A versatile and highly stereocontrolled synthetic approach to homochiral polyfunctional norbornene and norbornane derivatives

Ramon Casas, Javier Ibarzo, José M. Jiménez, Rosa M. Ortuño

Research output: Contribution to journalArticleResearchpeer-review

9 Citations (Scopus)

Abstract

Several title compounds have been synthesized from D-mannitol as the unique chiral precursor. The target molecules include pairs of enantiomers and their configuration has mainly been assured by controlling the facial and the endo/exo diastereoselectivity in the Diels-Alder reactions of chiral cyclic or acyclic dienophiles. Some of the products obtained are key intermediates in the synthesis of biologically active compounds. © 1993.
Original languageEnglish
Pages (from-to)669-680
JournalTetrahedron: asymmetry
Volume4
Issue number4
DOIs
Publication statusPublished - 1 Jan 1993

Fingerprint Dive into the research topics of 'A versatile and highly stereocontrolled synthetic approach to homochiral polyfunctional norbornene and norbornane derivatives'. Together they form a unique fingerprint.

Cite this