An approach to the aryl-C-glycoside DEF-ring system of nogalamycin

Richard P. Joyce; M. Parvez; Steven M. Weinreb

doi:10.1016/S0040-4039(00)85088-1

An approach to the aryl-C-glycoside DEF-ring system of nogalamycin

Richard P. Joyce, M. Parvez, Steven M. Weinreb

Chemistry

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

27 Scopus citations

Abstract

Ketone 16, a key intermediate in synthesis of the nogalamycin DEF-rings, has been efficiently and stereospecifically synthesized in nine steps using a strategy centered on an intramolecular N-sulfinyl dienophile Diels-Alder cycloaddition.

Original language	English (US)
Pages (from-to)	4885-4888
Number of pages	4
Journal	Tetrahedron Letters
Volume	27
Issue number	40
DOIs	https://doi.org/10.1016/S0040-4039(00)85088-1
State	Published - 1986

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)85088-1

Cite this

@article{6849d62b3dc542f59ccddae1580c83c8,

title = "An approach to the aryl-C-glycoside DEF-ring system of nogalamycin",

abstract = "Ketone 16, a key intermediate in synthesis of the nogalamycin DEF-rings, has been efficiently and stereospecifically synthesized in nine steps using a strategy centered on an intramolecular N-sulfinyl dienophile Diels-Alder cycloaddition.",

author = "Joyce, {Richard P.} and M. Parvez and Weinreb, {Steven M.}",

year = "1986",

doi = "10.1016/S0040-4039(00)85088-1",

language = "English (US)",

volume = "27",

pages = "4885--4888",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "40",

}

TY - JOUR

T1 - An approach to the aryl-C-glycoside DEF-ring system of nogalamycin

AU - Joyce, Richard P.

AU - Parvez, M.

AU - Weinreb, Steven M.

PY - 1986

Y1 - 1986

N2 - Ketone 16, a key intermediate in synthesis of the nogalamycin DEF-rings, has been efficiently and stereospecifically synthesized in nine steps using a strategy centered on an intramolecular N-sulfinyl dienophile Diels-Alder cycloaddition.

AB - Ketone 16, a key intermediate in synthesis of the nogalamycin DEF-rings, has been efficiently and stereospecifically synthesized in nine steps using a strategy centered on an intramolecular N-sulfinyl dienophile Diels-Alder cycloaddition.

UR - http://www.scopus.com/inward/record.url?scp=0041021864&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0041021864&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)85088-1

DO - 10.1016/S0040-4039(00)85088-1

M3 - Article

AN - SCOPUS:0041021864

SN - 0040-4039

VL - 27

SP - 4885

EP - 4888

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 40

ER -

An approach to the aryl-C-glycoside DEF-ring system of nogalamycin

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this