Synthesis of labile all-trans-7,8,7′,8′-bis-acetylenic carotenoids by bi-directional Horner–Wadsworth–Emmons condensation

Author:

Vaz Belén12345,Fontán Noelia12345,Castiñeira Marta12345,Álvarez Rosana12345,de Lera Ángel R.12345

Affiliation:

1. Department of Organic Chemistry and Center for Biomedical Research (CINBIO)

2. IBIV

3. Universidade de Vigo

4. 36310 Vigo

5. Spain

Abstract

Two symmetrical C7,C8-acetylenic carotenoids have been stereoselectively prepared using a bi-directional Horner–Wadsworth–Emmons condensation of the C10-dialdehyde and C15-phosphonates.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference49 articles.

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3. Carotenoids. Part 1B. Spectroscopy, ed. G. Britton, S. Liaaen-Jensen and H. Pfander, Birkhäuser, Basel, 1995

4. G. Britton , S.Liaaen-Jensen and H.Pfander, Carotenoids. Vol. 4. Natural Functions, Birkhäuser, Basel, 2008

5. Reaction Dynamics of Flavonoids and Carotenoids as Antioxidants

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