Synthesis of a lactone natural product found in Greek tobacco
摘要:
A short and stereoselective synthesis of (3R*,4R*,7R*)-3,7-epoxy-4,8-dimethyl-8-nonen-4-olide, a natural product isolated from cured tobacco leaves, has been completed in six steps and 22% overall yield. A samarium(II) iodide mediated reductive cyclisation has been used to construct the functionalised tetrahydropyranol core and subsequent sequential stereoselective addition of methyllithium and lactonisation furnished the natural product. (c) 2007 Elsevier Ltd. All rights reserved.
Synthesis of a lactone natural product found in Greek tobacco
摘要:
A short and stereoselective synthesis of (3R*,4R*,7R*)-3,7-epoxy-4,8-dimethyl-8-nonen-4-olide, a natural product isolated from cured tobacco leaves, has been completed in six steps and 22% overall yield. A samarium(II) iodide mediated reductive cyclisation has been used to construct the functionalised tetrahydropyranol core and subsequent sequential stereoselective addition of methyllithium and lactonisation furnished the natural product. (c) 2007 Elsevier Ltd. All rights reserved.