Synthesis of stereochemically defined (E)-cinnamyl alcohol derivatives from the Baylis-Hillman adducts

Authors
Kim, HS Kim, TY Lee, KY Chung, YM Lee, HJ Kim, JN
Citation
Hs. Kim et al., Synthesis of stereochemically defined (E)-cinnamyl alcohol derivatives from the Baylis-Hillman adducts, TETRAHEDR L, 41(15), 2000, pp. 2613-2616
Citations number
21
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
15
Year of publication
2000
Pages
2613 - 2616
Database
ISI
SICI code
0040-4039(20000408)41:15<2613:SOSD(A>2.0.ZU;2-7
Abstract
The reaction of the Baylis-Hillman adducts 1a-g and trifluoroacetic acid at 30-70 degrees C gave the rearranged cinnamyl alcohols 2a-g stereoselective ly in moderate yields. (C) 2000 Elsevier Science Ltd. All rights reserved.