Synthesis of isoflavonoids. Enantiopure cis- and trans-6a-hydroxypterocarpans and a racemic trans-pterocarpan

Authors
van Aardt, TG van Rensburg, H Ferreira, D
Citation
Tg. Van Aardt et al., Synthesis of isoflavonoids. Enantiopure cis- and trans-6a-hydroxypterocarpans and a racemic trans-pterocarpan, TETRAHEDRON, 57(33), 2001, pp. 7113-7126
Citations number
44
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
57
Issue
33
Year of publication
2001
Pages
7113 - 7126
Database
ISI
SICI code
0040-4020(20010813)57:33<7113:SOIECA>2.0.ZU;2-Y
Abstract
Aldol condensation between phenylacetates and benzaldehydes affords 2,3-dia ryl-3-hydroxypropanoates which serve as common precursors to both the first racemic trans-pterocarpan and enantiopure cis- and trans-6a-hydroxypteroca rpans. (C) 2001 Elsevier Science Ltd. All rights reserved.