Sabitha, Gowravaram ; Vangala, Bhaskar ; Siva Sankara Reddy, S. ; Yadav, Jhillu S. (2010) Total synthesis of (+)-cryptocaryalactone and of a diastereoisomer of (+)-strictifolione via ring-closing metathesis (RCM) and olefin cross-metathesis (CM) Helvetica Chimica Acta, 93 (2). pp. 329-338. ISSN 0018-019X
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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/hlca.20...
Related URL: http://dx.doi.org/10.1002/hlca.200900170
Abstract
Ring-closing metathesis (RCM) and olefin cross-metathesis (CM) reactions were used as the key steps for the synthesis of (+)-cryptocaryalactone (1) and the first synthesis of the diastereoisomer 3 of (+)-strictifolione, starting from the commercially available L-malic acid (=(2S)-2-hydroxybutanedioic acid).
Item Type: | Article |
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Source: | Copyright of this article belongs to John Wiley and Sons. |
Keywords: | Ring-closing Metathesis; Olefin Cross-metathesis; Strictifolione; Cryptocaryalactone; Grubbs catalyst |
ID Code: | 62873 |
Deposited On: | 24 Sep 2011 05:01 |
Last Modified: | 24 Sep 2011 05:01 |
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