Flavonoids—II

Autor: M.J. Byrne, K.G. Marathe, R.N. Vidwans
Rok vydání: 1966
Předmět:
Zdroj: Tetrahedron. 22:1789-1795
ISSN: 0040-4020
DOI: 10.1016/s0040-4020(01)82252-3
Popis: Isoaurones (anhydrolactones of 2-hydroxy-α-benzylmandelic acids), trimethylanhydrohazeyl lactone 2a and its 5-methyl-4′-methoxy analogue (VI) are shown to be trans -stilbene derivatives and are isomerized to cis -compounds by pyridine. The stereochemistry has been established by a stereoselective synthesis of the derived cis -stilbene-α-carboxylic acid VII (R = CH 3 , R′ = H) and confirmed by UV and NMR studies. A mechanism for isomerization has been suggested.
Databáze: OpenAIRE