Accessibility navigation

A homo-proline tetrazole as an improved organocatalyst for the asymmetric Michael addition of carbonyl compounds to nitro-olefins

Lists
Tools

Mitchell, C.E.T., Cobb, A.J.A. and Ley, S.V. (2005) A homo-proline tetrazole as an improved organocatalyst for the asymmetric Michael addition of carbonyl compounds to nitro-olefins. Synlett (4). pp. 611-614. ISSN 0936-5214

Full text not archived in this repository.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

To link to this item DOI: 10.1055/s-2005-862392

Abstract/Summary

A new homo-proline tetrazole derivative 7 has been prepared and shown to have improved properties for achieving asymmetric Michael addition of carbonyl compounds to nitro-olefins.

Item Type:Article
Refereed:Yes
Divisions:Life Sciences > School of Chemistry, Food and Pharmacy > School of Pharmacy
ID Code:13687
Uncontrolled Keywords:asymmetric, nitro-Michael, organocatalysis, homoproline, tetrazole , MANNICH-TYPE REACTIONS, AMINO-ACID DERIVATIVES, ALPHA-AMINO, ONE-POT, ALDEHYDE DONORS, ALDOL REACTIONS, KETONES, 5-PYRROLIDIN-2-YLTETRAZOLE, NITROOLEFINS, NITROSTYRENE
Altmetric
Deposit Details

University Staff: Request a correction | Centaur Editors: Update this record

Page navigation

See also