M
Midori Goto
Researcher at National Institute of Advanced Industrial Science and Technology
Publications - 79
Citations - 1837
Midori Goto is an academic researcher from National Institute of Advanced Industrial Science and Technology. The author has contributed to research in topics: Crystal structure & Catalysis. The author has an hindex of 24, co-authored 79 publications receiving 1657 citations. Previous affiliations of Midori Goto include Hunan University & Xiamen University.
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Facile regio- and stereoselective hydrometalation of alkynes with a combination of carboxylic acids and group 10 transition metal complexes: selective hydrogenation of alkynes with formic acid.
Ruwei Shen,Tieqiao Chen,Tieqiao Chen,Yalei Zhao,Renhua Qiu,Yongbo Zhou,Shuang-Feng Yin,Xiang-Bo Wang,Midori Goto,Li-Biao Han,Li-Biao Han +10 more
TL;DR: This finding clarifies the long proposed reaction mechanism that operates via the generation of an alkenylpalladium intermediate and subsequent transformation of this complex in a variety of reactions catalyzed by a combination of Brϕnsted acid and Pd(0) complex.
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crystal structures of thiophene/phenylene co-oligomers with different molecular shapes
TL;DR: In this paper, the authors have determined crystallographic structures of four thiophene/phenylene co-oligomers with different molecular shapes, which consist of the molecules straight, bent, or zigzag.
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Stereospecific Coupling of H-Phosphinates and Secondary Phosphine Oxides with Amines and Alcohols: A General Method for the Preparation of Optically Active Organophosphorus Acid Derivatives
TL;DR: This finding leads to the establishment of a general and efficient method for the synthesis of a variety of optically active organophosphorus acid derivatives from the easily available chiral H-phosphinates and secondary phosphine oxides.
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Retention of configuration on the oxidative addition of P-H bond to platinum (0) complexes: the first straightforward synthesis of enantiomerically pure P-chiral alkenylphosphinates via palladium-catalyzed stereospecific hydrophosphinylation of alkynes.
TL;DR: The oxidative addition of pure (R(P)-menthyl phenylphosphinate 1 to a platinum (0) complex proceeds readily with retention of configuration at the chiral phosphorus center, affording high yields of the corresponding vinylphosphinates bearing a single chirality at phosphorus.