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

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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 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.

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Item Type	Article
URI	https://reading-clone.eprints-hosting.org/id/eprint/13687
Identification Number/DOI	10.1055/s-2005-862392
Refereed	Yes
Divisions	Life Sciences > School of Chemistry, Food and Pharmacy > School of Pharmacy
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
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Date Deposited:	26 Oct 2010 16:01	Date item deposited into CentAUR
Last Modified:	13 Apr 2025 05:01	Date item last modified

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