Flexibility in the Partial Reduction of 2,5-Disubstituted Pyrroles: Application to the Synthesis of DMDP-Reference-Cited by-同舟云学术

Flexibility in the Partial Reduction of 2,5-Disubstituted Pyrroles: Application to the Synthesis of DMDP

Published:2003-03-08 Issue:7 Volume:5 Page:999-1002
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Donohoe Timothy J.¹,Headley Catherine E.¹,Cousins Rick P. C.¹,Cowley Andrew¹

Affiliation:

1. Dyson Perrins Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QY, United Kingdom, Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, United Kingdom, GlaxoSmithKline, Medicines Research Centre, Gunnels Wood Road, Stevenage, SG1 2NY, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol027504h

Reference11 articles.

1. Synthesis of Polyhydroxylated Pyrrolizidine Alkaloids of the Alexine Family by Tandem Ring-Closing Metathesis−Transannular Cyclization. (+)-Australine

2. Birch Reduction of Electron-Deficient Pyrroles

3. Reduction of electron-deficient pyrroles using group I and II metals in ammonia

4. Stereoselective reductive alkylation of 2,5-disubstituted pyrroles: a role for naphthalene in the partial reduction of heterocycles

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