Literature DB >> 16609790

Possibility of a non-amino acid pathway in the biosynthesis of marine-derived oxazoles.

Takao Ichino1, Hirokazu Arimoto, Daisuke Uemura.   

Abstract

A novel avenue for oxazoles via Beckmann rearrangement of alpha-formyl ketoxime dimethyl acetals is described that indicates the possibility of a non-amino acid biosynthetic pathway in marine natural products.

Entities:  

Mesh：

Substances：

Year:  2006        PMID： 16609790     DOI： 10.1039/b517149k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  3 in total

Review 1.  Recent N-atom containing compounds from indo-pacific invertebrates.

Authors:  Yoel Kashman; Ashgan Bishara; Maurice Aknin
Journal:  Mar Drugs       Date:  2010-11-10       Impact factor: 5.118

2.  Structure and Biosynthesis of Myxofacyclines: Unique Myxobacterial Polyketides Featuring Varing and Rare Heterocycles[] *.

Authors:  Alexander Popoff; Joachim J Hug; Sebastian Walesch; Ronald Garcia; Lena Keller; Rolf Müller
Journal:  Chemistry       Date:  2021-11-05       Impact factor: 5.020

Review 3.  Selected synthetic strategies to cyclophanes.

Authors:  Mukesh Eknath Shirbhate; Gopalkrushna T Waghule; Sambasivarao Kotha
Journal:  Beilstein J Org Chem       Date:  2015-07-29       Impact factor: 2.883
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.