z-logo
Premium
Synthese von Carotinoiden mit hydroxylierter Methylgruppe an der Polyenkette mit Hilfe von Vinyl‐Anionen ( Shapiro ‐Reaktion)
Author(s) -
Bütikofer PierreAndré,
Eugster Conrad Hans
Publication year - 1983
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19830660418
Subject(s) - chemistry , hydroxymethyl , optically active , medicinal chemistry , stereochemistry , organic chemistry
Syntheses of Hydroxymethyl‐carotenoids Using Vinyl‐Anions Generated by the Shapiro ‐Reaction A versatile synthesis of hydroxymethyl‐carotenoids with β‐ or ϵ‐end groups is presented. It makes use of the reactive vinyl anions prepared by the Shapiro ‐reaction from (phenylsulfonyl)hydrazones of polyenones and their smooth 1,2‐addition to polyenals. Thus, e.g. (3 R ,6′ R )‐β, ϵ‐carotene‐3, 19‐diol ( 72 ), an optically active model compound structurally very close to loroxanthin ( 1 ), has been synthesized.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here