Enantiospecific synthesis of [7R,6S,5S,4R]-triacetoxy-(-)-goniotriol
DSpace at IIT Bombay
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Title |
Enantiospecific synthesis of [7R,6S,5S,4R]-triacetoxy-(-)-goniotriol
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Creator |
SRIKANTH, GSC
KRISHNA, UM TRIVEDI, GK |
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Subject |
goniothalamus-giganteus annonaceae
styryl-lactones (+)-goniofufurone (+)-goniotriol goniofufurone styryllactones goniotriol ring closing metathesis pcc oxidation |
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Description |
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 . .
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Publisher |
PERGAMON-ELSEVIER SCIENCE LTD
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Date |
2011-08-24T06:31:35Z
2011-12-26T12:56:46Z 2011-12-27T05:45:59Z 2011-08-24T06:31:35Z 2011-12-26T12:56:46Z 2011-12-27T05:45:59Z 2002 |
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Type |
Article
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Identifier |
TETRAHEDRON LETTERS, 43(31), 5471-5473
0040-4039 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 |
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Language |
en
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