Enantioselective N-sulfinyl dienophile diels-alder cycloadditions

Stacy W. Remiszewski, Joongik Yang, Steven M. Weinreb

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

N-Sulfinyl carbamates prepared from phenylmenthol (1) and (+) -camphor- derived alcohol 10 display high enantioselectivity in TiCl4 catalyzed [4+2] cycloadditions with 1,3-cyclohexadiene.

Original languageEnglish (US)
Pages (from-to)1853-1856
Number of pages4
JournalTetrahedron Letters
Volume27
Issue number17
DOIs
StatePublished - Jan 1 1986

Fingerprint

Camphor
Carbamates
Cycloaddition
Enantioselectivity
Cycloaddition Reaction
Alcohols
1,3-cyclohexadiene
titanium tetrachloride

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Remiszewski, Stacy W. ; Yang, Joongik ; Weinreb, Steven M. / Enantioselective N-sulfinyl dienophile diels-alder cycloadditions. In: Tetrahedron Letters. 1986 ; Vol. 27, No. 17. pp. 1853-1856.
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Enantioselective N-sulfinyl dienophile diels-alder cycloadditions. / Remiszewski, Stacy W.; Yang, Joongik; Weinreb, Steven M.

In: Tetrahedron Letters, Vol. 27, No. 17, 01.01.1986, p. 1853-1856.

Research output: Contribution to journalArticle

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