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Chiral hydrocarbon [2.2]paracyclophanes act as chiral initiators in asymmetric autocatalysis in the addition of diisopropylzinc to pyrimidine-5-carbaldehyde and give highly enantiomerically enriched 5-pyrimidyl alkanol with a reversed sense of the enantioselectivity to that of other [2.2]paracyclophanes with heteroatoms. 相似文献
95.
Takaguchi Y Tajima T Yanagimoto Y Tsuboi S Ohta K Motoyoshiya J Aoyama H 《Organic letters》2003,5(10):1677-1679
[reaction: see text] Thermotropic liquid crystallinity can be induced for an anthracene having a dendritic substituent. The photodimerization reaction of an anthracene moiety in the smectic phase proceeded quantitatively and regioselectively. 相似文献
96.
We developed a compact three-stage Ti:sapphire amplifier laser system that produced peak power in excess of 100 TW for a pulse duration of less than 19 fs and an average power of 19 W at a 10-Hz repetition rate. A final 40-mm-diameter Ti:sapphire amplifier is pumped by a Nd:YAG master-oscillator-power-amplifier system that produces ~7-J output of 532-nm radiation. The spatial beam quality is approximately 2 times diffraction limited for the full amplified compressed output pulse. With f/3 optics, this system should therefore be capable of producing a focused intensity of ~3x10(20) W/cm(2) . 相似文献
97.
Homologation of ketones can be achieved with trimethylsilyldiazomethane(TMSCHN2) which is a stable and safe substitute for hazardous diazomethane. 相似文献
98.
Yoichi Aoyama 《manuscripta mathematica》1977,22(3):225-228
Let k be a perfect field and S the quotient ring of a polynomial ring k[X1,...,Xt] with respect to a prime ideal. Let I be a prime ideal of S such that R=S/I is an almost complete intersection. Then, in his paper [2], Matsuoka proves that the homological dimension of the differential module R/Kis infinite under the assumption that R is Cohen-Macaulay and I2 is a primary idea]. In this paper we prove that the result is valid without the above assumption. 相似文献
99.
Hosoya T Hiramatsu T Ikemoto T Nakanishi M Aoyama H Hosoya A Iwata T Maruyama K Endo M Suzuki M 《Organic & biomolecular chemistry》2004,2(5):637-641
A novel method for radioisotope-free photoaffinity labeling was developed, in which a bifunctional ligand is connected to a target protein by activation of a photoreactive group, such as an aromatic azido or 3-trifluoromethyl-3H-diazirin-3-yl group, and identification of the ligated product is achieved by anchoring of a detectable tag through the Staudinger-Bertozzi reaction with an alkyl azido moiety that survives photolysis. The chemical ground of this method was confirmed using model compounds with the bifunctional group under photoirradiation in the presence of trapping agents for reactive intermediates. The utility of the method has been demonstrated by specific labeling of the catalytic portion of human HMG-CoA reductase. 相似文献
100.
A convenient method for the synthesis of mono- and N,N-disubstituted thioureas by the debenzoylation of N-substituted- and N,N-disubstituted-N′-benzoylthioureas with hydrazine hydrate under solvent-free conditions has been developed. N-Substituted-N′-benzoylthioureas and hydrazine hydrate were mixed, and stirred at room temperature without a solvent to give the corresponding N-substituted thioureas in high yields. 相似文献