667865-89-6Relevant academic research and scientific papers
Stereoselective Formal Synthesis of (-)-Salicylihalamides A and B Via Prins Cyclisation
Yadav,Venkateswar Rao,Purushothama Rao,Sridhar Reddy,Prasad
, p. 457 - 460 (2011/09/14)
A stereoselective and convergent formal approach to Salicylihalamide A and B is achieved through our recently developed strategy for the construction of polyketide precursors via Prins cyclisation. The approach mainly relies upon reductive opening of 1-iodomethyl cyclic ethers, Mitsunobu inversion and ring closing metathesis along with Prins cyclisation.
Formal total synthesis of (-)-salicylihalamides A and B
Yadav,Srihari
, p. 81 - 89 (2007/10/03)
Formal total synthesis of (-)-salicylihalamides A and B is described starting with a nonracemic chiral epoxide obtained from Jacobsen's kinetic resolution. Sharpless asymmetric epoxidation, Diels Alder reaction, Mitsunobu coupling and ring closing metathe
