105803-40-5Relevant academic research and scientific papers
Application of Bakers' Yeast Mediated Reductions of Bicyclooct-2-en-7-ones to the Enantioselective Synthesis of Prostacyclin Analogues
Keretesz, Denis J.,Kluge, Arthur F.
, p. 4962 - 4968 (1988)
Reduction of 8,8-dichlorobicyclooct-2-en-7-one (14) with bakers' yeast gave (1R,6S,7S)-8,8-dichlorobicyclooct-2-en-7-ol and (1S,6R)-8,8-dichlorobicyclooct-2-en-7-one in high optical purities and 27percent and 14perce
Potent Prostacyclin Analogues Based on the Bicyclooctane Ring System
Kluge, Arthur F.,Kertesz, Denis J.,O-Yang, Counde,Wu, Helen Y.
, p. 2860 - 2868 (2007/10/02)
The novel and biologically active prostacyclin mimetics 2 and 29 were prepared in a sequence based on the regioselective opening of epoxide 7 with a lithium acetylide in the presence of boron trifluoride etherate.The regioselectivity of epoxide opening wa
Novel [4,2,0]bicyclooctane derivatives with valuable therapeutic properties
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, (2008/06/13)
Compounds useful in treating cardiovascular disorders such as thrombosis, hypertension, and atherosclerosis are compounds depicted in formulas (1), (2), and (3): STR1 wherein: n is 2 or 3; R1 is CH2 OH, CHO, CO2 R or CO2 H; R2 is hydrogen or methyl; and R3 is linear or branched alkyl having 5-10 carbon atoms, STR2 optionally substituted with lower alkyl, lower alkoxy, trifluoromethyl, or halogen, in which a is 0, 1 or 2; b is 3-7; m is 1 or 2; and R is STR3 in which each R4 is independently hydrogen or lower alkyl having 1-6 carbon atoms, and the pharmaceutically acceptable, non-toxic salts and esters thereof.
