19888-27-8Relevant articles and documents
Mori,Matsui
, p. 4435 (1969)
The first enantioselective synthesis of the chemotactic factor sirenin by an intramolecular [2 + 1] cyclization using a new chiral catalyst
Gant,Gant, Thomas G.,Noe,Noe, Mark C.,Corey
, p. 8745 - 8748 (1995)
A simple, highly enantioselective synthesis of sirenin (1) (bioactive form) has been developed which depends on the intramolecular [2 + 1] cycloaddition reaction of diazo ester 5 to form bicyclic ester 6 (95:5 enantioselectivity) using a new and remarkably stable monomeric chiral Cu(I) complex (2) whose structure was proven by X-ray diffraction analysis.
A New Synthesis of (+/-)-Sirenin and a Physiologically Active Analogue
Harding, Kenn E.,Strickland, J. Byron,Pommerville, Jeffrey
, p. 4877 - 4883 (2007/10/02)
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A NEW TOTAL SYNTHESIS OF DL-SIRENIN
Mandai, T.,Hara, K.,Kawada, M.,Nokami, J.
, p. 1517 - 1518 (2007/10/02)
A new total synthesis of dl-sirenin (1) has been effectively accomplished by employing the acetate 4a obtained by the stereoselective rearrangenent of the acetate 3 using a palladium catalyst.