Bibliographic Details
| Title: |
A Synthesis of Cyanolide A by Intramolecular Oxa-Michael Addition. |
| Authors: |
Bates, Roderick W.1 roderick@ntu.edu.sg, Tee Guan Lek1 |
| Source: |
Synthesis. 2014, Vol. 46 Issue 13, p1731-1738. 8p. |
| Subjects: |
Macrolide antibiotics synthesis, Michael reaction, Glycosylation, Stereoselective reactions, Barbier reactions, Metathesis reactions, Carbonylation, Grignard reagents |
| Abstract: |
A synthesis of cyanolide A, a diolide natural product, has been achieved using a diastereoselective Barbier reaction, earlystage glycosylation, and intramolecular oxa-Michael addition to form the THP ring. [ABSTRACT FROM AUTHOR] |
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| Database: |
Engineering Source |
