Enantioselective Route to 5-Methyl- and 5,7-Dimethyl-6,7-dihydro-5H-dibenz[c,e]azepine: Secondary Amines with Switchable Axial Chirality-Reference-Cited by-同舟云学术

Enantioselective Route to 5-Methyl- and 5,7-Dimethyl-6,7-dihydro-5H-dibenz[c,e]azepine: Secondary Amines with Switchable Axial Chirality

Published:2009-03-10 Issue:7 Volume:11 Page:1663-1666
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Pira Silvain L.¹,Wallace Timothy W.¹,Graham Jonathan P.¹

Affiliation:

1. School of Chemistry, The University of Manchester, Oxford Road, Manchester M13 9PL, U.K., and GlaxoSmithKline, Medicines Research Centre, Gunnels Wood Road, Stevenage, Herts SG1 2NY, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol900333c

Reference65 articles.

1. BINAP: an efficient chiral element for asymmetric catalysis

2. Bioactive alkaloids. 4. Results of recent investigations with colchicine and physostigmine

3. bFor a correction, see:

4. The Absolute Configuration of Colchicine by Correct Application of theCIP Rules

5. aS,7S-absolute configuration of natural (−)-colchicine and allocongeners

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