| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274528 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
The C15-C27 segment of venturicidins was stereoselectively synthesized by using two types of stereospecific methyl substitution reactions of epoxides and subsequent stereocontrolled methylation reactions of lactone derivatives as the key steps.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yuji Suzuki, Shinji Nagumo, Eiko Yasui, Megumi Mizukami, Masaaki Miyashita,