Motoki Yamane

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Organization: Nanyang Technological University , Singapore
Department: School of Physical and Mathematical Sciences
Title: (PhD)

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Co-reporter:Chuan Zhu;Chao Feng
Chemical Communications 2017 vol. 53(Issue 17) pp:2606-2609
Publication Date(Web):2017/02/23
DOI:10.1039/C7CC00562H
An efficient synthesis of (3-isoindazolyl)allenes from 2-alkynyl azobenzenes and terminal alkynes via cooperative Pd(PPh3)2Cl2/CuI-catalyzed cross-coupling has been developed. By making use of this approach, (3-isoindazolyl)allenes with various substituents can be synthesized in good to excellent yields. A rapid synthesis of biologically active indazolo[2,3-a]quinoline was also achieved using this method as the key step.
Co-reporter:Chuan Zhu and Motoki Yamane
Organic Letters 2012 Volume 14(Issue 17) pp:4560-4563
Publication Date(Web):August 17, 2012
DOI:10.1021/ol302024m
A practical and simple method for deaminoborylation of aryltriazene with bis(pinacolato)diboron has been developed that is mediated by BF3·OEt2. Various arylboronic esters are prepared in moderate to good yields with this facile transition-metal-free procedure.
Co-reporter:Chuan Zhu, Noriaki Yukimura and Motoki Yamane
Organometallics 2010 Volume 29(Issue 9) pp:2098-2103
Publication Date(Web):April 9, 2010
DOI:10.1021/om100067r
Oxygen-bridged and sulfur-bridged rhodium homobimetallic complexes were synthesized as air-stable crystals by using 2,6-bis(phosphanylmethyl)phenolate and -thiophenolate as the ligands, respectively. The oxygen-bridged dirhodium complex has a symmetrical structure where the carbon atom at the ipso position, oxygen, and two rhodium atoms are located in the same plane. It is thermally stable compared to the sulfur-bridged dirhodium complex and shows catalytic activity for hydrogenation of alkenes with high chemoselectivity.
Co-reporter:Chuan Zhu, Chao Feng and Motoki Yamane
Chemical Communications 2017 - vol. 53(Issue 17) pp:NaN2609-2609
Publication Date(Web):2017/02/03
DOI:10.1039/C7CC00562H
An efficient synthesis of (3-isoindazolyl)allenes from 2-alkynyl azobenzenes and terminal alkynes via cooperative Pd(PPh3)2Cl2/CuI-catalyzed cross-coupling has been developed. By making use of this approach, (3-isoindazolyl)allenes with various substituents can be synthesized in good to excellent yields. A rapid synthesis of biologically active indazolo[2,3-a]quinoline was also achieved using this method as the key step.
1-Buten-1-ol, 4-phenyl-1-(trimethylsilyl)-, benzoate, (1E)-
Benzamide, 3-methoxy-N-(phenylmethyl)-
2-Butenoic acid, 4-oxo-4-[(phenylmethyl)amino]-, ethyl ester, (2E)-
Pyrrolidine, 1-[(4-fluorophenyl)azo]-
ETHENOL, 2-PHENYL-1-(TRIMETHYLSILYL)-, BENZOATE, (1E)-
Carbonic acid, phenylmethyl propyl ester
Pyrrolidine, 1-[(4-methoxyphenyl)azo]-
Ethanone, 1,1'-(1,2-ethynediyldi-4,1-phenylene)bis-
Pyrrolidine, 1-[(2-methylphenyl)azo]-
2,2'-Bibenzofuran