Literature DB >> 15932232

Biomimetic one-step access to nitraramine from simple C5 units. Revision of the previously reported structure of epinitraramine to nitraramine.

Edmond Gravel1, Erwan Poupon, Reynald Hocquemiller.   

Abstract

[reaction: see text] A single biomimetic cascade sequence featuring intermolecular followed by intramolecular cyclizations allowed the biomimetic synthesis of nitraramine from simple C5-lysine-derived metabolites. In the course of the study, the structure of epinitraramine was also revisited.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15932232     DOI: 10.1021/ol050849q

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  A Biomimetic Synthesis Elucidates the Origin of Preuisolactone A.

Authors:  Alexander J E Novak; Claire E Grigglestone; Dirk Trauner
Journal:  J Am Chem Soc       Date:  2019-09-23       Impact factor: 15.419

2.  Domino constructions of pentacyclic indeno[2,1-c]quinolines and pyrano[4,3-b]oxepines by [4+1]/[3+2+1]/[5+1] and [4+3] multiple cyclizations.

Authors:  Bo Jiang; Bao-Ming Feng; Shu-Liang Wang; Shu-Jiang Tu; Guigen Li
Journal:  Chemistry       Date:  2012-07-05       Impact factor: 5.236

3.  Imines that react with phenols in water over a wide pH range.

Authors:  Maki Minakawa; Hai-Ming Guo; Fujie Tanaka
Journal:  J Org Chem       Date:  2008-10-10       Impact factor: 4.354

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.