A short approach to chaetomellic anhydride A from 2,2-dichloropalmitic acid: elucidation of the mechanism governing the functional rearrangement of the chlorinated pyrrolidin-2-one intermediate-Reference-Cited by-同舟云学术

A short approach to chaetomellic anhydride A from 2,2-dichloropalmitic acid: elucidation of the mechanism governing the functional rearrangement of the chlorinated pyrrolidin-2-one intermediate

Published:2006-01 Issue:4 Volume:62 Page:746-757
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Bellesia Franco,Danieli Chiara,Buyck Laurent De,Galeazzi Roberta,Ghelfi Franco,Mucci Adele,Orena Mario,Pagnoni Ugo M.,Parsons Andrew F.,Roncaglia Fabrizio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference50 articles.

1. Isolation and structure of chaetomellic acids A and B from Chaetomella acutiseta: farnesyl pyrophosphate mimic inhibitors of ras farnesyl-protein transferase

2. Efficient syntheses, human and yeast farnesyl-protein transferase inhibitory activities of chaetomellic acids and analogues

3. Synthesis and biological activity of isopentenyl diphosphate analogues

4. Protein farnesyltransferase inhibitors interfere with farnesyl diphosphate binding by rubber transferase

5. Synthesis of mono- and disaccharide analogs of moenomycin and lipid II for inhibition of transglycosylase activity of penicillin-binding protein 1b

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