921207-77-4Relevant articles and documents
Towards the synthesis of Palmerolide A: asymmetric synthesis of C1-C14 fragment
Chandrasekhar,Vijeender,Chandrashekar,Raji Reddy
, p. 2473 - 2478 (2008/03/13)
The synthesis of a C1-C14 fragment of a marine cytotoxic natural product Palmerolide A is described. The key steps involved in this synthesis are deoxygenative rearrangement of an alkynol followed by an asymmetric dihydroxylation of a diene ester and CBS-