Total synthesis of phalarine Journal Article


Authors: Li, C.; Chan, C.; Heimann, A. C.; Danishefsky, S. J.
Article Title: Total synthesis of phalarine
Abstract: (Chemical Equation Presented) End of the expedition ... for now: Completion of the first total synthesis of phalarine from an advanced rearrangement product brought up interesting obstacles to overcome. Use of the Gassman oxindole synthesis and subsequent manipulations led to the racemic natural product (see scheme, Ts = toluene-4-sulfonyl). © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
Keywords: chemistry; chemical structure; molecular structure; indoles; alkaloids; indole derivative; heterocyclic compound; models, chemical; synthesis; total synthesis; synthesis (chemical); stereoisomerism; furan derivative; furans; chemical model; organic compounds; alkaloid; nitrogen compounds; oxindoles; heterocycles; aza compounds
Journal Title: Angewandte Chemie - International Edition
Volume: 46
Issue: 9
ISSN: 1433-7851
Publisher: Wiley Blackwell  
Date Published: 2007-02-19
Start Page: 1448
End Page: 1450
Language: English
DOI: 10.1002/anie.200604072
PUBMED: 17387655
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 11" - "Export Date: 17 November 2011" - "CODEN: ACIEA" - "Source: Scopus"
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors