58677-60-4Relevant academic research and scientific papers
Biomimetic Asymmetric Reduction of Tetrasubstituted Olefin 2,3-Disubstituted Inden-1-ones with Chiral and Regenerable NAD(P)H Model CYNAM
Ding, Yi-Xuan,Wu, Bo,Zhou, Yong-Gui,Zhu, Zhou-Hao
supporting information, p. 7166 - 7170 (2021/09/22)
Because of the formidable development of the asymmetric reduction of tetrasubstituted olefins, an effective method is in urgent demand. Herein, through the biomimetic protocol of the coenzyme NAD(P)H, the reduction of tetrasubstituted olefin 2,3-substitut
Isoquinolone derivatives, their production and use
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, (2008/06/13)
A compound of the formula (I): STR1 wherein X is --CH2 -CH2 -- or --CH=CH--, Y is STR2 Z is an oxygen or sulfur atom, R1 and R2 are independently a hydrogen atom, an optionally substituted hydrocarbon group or a
