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Studies directed towards the total synthesis of clavosolides: synthesis of an isomer of clavosolide A
Authors:Tushar Kanti Chakraborty  Vakiti Ramkrishna Reddy
Affiliation:Indian Institute of Chemical Technology, Hyderabad 500 007, India
Abstract:The total synthesis of clavosolide A, employing a radical-mediated route to build its substituted tetrahydropyran unit, a Yamaguchi reaction to construct the diolide aglycon and the Schmidt method for the final glycosidation step, revealed that the reported structure is an isomer of the natural product.
Keywords:Clavosolides   Clavosolide A   Epoxide opening   2-Methyl-1,3-diol   Diolide
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