125590-91-2Relevant academic research and scientific papers
Stereoselective synthesis of a nonracemic hydronaphthalene subunit of Kijanolide
Marshall,Salovich,Shearer
, p. 2398 - 2403 (2007/10/02)
Lewis acid catalyzed Diels - Alder cyclization of the tetraenal 15 affords the endo product, hydronaphthalene 16, with high diastereoselectivity. Nonracemic 15 is prepared by addition of dienyne 5 to resolved (2S,4S)-5-[(tert -butyldimethylsilyl)oxy]-2,4-
A Stereoselective Synthesis of the Hydronaphthalene Substructure of Kijanolide
Marshall, James A.,Grote, Jonathan,Shearer, Barry
, p. 1633 - 1635 (2007/10/02)
The synthesis of a hydronaphthalene substructure of the antitumor antibiotic kijanimicin is described in which four of the seven chiral centers are introduced via a diastereoselective intramolecular Diels-Alder cyclization of an all-(E)-2,8,10,12-tetradec
