Preference to Aryl Migration.;ChemInform;2015-03-19

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