103795-36-4Relevant articles and documents
Stereoselective total synthesis of (-)-brevisamide
Yadav,Reddy, N. Mallikarjuna,Rahman, Md. Ataur,Prasad,Reddy, B.V. Subba
, p. 8618 - 8625 (2013/09/12)
The stereoselective total synthesis of (-)-brevisamide, a novel marine cyclic ether alkaloid isolated from dinoflagellate karenia brevis is described. The key steps involved in this synthesis are the Sharpless asymmetric epoxidation and regioselective rin
Complete structure of the mycolactones [10]
Fidanze,Song,Szlosek-Pinaud,Small,Kishi
, p. 10117 - 10118 (2007/10/03)
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Asymmetric Synthesis of ent-Corey Lactone Alcohol and its 12-(all-cys)- and 11-Epimers via Free Radical 5-exo-trig-C,C Cyclization
Mulzer, Johann,Kermanchahi, Abdul Kader,Buschmann, Juergen,Luger, Peter
, p. 531 - 540 (2007/10/02)
Asymmetric eight-step syntheses are reported for the ent-Corey lactone alcohol derivatives 3a-d and their epimers 4a-d and 14a, b from (R)-2,3-isopropylidene glyceraldehyde (5) as the starting material.The key step of the synthesis is the free radical cyc