Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Michinori Ōki"'
Publikováno v:
Heteroatom Chemistry. 15:241-245
The title organoboron complex undergoes dissociation of the intramolecular B–S coordination bond much faster than the corresponding mono ethylthiomethyl complex as revealed by the dynamic NMR study. The facile dissociation is attributable to an SN2
Publikováno v:
Tetrahedron. 58:10345-10351
All the three possible rotamers of the title compound were separated by chromatography, and unambiguously identified by NMR and X-ray analysis. One of the isomers was optically inactive Ci conformation. The other optical active forms were resolved to
Autor:
Michinori Oki
Rotation about the Carbon-Carbon single bond is generally regarded to be unrestricted. About 50 years ago, rotational isomers were found to exhibit optical activity: substituted biphenyl derivatives. However, the author has investigated other classes
Publikováno v:
Tetrahedron Letters. 39:7729-7732
2-Fluoro-4,4,5,5-tetramethyl-1,3-dioxolane was shown to be a useful compound for independently determining the rate constants of contact ion pair and solvent-separated ion pair formations. The compound was used to determine rate constants for toluene
Publikováno v:
Organometallics. 17:4155-4163
To distinguish between dissociation of a B−N coordination bond by SN1- and SN2-type mechanisms, two series of 1,3,2-dioxaborolanes (boronates) and BEt2 (borane) complexes carrying a 2,6-bis((dimeth...
Publikováno v:
Organometallics. 16:4012-4015
Mono-, bis-, and tris(tricarbonylchromium) complexes of triptycene were synthesized by the reaction of triptycene with Cr(CO)6. The stereochemistry of the two isomeric bimetallic complexes of Cs and C2v symmetries was determined from the NMR spectra.
Publikováno v:
Tetrahedron Letters. 38:4575-4578
Reactions of ap- and sp-rotamers of 1-(9-fluorenyl)-2-(1-methylethenyl)-naphthalene with m-chloroperoxybenzoic acid afforded the corresponding epoxides. Of these, the ap-epoxide was found to contain a carbon atom, the structure of which is a distorte
Autor:
Michinori Ōki, Shinji Toyota
Publikováno v:
Journal of Organometallic Chemistry. 534:1-6
An unusually stable organocopper compound carrying an intramolecular sulfane ligand, 2-(ethylthio)phenylcopper, was synthesized via the reaction of the corresponding organolithium with a copper(I) halide (CuX). This compound was obtained in two forms
Publikováno v:
Heteroatom Chemistry. 8:35-43
The mechanism of isomerization of allyl thiocyanate to allyl isothiocyanate has been investigated both experimentally and theoretically. The kinetic study indicates that the reaction is unimolecular and is not ionic. The entropy of activation suggest
Publikováno v:
Journal of the American Chemical Society. 118:11460-11466
Optically active and inactive rotational isomers of 9-(1,1-dimethyl-3-butenyl)-11,12-bis(methoxycarbonyl)-9,10-dihydro-9,10-ethenoanthracene were isolated. The absolute conformations of these optic...