Effect of the allylic substituents on ring closing metathesis: the total synthesis of stagonolide B and 4-epi-stagonolide B.
National Chemical Laboratory, Dr. Homi Bhabha Road, Pune, 411 008, India.Organic & Biomolecular Chemistry (impact factor: 3.7). 01/2010; 8(2):398-406. DOI:10.1039/b916198h pp.398-406
ABSTRACT The total syntheses of stagonolide B and its 4-epimer were carried out to probe into how the relative stereochemistry of allylic hydroxy groups and their protecting groups influence the efficiency of the ring closing metathesis.
Data provided are for informational purposes only. Although carefully collected, accuracy cannot be guaranteed. The impact factor represents a rough estimation of the journal's impact factor and does not reflect the actual current impact factor. Publisher conditions are provided by RoMEO. Differing provisions from the publisher's actual policy or licence agreement may be applicable.