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

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

doi:10.1002/bscb.19860951108

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

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

Chemistry

Research output: Contribution to journal › Article › peer-review

5 Scopus citations

Abstract

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

Original language	English (US)
Pages (from-to)	1021-1031
Number of pages	11
Journal	Bulletin des Sociétés Chimiques Belges
Volume	95
Issue number	11
DOIs	https://doi.org/10.1002/bscb.19860951108
State	Published - 1986

All Science Journal Classification (ASJC) codes

Chemistry(all)

Access to Document

10.1002/bscb.19860951108

Cite this

@article{09ca7c654ba34be98ef1e427cbab85f7,

title = "Applications of N‐Sulfinyl Dienophile Diels‐Alder Cycloadditions to Synthesis of Unusual Amino Sugars",

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

author = "Weinreb, {Steven M.} and Gainor, {James A.} and Joyce, {Richard P.}",

year = "1986",

doi = "10.1002/bscb.19860951108",

language = "English (US)",

volume = "95",

pages = "1021--1031",

journal = "Bulletin des Soci{\'e}t{\'e}s Chimiques Belges",

issn = "0037-9646",

publisher = "John Wiley and Sons Ltd",

number = "11",

}

TY - JOUR

T1 - Applications of N‐Sulfinyl Dienophile Diels‐Alder Cycloadditions to Synthesis of Unusual Amino Sugars

AU - Weinreb, Steven M.

AU - Gainor, James A.

AU - Joyce, Richard P.

PY - 1986

Y1 - 1986

N2 - The amino sugar moieties of staurosporine and nogalarol have been stereospecifically synthesized by a strategy utilizing N‐sulfinyl Diels‐Alder chemistry.

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

UR - http://www.scopus.com/inward/record.url?scp=84919142129&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84919142129&partnerID=8YFLogxK

U2 - 10.1002/bscb.19860951108

DO - 10.1002/bscb.19860951108

M3 - Article

AN - SCOPUS:84919142129

SN - 0037-9646

VL - 95

SP - 1021

EP - 1031

JO - Bulletin des Sociétés Chimiques Belges

JF - Bulletin des Sociétés Chimiques Belges

IS - 11

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this