Title of article
Studies directed towards the total synthesis of clavosolides: synthesis of an isomer of clavosolide A
Author/Authors
Chakraborty، نويسنده , , Tushar Kanti and Reddy، نويسنده , , Vakiti Ramkrishna Reddy، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2006
Pages
4
From page
2099
To page
2102
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 , 2-Methyl-1 , Epoxide opening , Diolide , 3-diol
Journal title
Tetrahedron Letters
Serial Year
2006
Journal title
Tetrahedron Letters
Record number
1849321
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