Lewis acid and high pressure promoted Diels-Alder cycloadditions of N-alkyl-N-sulfinyl dienophiles

Scott I. Bell, Steven M. Weinreb

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Normally unreactive N-alkyl-N-sulfinyl compounds act as dienophiles in both inter and intramolecular Diels-Alder processes in the presence of Lewis acids or optimally under high pressure.

Original languageEnglish (US)
Pages (from-to)4233-4236
Number of pages4
JournalTetrahedron Letters
Volume29
Issue number34
DOIs
StatePublished - Jan 1 1988

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Lewis Acids
Cycloaddition
Cycloaddition Reaction
Pressure

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Bell, Scott I. ; Weinreb, Steven M. / Lewis acid and high pressure promoted Diels-Alder cycloadditions of N-alkyl-N-sulfinyl dienophiles. In: Tetrahedron Letters. 1988 ; Vol. 29, No. 34. pp. 4233-4236.
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Lewis acid and high pressure promoted Diels-Alder cycloadditions of N-alkyl-N-sulfinyl dienophiles. / Bell, Scott I.; Weinreb, Steven M.

In: Tetrahedron Letters, Vol. 29, No. 34, 01.01.1988, p. 4233-4236.

Research output: Contribution to journalArticle

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