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121.
122.
ChristopherW. Cunningham Kellie Hom Chayan Acharya Angela Wilks AlexanderD. MacKerell Andrew Coop 《Helvetica chimica acta》2010,93(2):220-226
The Diels–Alder reaction was applied to 4,5‐epoxymorphinan opioids to generate a novel aromatic cycloadduct at C(7) C(8): Thermolytic cleavage of sultine 8 produced the reactive diene o‐quinodimethane 7 which condensed favorably with codeine ( 11 ), but not with codeinone ( 9 ) or 14‐hydroxycodeinone ( 10 ), producing the desired tetrahydronaphtho adduct 12 with (7R,8R) geometry (Scheme). The configuration of the cycloadduct was determined by 1D‐ and 2D‐NMR experiments. The unanticipated reactivity of these codeine derivatives was investigated by quantum‐mechanical calculations, and it was determined that steric effects of the 6‐keto and 14‐hydroxy group likely precluded condensation by raising the molecular energy of their respective transition states. 相似文献
123.
Abazov VM Abbott B Abolins M Acharya BS Adams M Adams T Agelou M Agram JL Ahn SH Ahsan M Alexeev GD Alkhazov G Alton A Alverson G Alves GA Anastasoaie M Andeen T Anderson S Andrieu B Anzelc MS Arnoud Y Arov M Askew A Asman B Assis Jesus AC Atramentov O Autermann C Avila C Ay C Badaud F Baden A Bagby L Baldin B Bandurin DV Banerjee P Banerjee S Barberis E Bargassa P Baringer P Barnes C Barreto J Bartlett JF Bassler U Bauer D Bean A Begalli M Begel M Belanger-Champagne C Bellantoni L Bellavance A 《Physical review letters》2006,97(15):151804
We present a search for associated Higgs boson production in the process pp-->WH-->WWW*-->l;+/-nul'+/-nu'+X in final states containing two like-sign isolated electrons or muons (e+/-e;+/-, e+/-micro+/-, or micro+/-micro+/-). The search is based on D0 run II data samples corresponding to integrated luminosities of 360-380 pb-1. No excess is observed over the predicted standard model background. We set 95% C.L. upper limits on sigma(pp-->WH)xBr(H-->WW*) between 3.2 and 2.8 pb for Higgs boson masses from 115 to 175 GeV. 相似文献
124.
125.
The scattering of incident plane elastic waves by a varietyof different defects that lie upon a fluid-solid interface isconsidered here using matched asymptotic expansions. The expansionscheme is developed in terms of a parameter , the ratio of typicaldefect length scale to a typical wavelength of the incidentfield, taken to be small. Three different canonical situations occur and these are illustratedvia three specific examples treated here: a rigid strut, anedge crack, and a rigid strip. In each case the leading-ordermatching is performed to identify the leading-order contributionof the defect to the acoustic field in the far field. In particular,each defect is identified with a source of dipole response ininterfacial stress of displacement. It is shown in the limit as s<<s1 that in the inner problemsthe fluid and solid pieces uncouple in a particularly convenientmanner allowing analytical solutions to be deduced. These arethen matched with appropriate outer solutions. 相似文献
126.
Hukum P. Acharya 《Tetrahedron》2006,62(14):3329-3343
Palladium-catalyzed reaction of TBS ether of 4-cyclopentene-1,3-diol monoacetate (>95% ee) with an anion derived from methyl malonate and a base such as t-BuOK and LDA proceeded highly efficiently and reproducibly. The product obtained in >90% isolated yield was transformed in five steps into the key cyclopentenone possessing the α-chain at the γ position. Aldol reaction of this enone with the ω-chain aldehyde afforded the aldol adduct, and exposure of the derived mesylate to Al2O3 furnished the cross-conjugated dienone of the full structure. Finally, functional group manipulation furnished Δ12-PGJ2 efficiently. Similarly, 15-deoxy-Δ12,14-PGJ2, 5,6-acetylene analogues, and a 5,6-dihydro analogue were synthesized. 相似文献
127.
