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

Joseph Sisko, Steven M. Weinreb

Research output: Contribution to journalArticle

70 Citations (Scopus)

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 languageEnglish (US)
Pages (from-to)3037-3040
Number of pages4
JournalTetrahedron Letters
Volume30
Issue number23
DOIs
StatePublished - Jan 1 1989

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Imines
Cycloaddition Reaction
Aldehydes
boron trifluoride etherate

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

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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.",
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A convenient in situ procedure for effecting inter- and intramolecular Diels-Alder reactions of N-sulfonyl imines. / Sisko, Joseph; Weinreb, Steven M.

In: Tetrahedron Letters, Vol. 30, No. 23, 01.01.1989, p. 3037-3040.

Research output: Contribution to journalArticle

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AU - Sisko, Joseph

AU - Weinreb, Steven M.

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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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