A convenient in situ procedure for effecting inter- and intramolecular Diels-Alder reactions of N-sulfonyl imines

Joseph Sisko; Steven M. Weinreb

doi:10.1016/S0040-4039(00)99396-1

A convenient in situ procedure for effecting inter- and intramolecular Diels-Alder reactions of N-sulfonyl imines

Joseph Sisko, Steven M. Weinreb

Chemistry

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76 Scopus citations

Abstract

Treatment of an aldehyde and a 1,3-diene with N-sulfinyl-p-toluenesulfonamide/boron trifluoride etherate leads to products of an imino Diels-Alder reaction via an N-sulfonyl imine produced in situ.

Original language	English (US)
Pages (from-to)	3037-3040
Number of pages	4
Journal	Tetrahedron Letters
Volume	30
Issue number	23
DOIs	https://doi.org/10.1016/S0040-4039(00)99396-1
State	Published - 1989

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)99396-1

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title = "A convenient in situ procedure for effecting inter- and intramolecular Diels-Alder reactions of N-sulfonyl imines",

abstract = "Treatment of an aldehyde and a 1,3-diene with N-sulfinyl-p-toluenesulfonamide/boron trifluoride etherate leads to products of an imino Diels-Alder reaction via an N-sulfonyl imine produced in situ.",

author = "Joseph Sisko and Weinreb, {Steven M.}",

year = "1989",

doi = "10.1016/S0040-4039(00)99396-1",

language = "English (US)",

volume = "30",

pages = "3037--3040",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "23",

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T1 - A convenient in situ procedure for effecting inter- and intramolecular Diels-Alder reactions of N-sulfonyl imines

AU - Sisko, Joseph

AU - Weinreb, Steven M.

PY - 1989

Y1 - 1989

N2 - Treatment of an aldehyde and a 1,3-diene with N-sulfinyl-p-toluenesulfonamide/boron trifluoride etherate leads to products of an imino Diels-Alder reaction via an N-sulfonyl imine produced in situ.

AB - Treatment of an aldehyde and a 1,3-diene with N-sulfinyl-p-toluenesulfonamide/boron trifluoride etherate leads to products of an imino Diels-Alder reaction via an N-sulfonyl imine produced in situ.

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UR - http://www.scopus.com/inward/citedby.url?scp=0001153217&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)99396-1

DO - 10.1016/S0040-4039(00)99396-1

M3 - Article

AN - SCOPUS:0001153217

SN - 0040-4039

VL - 30

SP - 3037

EP - 3040

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 23

ER -

A convenient in situ procedure for effecting inter- and intramolecular Diels-Alder reactions of N-sulfonyl imines

Abstract

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