Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5216666 | Tetrahedron | 2014 | 7 Pages |
Abstract
A flexible protocol for the synthesis of three lipophilic α-amino acid components of some novel cyclic peptides having important histone deacetylase inhibiting properties has been developed from a common source, which featured a cross-metathesis reaction between two unhindered terminal olefins as the key step.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Amit K. Pahari, Jyoti Prasad Mukherjee, Shital K. Chattopadhyay,