Enantioselective organocatalytic transfer hydrogenation of α-imino esters by utilization of benzothiazoline as highly efficient reducing agent
Benzothiazoline was employed as an efficient and versatile reducing agent for the chiral phosphoric acid-catalyzed transfer hydrogenation of α-imino esters. The corresponding α-amino esters were furnished with excellent enantioselectivities. Novel and rea
Zhu, Chen,Akiyama, Takahiko
supporting information; experimental part
p. 1846 - 1850
(2010/11/03)
Benzothiazoline: highly efficient reducing agent for the enantioselective organocatalytic transfer hydrogenation of ketimines
Benzothiazoline proved to be an efficient reducing agent for the phosphoric acid-catalyzed enantloselectlve transfer hydrogenation reaction of imines. Corresponding amines were obtained with excellent enantioselectivities.
Zhu, Chen,Aklyama, Takahlko
supporting information; experimental part
p. 4180 - 4183
(2009/12/30)
Control of acarids using certain benzothiazoles or benzothiazolines
Compounds having either of the structures SPC1 Have strong acaricidal activity, in which R is a phenyl or naphthyl group, or phenyl with certain designated substitution. Thus, mites may be controlled on such crops as cotton by applying such compounds as 2-(1-naphthyl)benzothiazoline or 2-(5-t-butyl-2-hydroxyphenyl)benzothiazole.
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(2008/06/13)
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