Document Detail


Synthesis of the ABH rings of ecteinascidin 597 using a connective Pummerer-type cyclisation.
MedLine Citation:
PMID:  21863175     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
A connective Pummerer-type cyclisation involving a cysteine derivative and an N-benzyl glyoxamide 3 has been applied in an asymmetric synthesis of the protected ABH rings 2 of the antitumour and antimicrobial natural product ecteinascidin 597.
Authors:
Laura H S Smith; Trung Thanh Nguyen; Helen F Sneddon; David J Procter
Related Documents :
20045245 - Catalytic wet oxidation of thiocyanate with homogeneous copper(ii) sulphate catalyst.
17768005 - Use of an amorphous iron oxide hydrated as catalyst for hydrogen peroxide oxidation of ...
11674535 - Studies on the mechanism of action of 2-formyl-4-pyrrolidinopyridine: isolation and cha...
23815585 - Oxadiazole derivatives as potential biological agents.
22371225 - One-pot sequential ti-/cu-catalysis for tandem amidation/ullmann-type cyclization: synt...
22114475 - Cytotoxicity of naphthoquinones and their capacity to generate reactive oxygen species ...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-8-24
Journal Detail:
Title:  Chemical communications (Cambridge, England)     Volume:  -     ISSN:  1364-548X     ISO Abbreviation:  -     Publication Date:  2011 Aug 
Date Detail:
Created Date:  2011-8-24     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9610838     Medline TA:  Chem Commun (Camb)     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
School of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK. david.j.procter@manchester.ac.uk.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  [60]Fullerene-based monolayers as neuroprotective biocompatible hybrid materials.
Next Document:  Intrastrand locks increase duplex stability and base pairing selectivity.