Steric constraints against [3,3]-sigmatropic rearrangement of allylic azides. A convenient approach to β-L-4-aminopent-2-enoglyceropyranosides

Cristiana Fava, Roberta Galeazzi, Giovanna Mobbili, Mario Orena

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Starting from alkyl α-D-4-0-methanesulphonylpent-2-enoglyceropyranosides 13a-c, nucleophilic substitution carried out with polymer-supported azide ion led to regioisomeric mixtures of the azides 14a-c and 15a-c. An analogous result, due to a [3,3]-sigmatropic rearrangement, was observed starting from methyl α-D-hex-2-enoerythropyranosides derivatives 6a and 6b. On the contrary, starting from alkyl β-D-4-0-methanesulphonylpent-2-enoglyceropyranosides 21a-c, azides 22a-c were exclusively obtained, and subsequently converted into the corresponding amino derivatives 23a-c. The behaviour of β-anomers 21a-c was ascribed to steric interactions in the cyclic transition state, as supported by ab initio calculations.

Original languageEnglish
Pages (from-to)2731-2741
Number of pages11
JournalTetrahedron: Asymmetry
Volume12
Issue number19
DOIs
Publication statusPublished - Oct 30 2001

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Azides
substitutes
Derivatives
polymers
ions
Substitution reactions
interactions
Polymers
Ions

ASJC Scopus subject areas

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

Cite this

Steric constraints against [3,3]-sigmatropic rearrangement of allylic azides. A convenient approach to β-L-4-aminopent-2-enoglyceropyranosides. / Fava, Cristiana; Galeazzi, Roberta; Mobbili, Giovanna; Orena, Mario.

In: Tetrahedron: Asymmetry, Vol. 12, No. 19, 30.10.2001, p. 2731-2741.

Research output: Contribution to journalArticle

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