161068-69-5Relevant articles and documents
Synthesis of 5-(3-indolyl)oxazole natural products. Structure revision of Almazole D
Miyake, Fumiko,Hashimoto, Michinao,Tonsiengsom, Sorasaree,Yakushijin, Kenichi,Horne, David A.
experimental part, p. 4888 - 4893 (2010/08/06)
The synthesis and utility of β-oxotryptamine and β-oxytryptophan ester synthons provide a convenient entry to 5-(3-indolyl)oxazole natural products leading to a structure revision of almazole D.
Almazole C, a new indole alkaloid bearing an unusually 2,5-disubstituted oxazole moiety, and its putative biogenetic peptidic precursors, from a Senegalese delesseriacean seaweed
Guella,Mancini,N'Diaye,Pietra
, p. 1999 - 2006 (2007/10/02)
From product isolation and biomimetic synthesis - which also establishes absolute configurations - the known oxazole alkaloids almazoles A ((+)-1) and B ((+)-2) seem to arise in a Senegalese delesseriacean seaweed from, in sequence, the new modified pepti