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pro vyhledávání: '"Patrick Rabe"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2317-2324 (2016)
The stereochemical course of the cyclisation reaction catalysed by the bacterial 1,8-cineol synthase from Streptomyces clavuligerus was investigated using stereospecifically deuterated substrates. In contrast to the well investigated plant enzyme fro
Externí odkaz:
https://doaj.org/article/c616bf18a409451ea9d208536603b02a
Autor:
Patrick Rabe, Jeroen S. Dickschat
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1380-1394 (2016)
Farnesyl diphosphate (FPP) and all fifteen positional isomers of (13C1)FPP were enzymatically converted by the bacterial terpene cyclases corvol ether synthase from Kitasatospora setae, the epi-cubebol synthase from Streptosporangium roseum, and the
Externí odkaz:
https://doaj.org/article/f6f57cceded2401a9a5d0f9935e38c71
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2317-2324 (2016)
The stereochemical course of the cyclisation reaction catalysed by the bacterial 1,8-cineol synthase from Streptomyces clavuligerus was investigated using stereospecifically deuterated substrates. In contrast to the well investigated plant enzyme fro