Carbon hydroxylation of alkyltetrahydropyranols: A paradigm for spiroacetal biosynthesis in Bactrocera sp.


Autoria(s): Stok, J. E.; Lang, C. S.; Schwartz, B. D.; Fletcher, M. T.; Kitching, W.; De Voss, J. J.
Data(s)

01/01/2001

Resumo

[GRAPHICS] In a number of Bactrocera species the penultimate step in the biosynthesis of spiroacetals is shown to be the hydroxylation of an alkyltetrahydropyranol followed by cyclization, The monooxygenases that catalyze this side chain hydroxylation show a strong preference for oxidation four carbons from the hemiketal center, to produce the spiroacetal, The hydroxy spiroacetals observed in Bactrocera appear to derive from direct oxidation of the parent spiroacetals and not from alternate precursors.

Identificador

http://espace.library.uq.edu.au/view/UQ:59209

Idioma(s)

eng

Publicador

American Chemical Society

Palavras-Chave #Chemistry, Organic #Fruit-flies #Fly #Secretions #Chemistry #C1 #250301 Organic Chemical Synthesis #780103 Chemical sciences
Tipo

Journal Article