Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Hayao Matsuhashi"'
Autor:
Hayao Matsuhashi, Qiaogong Su
Publikováno v:
Organic Process Research & Development. 25:627-631
Unexpected failures of a Heck reaction in the lab led to the detection of 5-hydroperoxy-1-methyl-2-pyrrolidinone (NMP-5-OOH) in the cosolvent 1-methyl-2-pyrrolidinone (NMP). This hydroperoxide, for...
Autor:
David E. White, Frederick G. Vogt, Lianming Wu, Connie Ye, Gerald J. Terfloth, Hayao Matsuhashi
Publikováno v:
Journal of Mass Spectrometry. 47:836-844
While the occurrence of desulfurization of phosphorothioate oligonucleotides in solution is well established, this study represents the first attempt to investigate the basis of the unexpected desulfurization via the net sulfur-by-oxygen (S-O) replac
Autor:
Richard M. Goodman, Hao Yin, Susan V. Downing, Alan Joseph Hennessy, Eric A. Voight, Jeffery L. Wood, Stacie Calad, Hayao Matsuhashi, Ilaria Giordano
Publikováno v:
Organic Letters. 12:3422-3425
An efficient enantioselective total synthesis of the potent antibiotic GSK966587 was accomplished. Highlights of the synthesis include two innovative Heck reactions, a highly selective zincate base directed ortho-metalation, Sharpless asymmetric epox
Autor:
William M. Clark, Huan Wang, Doan Brian Daniel, Xi Ouyang, Hayao Matsuhashi, Steven N. Goodman
Publikováno v:
Tetrahedron. 65:6291-6303
Two stereoselective syntheses of SB-462795, a highly potent cathepsin K inhibitor, are described. Both routes feature a C5–C6 disconnection by ring closing metathesis to construct an azepane ring and are amenable to large-scale manufacturing.
Autor:
Hayao Matsuhashi, Kousei Shimada
Publikováno v:
Tetrahedron. 58:5619-5626
Chemical transformation of Leustroducsin H to Leustroducsin B has been successfully accomplished in 11 steps including enzymatic hydrolysis of phosphate ester. The process described here enables to differentiate all hydroxyl groups, amino and phospha
Autor:
Tamejiro Hiyama, Kazunori Hirabayashi, Atsunori Mori, Masaki Shimizu, Hayao Matsuhashi, Akinori Fujita, Makoto Tanaka
Publikováno v:
Organometallics. 15:5762-5765
Palladium-catalyzed cross-coupling reaction of optically active (2-cyclohexenyl)difluorophenylsilane with 4-iodoacetophenone in the presence of tetrabutylammonium fluoride furnishes the corresponding cross-coupled product with retention of the stereo
Autor:
Manabu Kuroboshi, Hayao Matsuhashi, Hideaki Ohmura, Ken-ichi Goda, Yasuo Hatanaka, Makoto Tanaka, Tamejiro Hiyama
Publikováno v:
Journal of Organometallic Chemistry. 499:167-171
A palladium complex with an optically active ligand catalyzes asymmetric hydrosilylation of 1,3-dienes using difluoro(phenyl)silane to give optically active allyl difluoro(phenyl)silanes in good enantiomeric excess.
Autor:
Lianming, Wu, David E, White, Connie, Ye, Frederick G, Vogt, Gerald J, Terfloth, Hayao, Matsuhashi
Publikováno v:
Journal of mass spectrometry : JMS. 47(7)
While the occurrence of desulfurization of phosphorothioate oligonucleotides in solution is well established, this study represents the first attempt to investigate the basis of the unexpected desulfurization via the net sulfur-by-oxygen (S-O) replac
Publikováno v:
Tetrahedron Letters. 35:6507-6510
A variety of alkyltrifluorosilanes were found to couple with aryl halides in the presence of Pd(PPh3)4 catalyst and tetrabutylammonium fluoride (TBAF) to give the corresponding cross-coupled products in moderate to good yields.
Publikováno v:
ChemInform. 26
A variety of alkyltrifluorosilanes were found to couple with aryl halides in the presence of Pd(PPh3)4 catalyst and tetrabutylammonium fluoride (TBAF) to give the corresponding cross-coupled products in moderate to good yields.