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游劲松, Jingsong You and John G. Verkade*
J. Org. Chem., Vol. 68, No.21, 2003,-0001,():
-1年11月30日
A new catalyst system for the synthesis of R-aryl-substituted nitriles is reported. The bicyclic triaminophosphine P(i-BuNCH2CH2) 3N (1b) serves as an efficient and versatile ligand for the palladium-catalyzed direct α-arylation of nitriles with aryl bromides. Using ligand 1b, ethyl cyanoacetate and primary as well as secondary nitriles are efficiently coupled with a wide variety of aryl bromides possessing electron-rich, electron-poor, electron-neutral, and sterically hindered groups.
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游劲松, Jing-Song You, † Ming-Yuan Shao, and Han-Mou Gau*
Organometallics 2000, 19, 3368-3373,-0001,():
-1年11月30日
Enantioselective addition of diethylzinc to aldehydes catalyzed by Ti (IV) complexes of diol derivatives of D-mannitol was carried out. Good enantioselectivities were obtained with ee values up to 86% of R-configuration. A 1H NMR study shows that the catalytic system in solution contains unreacted Ti(O-i-Pr)4, a dimeric Ti (IV) complex [Ti (O-i-Pr) 2 (μ-diolate)] 2 (4) containing two bridging diolate ligands, and a dimeric Ti (IV) complex [(diolate) (O-i-Pr)Ti-(Ì-O-i-Pr) 2 Ti (O-i-Pr) 3] (5) containing one diolate ligand attached to only one Ti (IV) metal center. The complex 5 with the more electropositive Ti (IV) metal center is considered the most active catalyst in solution. The structure of 4 was determined by X-ray analysis, and the FAB-mass spectroscopic study confirms the existence of complex 5. The role of excess Ti (O-i-Pr) 4 in the catalytic system is that Ti (O-i-Pr) 4 further reacts with the complex 4 to give the most active catalyst 5 in solution.
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【期刊论文】Chiral β-Amino Acid Derivatives via Asymmetric Hydrogenation
游劲松, Hans-Joachim Drexler, Jingsong You, Songlin Zhang, Christine Fischer, Wolfgang Baumann, Anke Spannenberg, and Detlef Heller*
Organic Process Research & Development 2003, 7, 355-361,-0001,():
-1年11月30日
This contribution gives an overview of the synthesis of chiral β-amino acids via asymmetric hydrogenation of the corresponding dehydroamino derivatives. Literature results are discussed regarding substrate synthesis and catalyst performance and how it is affected by substrate and catalyst structure as well as experimental parameters. A tentative mechanistic concept for the hydrogenation step is also presented. Scheme 1. Biologically active compounds with β-amino acid unitsa
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【期刊论文】A General Method for the Direct a-Arylation of Nitriles with Aryl Chlorides**
游劲松, Jingsong You and John G. Verkade*
Angew. Chem. Int. Ed. 2003, 42, 5051-5053,-0001,():
-1年11月30日
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【期刊论文】A Highly Active and Selective Catalyst System for the Baylis-Hillman Reaction**
游劲松, Jingsong You, Juhua Xu, and John G. Verkade*
Angew. Chem. Int. Ed. 2003, 42, 5054-5056,-0001,():
-1年11月30日
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