78746-23-3Relevant articles and documents
Total Synthesis of Gombamide A
Garcia-Barrantes, Pedro M.,Lindsley, Craig W.
, p. 3810 - 3813 (2016/08/16)
The first total synthesis of Gombamide A (1), a cytotoxic cyclic thiopeptide from the sponge Clathria gombawuiensis, has been achieved. Highlights of the convergent synthesis feature a disulfide bond forming cascade to close the 17-membered macrocycle and a selenoazidylation procedure to access the unusual para-hydroxystyrlyamide (pHSA) moiety. The synthesis required 18 steps, 11 steps in its longest linear sequence, and proceeded in 9.1% overall yield. This work will facilitate the study of the biological effects of Gombamide A and provide groundwork to explore the structure-activity relationship around this rare natural product.
Rapid peptide synthesis in liquid phase. Preparation of angiotensin II and delta-sleep-inducing peptide by the 'hold-in' solution method
Nozaki,Muramatsu
, p. 2165 - 2168 (2007/10/02)
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