Cycloaddition reactions of carbohydrate derivatives. Part 7

[3+2] cycloadditions of chiral nitrilimines

Attila Agócs, A. Bényei, László Somogyi, P. Herczegh

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

The diastereoselective 1,3-dipolar cycloaddition reactions of chiral alkenes with a nitrilimine derived from D-galactose phenylhydrazone were studied. The best stereoselectivity was observed with N-acryloyl-(-)-camphor sultam 9, as the chiral inductor, to produce compound 8.

Original languageEnglish
Pages (from-to)3359-3363
Number of pages5
JournalTetrahedron Asymmetry
Volume9
Issue number19
DOIs
Publication statusPublished - Oct 2 1998

Fingerprint

Camphor
camphor
galactose
Stereoselectivity
Cycloaddition
carbohydrates
Cycloaddition Reaction
cycloaddition
Alkenes
inductors
Carbohydrates
Galactose
alkenes
Olefins
Derivatives
phenylhydrazone
naphthosultone

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Organic Chemistry
  • Materials Chemistry
  • Drug Discovery

Cite this

Cycloaddition reactions of carbohydrate derivatives. Part 7 : [3+2] cycloadditions of chiral nitrilimines. / Agócs, Attila; Bényei, A.; Somogyi, László; Herczegh, P.

In: Tetrahedron Asymmetry, Vol. 9, No. 19, 02.10.1998, p. 3359-3363.

Research output: Contribution to journalArticle

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