Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Article, Chemical Communications (Cambridge, United Kingdom) called First synthesis of an amythiamicin pyridine cluster, Author is Bagley, Mark C.; Dale, James W.; Jenkins, Robert L.; Bower, Justin, which mentions a compound: 76632-23-0, SMILESS is OCC1=CSC(C)=N1, Molecular C5H7NOS, Recommanded Product: 76632-23-0.
The pyridine-containing central domain I (SEM = CH2OCH2CH2SiMe3) of amythiamicin A (thiopeptide antibiotic) is prepared in protected form in 9 steps with 93% enantiomeric excess and 18% overall yield from (S)-2-[1-(tert-butoxycarbonylamino)-2-methylpropyl]thiazole-4-carboxylic acid. Key reaction steps were Michael addition and cyclodehydration between enamine II and propynone III.
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Reference:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem