| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5284976 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
An efficient stereoselective synthesis of the C1-C10 fragment of narbonolide is reported. The stereocentres at C2, 3, 4, 5, 8 and 9 in fragment 5 can be generated via an iterative asymmetric acyl-thiazolidinethione aldol reaction, whereas the stereocentre at C6 is installed by means of Myers alkylation.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
C. Prasad Narasimhulu, Javed Iqbal, Khagga Mukkanti, Parthasarathi Das,