Efficient synthetic access to a new family of highly potent bryostatin analogues via a Prins-driven macrocyclization strategy. [electronic resource]
- Journal of the American Chemical Society May 2008
- 6658-9 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural
1520-5126
10.1021/ja8015632 doi
Bryostatins--chemical synthesis Macrocyclic Compounds--chemical synthesis Protein Kinase C--chemistry