Title of article
Total syntheses of 28,29-diepi-arenamide A, 29-epi-arenamide A, and 28-epi-arenamide A
Author/Authors
Jithender Reddy، نويسنده , , V. and Pradhan، نويسنده , , Tapan Kumar and Ghosh، نويسنده , , Subhash، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2012
Pages
3
From page
6148
To page
6150
Abstract
This communication describes the synthesis of stereochemical analogs of arenamide A, a 19-membered cytotoxic depsipeptide isolated from the fermentation broth of a marine bacterial strain Salinispora arenicola. The key steps are diastereoselective aldol reaction, Mitsunobu reaction, and HATU mediated macrolactamization.
Keywords
Arenamide A , Salinispora arenicola , Depsipeptides , Cytotoxic , macrolactamization
Journal title
Tetrahedron Letters
Serial Year
2012
Journal title
Tetrahedron Letters
Record number
1882630
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