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1.
K. C. Kumara Swamy E. Balaraman M. Phani Pavan N. N. Bhuvan Kumar K. Praveen Kumar N. Satish Kumar 《Journal of Chemical Sciences》2006,118(6):495-501
The diversity of products in the reaction of diethyl azodicarboxylate (DEAD)/diisopropyl azodicarboxylate (DIAD) and activated
acetylenes with PIII compounds bearing oxygen or nitrogen substituents is discussed. New findings that are useful in understanding the nature
of intermediates involved in the Mitsunobu reaction are highlighted. X-ray structures of two new compounds (2-t-Bu-4-MeC6H3O)P (μ-N-t-Bu)2P+[(NH-t-Bu)N[(CO2]-i-Pr)(HNCO2-i-Pr)]](Cl-)(2-t-Bu-4-MeC6H3OH)(23)and [CH2(6-t-Bu-4-Me-C6H2O)2P(O)C(CO2Me)C-(CO2Me)CClNC(O)Cl] (33) are also reported. The structure of23 is close to one of the intermediates proposed in the Mitsunobu reaction. 相似文献
2.
Sajid Husain Ponnapalli Nageswara Sarma Sankarayya Swamy 《Journal of separation science》1995,18(7):422-424
A capillary GC method employing an internal standard has been developed and successfully used for quantitative determination both of the raw materials used for the manufacture of m-phenoxybenzaldehyde and for the components of the reaction mixtures obtained at various stages of the development of the process. A complete analysis can be performed in a single temperature programmed run. 相似文献
3.
The perovskite La2MnZnO6 has been synthesized by a ceramic technique and its catalytic activity has been tested for 2-propanol decomposition. The catalyst is totally selective to dehydrogenation of the alcohol. A possible mechanism for the reaction is proposed.
La2MnZnO6 2-. . .相似文献
4.
Reddy PN Srikanth R Swamy NS Srinivas R Sharma GV Nagendar P Krishna PR 《Journal of mass spectrometry : JMS》2005,40(11):1429-1438
Positive and negative ion electrospray ionization (ESI) tandem mass spectral study of a new series of hybrid peptides, viz, BocN-alpha,beta-peptides and BocN-beta,alpha-peptides, synthesized from C-linked carbo-beta3-amino acids [Caa (S)] and L-Ala has been carried out. The alpha,beta-peptides have been differentiated from beta,alpha-peptides by the collision-induced dissociation (CID) of [M + H]+ and [M - H]- ions in positive and negative ion ESI-MS respectively. The fragment ion [M + H - C(CH3)3 + H]+ formed from [M + H]+ ions by the loss of 2-methyl-prop-2-ene in alpha,beta-peptides with L-Ala at the N-terminus is insignificant or totally absent for beta,alpha-peptides which have the Caa (S) at N-terminus. The fragment ion [M - H-C(CH3)3OH - HNCO]- formed from [M - H]- of beta,alpha-peptide acids is totally absent for alpha,beta-peptide acids. This has been attributed to the absence of the beta-methylene group in alpha,beta-peptides, and the participation of the beta-methylene group in the loss of HNCO in beta,alpha-peptide acids is confirmed by the deuteration experiments. The CID of [M + H-Boc + H]+ ions of these peptides also produce characteristic fragmentation. In the CID spectra of alpha,beta-peptides, the b(n)+ ions and the resulting y(n)+ ions occur at a mass difference of 243 and 71 Da corresponding to the successive losses of Caa and L-Ala, whereas a mass difference of 71 and 243 Da is observed for beta,alpha-peptides. In contrast to the CID of protonated peptides, the CID of [M - H]- ions of the alpha,beta- and beta,alpha-peptide acids do not give b(n)- ions and show abundant z(n) (-) ions. Further, a pair of diastereomeric dipeptide esters and acids have been distinguished by the CID of [M + H]+ ions. The loss of 2-methyl-prop-2-ene is more pronounced for Boc-NH-Caa(R)-D-Ala-OCH3 (21) and Boc-NH-Caa(R)-D-Ala-OH (23) with Caa (R) at the N-terminus, whereas it is totally absent for Boc-NH-Caa (S)-D-Ala-OCH3 (22) and Boc-NH-Caa(S)-D-Ala-OH (24) peptides, which have Caa (S) at the N-terminus. Thus, on the basis of our previous and present studies, we propose that the CID of [M + H]+ ions provides a simple and useful method for distinguishing the configuration of Caa (S or R) at the N-terminus of BocN-carbo beta,alpha- and beta,beta-dipeptides. 相似文献
5.
Decomposition of N2O has been studied on pure La2CuO4, La2CuO4 with 5 and 10 wt. % LaNi5 and oxidized LaNi5 in the temperature range of 240–490 °C at 50 and 200 Torr initial pressures of N2O. The addition of LaNi5 decreases the energy of activation compared to that of La2CuO4 which has been explained based on the dispersity of NiO over La2CuO4.
N2O La2CuO4 La2CuO4 LaNi5 5–10 .%, 240–490°C N2O 50 200 . LaNi5 , . NiO La2CuO4.相似文献
6.
Catalytic decomposition of N2O has been studied over a series of solid solution La2CuxZn1–xO4 (02O, in the temperature range 330–490°C. The observed trends in the kinetics have been explained based on polaron hopping mechanism. Parallel variation between activity and magnetic susceptibility has been observed.
N2O La2CuxZn1–xO4 (0相似文献2O 200 330–490°C. . .
7.
Decomposition of N2O has been studied over La2Cu0.5M0.5O4 (M=Co, Ni, Cu and Zn) between 380 and 485°C at 50 torr initial pressure of N2O to understand the mutual interaction of two different active metal ions of the same concentration and valence in deciding the physico-chemical and catalytic properties. A multicenter type of adsorption of N2O has been visualized and it is found that the rate is governed by the electronic factor.
N2O La2Cu0,5M0,5O4 (M=Co, Ni, Cu Zn) 380–485°C N2O, 50 . , - . N2O. .相似文献
8.
Kumaraswamy S Kommana P Kumar NS Swamy KC 《Chemical communications (Cambridge, England)》2002,(1):40-41
New modes of 1,3-dipolar cycloaddition are uncovered by the isolation of [CH2(6-t-Bu-4-Me-C6H2O)2]P(C(CO2Me)C(CO2Me)N[NP(N3)(OC6H2-6-t-Bu-4-Me)2CH2]N) (3) and [CH2(6-t-Bu-4-Me-C6H2O)2]P(C(CO2Me)C(CO2Me)C(O)N) (4) on treating [CH2(6-t-Bu-4-Me-C6H2O)2]P-X [X = N3 (1) and NCO (2)] with the dipolarophile MeO2CC identical to CCO2Me; compound 4 undergoes an unprecedented ring expansion upon addition of 2-(methylamino)ethanol to afford the spirocycle [CH2(6-t-Bu-4-Me-C6H2O)2]P(OCH2CH2N(Me)CH(CO2Me)CH(CO2Me)C(O)N) (5). 相似文献
9.
K. J. Tony V. Mahadevan J. Rajaram C. S. Swamy 《Reaction Kinetics and Catalysis Letters》1997,62(1):105-116
Thetrans-dioxo ruthenium (VI) complex, [P(C6H5)3C6H5CH2]+[Ru(O)2OAcCl2] or tetrapropylammonium perruthenate catalyzes the oxidation of secondary alcohols to ketones byN-methylmorpholine-N-oxide (NMO). Kinetic studies showed the formation of a complex between catalyst and substrate (alcohol) as the first step
in the mechanism. 相似文献
10.