Biomimetic One-Step Access to Nitraramine from Simple C5 Units. Revision of the Previously Reported Structure of Epinitraramine to Nitraramine-Reference-Cited by-同舟云学术

Biomimetic One-Step Access to Nitraramine from Simple C5 Units. Revision of the Previously Reported Structure of Epinitraramine to Nitraramine

Published:2005-05-17 Issue:12 Volume:7 Page:2497-2499
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Gravel Edmond¹,Poupon Erwan¹,Hocquemiller Reynald¹

Affiliation:

1. Laboratoire de Pharmacognosie associé au CNRS (UMR 8076, BioCIS), Centre d'Études Pharmaceutiques, Université Paris−Sud 11, 5, rue Jean-Baptispte Clément, 92290 Châtenay-Malabry, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol050849q

Reference12 articles.

1. Wanner, M. J.; Koomen, G.J. InStudies in Natural ProductsChemistry: Stereoselectivity in Synthesis and Biosynthesis of Lupine andNitraria Alkaloids; Atta-ur-Rahman, Ed.; Elsevier: Amsterdam, 1994; Vol. 14, pp 731−768 and references therein.

2. Biomimetic syntheses of alkaloids based on tetrahydropyridine

3. Biomimetic Synthesis of Nitraramine

4. Expeditious Enantioselective Biomimetic Synthesis of theNitraria Alkaloids (+)-Isonitramine and (−)-Sibirine

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