Applications of N‐Sulfinyl Dienophile Diels‐Alder Cycloadditions to Synthesis of Unusual Amino Sugars

Steven M. Weinreb, James A. Gainor, Richard P. Joyce

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

The amino sugar moieties of staurosporine and nogalarol have been stereospecifically synthesized by a strategy utilizing N‐sulfinyl Diels‐Alder chemistry.

Original languageEnglish (US)
Pages (from-to)1021-1031
Number of pages11
JournalBulletin des Sociétés Chimiques Belges
Volume95
Issue number11
DOIs
StatePublished - Jan 1 1986

Fingerprint

Amino Sugars
Staurosporine
Cycloaddition

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Weinreb, Steven M. ; Gainor, James A. ; Joyce, Richard P. / Applications of N‐Sulfinyl Dienophile Diels‐Alder Cycloadditions to Synthesis of Unusual Amino Sugars. In: Bulletin des Sociétés Chimiques Belges. 1986 ; Vol. 95, No. 11. pp. 1021-1031.
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Applications of N‐Sulfinyl Dienophile Diels‐Alder Cycloadditions to Synthesis of Unusual Amino Sugars. / Weinreb, Steven M.; Gainor, James A.; Joyce, Richard P.

In: Bulletin des Sociétés Chimiques Belges, Vol. 95, No. 11, 01.01.1986, p. 1021-1031.

Research output: Contribution to journalArticle

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