Abstract
Sanjoinine-G1 (1), a 14-membered cyclopeptide, was synthesized with stereoselective reactions. Started from d-serine, a cyclic precursor for various frangulanine type 14-membered cyclopeptide alkaloids was synthesized and the side chain acylation product was identical with the natural sanjoinine-G1 (17 steps, overall yield 1.36%).
Original language | English |
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Pages (from-to) | 1909-1914 |
Number of pages | 6 |
Journal | Heterocycles |
Volume | 41 |
Issue number | 9 |
DOIs | |
State | Published - 1 Sep 1995 |