Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/xmlui/handle/10054/10789
Title: Enantiospecific synthesis of [7R,6S,5S,4R]-triacetoxy-(-)-goniotriol
Authors: SRIKANTH, GSC
KRISHNA, UM
TRIVEDI, GK
Keywords: Goniothalamus-Giganteus Annonaceae
Styryl-Lactones
(+)-Goniofufurone
(+)-Goniotriol
Goniofufurone
Issue Date: 2002
Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Citation: TETRAHEDRON LETTERS, 43(31), 5471-5473
Abstract: A short and efficient synthesis of [7R,6S,5S,4R]-triacetoxy-(-)-goniotriol starting form D-glucose is described. A sequence of ring closing metathesis (RCM) followed by a PCC oxidation was used to construct the core six-membered alpha,beta-unsaturated lactone moiety. (C) 2002 . .
URI: http://dx.doi.org/10.1016/S0040-4039(02)01048-1
http://dspace.library.iitb.ac.in/xmlui/handle/10054/10789
http://hdl.handle.net/10054/10789
ISSN: 0040-4039
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