Hukum P. Acharya 《Tetrahedron letters》2005,46(48):8435-8438
Use of the PMBOCH2 group (PMB: p-MeOC6H4CH2) as a substitute of CO2H provided high level of reproducibility and efficiency in construction of the full structure of 5,6-epoxyisoprostane A2. After the construction, the PMBOCH2 group was converted to CO2H by using (1) DDQ, (2) SO3·pyridine and (3) NaClO2 at pH 7. The acid, thus synthesized, was condensed with lyso-PC to furnish one of the title compounds. Similarly, 14,15-regioisomer was synthesized. 相似文献
128.
Hukum P. Acharya 《Tetrahedron letters》2004,45(6):1199-1202
A key cyclopentenone possessing the α-chain was synthesized from TBS ether of 4-cyclopentene-1,3-diol monoacetate, and submitted to aldol reaction at the α′-position with the ω-chain aldehydes followed by dehydration to produce the title compounds. In a similar manner, 5-dehydro compounds (acetylene analogues) were synthesized successfully. In addition, palladium-catalyzed reaction of 4-cyclopentene-1,3-diol monoacetate with methyl malonate, the first step of the synthesis, was improved to afford the product in high yield by using t-BuOK or LDA in place of NaH. 相似文献
129.
Roy M. Choudhary R. N. P. Acharya H. N. 《Journal of Thermal Analysis and Calorimetry》1989,35(5):1471-1476
Dysprosium molybdate, Dy2(MoO4)3, displays a ferroelectric phase transition at 145 °C. The X-ray and thermal (DTA, TG and DSC) properties of this compound have been studied. The X-ray study confirmed the ferroelectric phase in the orthorhombic space group Pba2. Thermal analysis demonstrated the existence of a ferroelectric and another phase transition in this compound.
The authors wish to thank Prof. A. Paul and Mr. R. Bhatnagar for their kind help in some of the experimental work. One of us (MR) gratefully acknowledges a Fellowship from DST, Government of India. 相似文献
Zusammenfassung Dysprosiummolybdat, Dy2(MoO4)3 (Abk.: DMO), ein Vertreter der Seltener-denmolybdatreihe zeigt bei 145 °C einen ferroelektrischen Phasenübergang. Röntgendiffraktion und thermische Eigenschaften (DTA, TG, DSC) der genannten Verbindung wurden untersucht. Auf Grund der Röntgendiffraktionsuntersuchung gehört die ferroelektrische Phase in die orthorhombische Raumgruppe Pba2. Mittels Thermoanalyse konnte bei dieser Verbindung die Existenz ferroelektrischer und anderer Phasenübergänge nachgewiesen werden.
145 °C. (, ) . , Pba2. .
The authors wish to thank Prof. A. Paul and Mr. R. Bhatnagar for their kind help in some of the experimental work. One of us (MR) gratefully acknowledges a Fellowship from DST, Government of India. 相似文献
130.
Ionization of the internucleotidic 2'-hydroxyl group in RNA facilitates transesterification reactions in Group I and II introns (splicing), hammerhead and hairpin ribozymes, self-cleavage in lariat-RNA, and leadzymes and tRNA processing by RNase P RNA, as well as in some RNA cleavage reactions promoted by ribonucleases. Earlier, the pK(a) of 2'-OH in mono- and diribonucleoside (3'-->5') monophosphates had been measured under various nonuniform conditions, which make their comparison difficult. This work overcomes this limitation by measuring the pK(a) values for internucleotidic 2'-OH of eight different diribonucleoside (3'-->5') monophosphates under a set of uniform noninvasive conditions by 1H NMR. Thus the pK(a) is 12.31 (+/-0.02) for ApG and 12.41 (+/-0.04) for ApA, 12.73 (+/-0.04) for GpG and 12.71 (+/-0.08) for GpA, 12.77 (+/-0.03) for CpG and 12.88 (+/-0.02) for CpA, and 12.76 (+/-0.03) for UpG and 12.70 (+/-0.03) for UpA. By comparing the pK(a)s of the respective 2'-OH of monomeric nucleoside 3'-ethyl phosphates with that of internucleotidic 2'-OH in corresponding diribonucleoside (3'-->5') monophosphates, it has been confirmed that the aglycons have no significant effect on the pK(a) values of their 2'-OH under our measurement condition, except for the internucleotidic 2'-OH of 9-adeninyl nucleotide at the 5'-end (ApA and ApG), which is more acidic by 0.3-0.4 pK(a) units. 相似文献