Efficient Synthesis of the 3-Benzazepine Framework via Intramolecular Heck Reductive Cyclization-Reference-Cited by-同舟云学术

Efficient Synthesis of the 3-Benzazepine Framework via Intramolecular Heck Reductive Cyclization

Published:2007-07-03 Issue:16 Volume:9 Page:3017-3020
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Donets Pavel A.¹,Van der Eycken Erik V.¹

Affiliation:

1. Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol071079g

Reference27 articles.

1. Cyclic sulfamidates as lactam precursors. An efficient asymmetric synthesis of (-)-aphanorphine

2. A Facile Asymmetric Route to (−)-Aphanorphine

3. Total Synthesis of (±)-Lennoxamine and (±)-Aphanorphine by Intramolecular Electrophilic Aromatic Substitution Reactions of 2-Amidoacroleins

4. Cyclic sulfamidates as versatile lactam precursors. An evaluation of synthetic strategies towards (−)-aphanorphine

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