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Akiba Y Beavis D Beery P Britt HC Budick B Chasman C Chen Z Chi CY Chu YY Cianciolo V Cole BA Costales JB Crawford HJ Cumming JB Debbe R Engelage J Fung SY Gonin M Gushue S Hamagaki H Hansen O Hayano RS Hayashi S Homma S Kaneko H Kang J Kaufman S Kehoe WL Kurita K Ledoux RJ Levine MJ Miake Y Morrison DP Morse RJ Moskowitz B Nagamiya S Namboodiri MN Nayak TK Olness J Parsons CG Remsberg LP Roehrich D Rothschild P Sakurai H Sangster TC Seto R Soltz R Stankus P Steadman SG Stephans GS Sung T 《Physical review letters》1996,76(12):2021-2024
44.
Yoshiharu Izumi 《Angewandte Chemie (International ed. in English)》1971,10(12):871-881
It is proposed that asymmetric syntheses be divided into enantioselective and diastereoselective syntheses. The enantioselective hydrogenations discussed in the present progress report were catalyzed by Raney nickel that had previously been treated with solutions of optically active compounds. Relationships exist between the enantioselectivity of the catalyst and the structure of the chiral compound used to modify it. 相似文献
45.
Four possible diastereomers of pentenocin B were synthesized in a stereocontrolled manner, and the first total synthesis of a natural enantiomer of (+)-pentenocin B unequivocally established the absolute stereochemistry to be 4S,5R,6R. 相似文献
46.
Michiko Iwamura Yuka Gotoh Tomoyuki Hashimoto Reiko Sakurai 《Tetrahedron letters》2005,46(37):6275-6277
Michael addition reactions of acetoacetates and malonates with acrylates in a 5 M KOH aqueous solution without using any other catalysts are described. When they are either tert-butyl or benzyl esters, the reaction proceeded very rapidly to afford moderate to high yields of the corresponding bis-Michael adducts that are unexpectedly stable under these conditions. 相似文献
47.
Tominaga Keii Yoshiharu Doi Hiromu Kobayashi 《Journal of polymer science. Part A, Polymer chemistry》1973,11(8):1881-1888
Mass transfer which affects the rate of propylene polymerization with titanium trichloride–triethylaluminum, has been evaluated by use of a new method developed for this heterogeneous reaction. The polymerization was carried out with the usual flask reactor equipped with a paddle stirrer; the rate of gas absorption into the polymerization slurry was proportional to stirring speed and the reciprocal of the total amount of polymers produced. It has been confirmed that the polymerization rate separated from the absorption rate is purely kinetic (propagation), and an effective physical process, such as monomer transfer through a polymer film covering the catalyst surface, no longer exists. 相似文献
48.
Hiroshi Sakurai Akira Tatematsu Hisao Nakata 《Journal of mass spectrometry : JMS》1973,7(9):1109-1110
A novel rearrangement reaction for a methyl group is found in doubly charged ion mass spectra of p-substituted acetophenone derivatives. The driving force for the reaction is discussed. 相似文献
49.
Nevin Çelebi Osamu Shirakura Yoshiharu Machida Tsuneji Nagai 《Journal of inclusion phenomena and macrocyclic chemistry》1987,5(4):407-413
Inclusion complex formation of piromidic acid (PA) with dimethyl--cyclodextrin (DM--CD) in aqueous solution and in the solid state was confirmed by the solubility method, differential scanning calorimetry (DSC) and proton nuclear magnetic resonance (1H-NMR) spectroscopy. The apparent stability constant,K
c
, of the complex was estimated to be 244 M–1. The stoichiometry of the complex was given as the ratio 1:2 of PA to DM--CD. The dissolution rate of the PA/DM--CD complex was much greater than that of intact PA.Presented at the Fourth International Symposium on Inclusion Phenomena and the Third International Symposium on Cyclodextrins, Lancaster, U.K., 20–25 July 1986. 相似文献
50.