Secondary Products from Intramolecular Cycloadditions of Azidoalkyl Enol Ethers and Azidoalkyl Vinyl Bromides: 1-Azadienes, Their Reactions with Diphenylketene, and Radical Cyclizations To Form Bi- and Tricyclic Lactams
Author:
Affiliation:
1. Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford OX1 3TA, U.K.
2. Eli Lilly and Company Limited, Erl Wood Manor, Windlesham, Surrey GU20 6PH, U.K.
Funder
Engineering and Physical Sciences Research Council
Eli Lilly and Company
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b02005
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2. Access to a Guanacastepene and Cortistatin-Related Skeleton via Ethynyl Lactone Ireland–Claisen Rearrangement and Transannular (4 + 3)-Cycloaddition of an Azatrimethylenemethane Diyl
3. 1.3‐Dipolare Cycloadditionen, XIV: Die Anlagerung organischer Azide an Enoläther: Orientierung und Triazolin‐Zerfall
4. 1.3‐Dipolare Cycloadditionen, XV: Der sterische Ablauf der Azid‐Addition an Enoläther
5. Enoläther, XII1) Reaktionen von Cyclopropylolefinen und Enoläthern mit organischen Aziden
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