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1.
Following a bonding reaction with octadecyldimethyl-N,N-diethylaminosilane (ODS-DEA), a monolithic silica was subjected to consequential on-line endcapping reactions with hexamethyldisilazane (HMDS) or N-(trimethylsilyl)imidazole (TMSI) to compare the two reagents. Endcapping of monolithic silica C(18) columns prepared by a manufacturer was also studied. After endcapping with TMSI in acetonitrile (ACN), all columns provided better performance for hydrogen-bonding compounds and basic compounds than C(18) phases endcapped with HMDS. TMSI endcapping of commercial Chromolith Performance columns also gave improved performance. The results indicate that one can significantly improve the performance of monolithic silica C(18) columns for basic compounds by a simple on-column reaction with TMSI in ACN at a relative low temperature. 相似文献
2.
The group transfer polymerization (GTP) of n-butyl acrylate (nBuA) using 1-methoxy-1-(trimethylsiloxy)-2-methyl-1-propene (MTS) as an initiator, mercuric iodide (HgI2) as a catalyst in toluene at room temperature gives a very good control of molecular weight and narrow molecular weight distribution. (M̄w/M̄n < 1.2). Kinetic studies in this system reveal that this reaction is rather slow, half-lives being in the range of hours. The kinetic order of the apparent rate constant of propagation with respect to initiator and catalyst concentrations were found to be near to unity. However, the first-order time-conversion plots exhibit considerable induction periods. Upon addition of trimethylsilyl iodide (TMSI) the induction periods vanish and the rates are increased by two orders of magnitude. The reaction is first-order with respect to TMSI indicating that it takes part in the reaction by activating the catalyst. The complex from HgI2 and TMSI acts as a nucleophilic catalyst, similar to oxyanions in the GTP of MMA in THF. It is proposed that the induction periods are due to the formation of TMSI from MTS and HgI2. 相似文献
3.
Kyung Hoi Cha Tae Won Kang Hong-Woo Lee Eung-Nam Kim Nam-Hee Choi Jung-Woo Kim 《合成通讯》2013,43(12):2131-2136
Triphenylphosphine (TPP)-iodotrimethylsilane (TMSI) was found to be a convenient and highly effective catalyst for the tetrahydropyranylation of aliphatic and aromatic alcohols with dihydropyran in dichloromethane at ambient temperature. 相似文献
4.
The reactivity of the double-stranded hydrocarbon cycle with two ether bridges (1) toward iodotrimethylsilane (TMSI) was investigated in some detail. The carbon skeleton of cycle 1 resembles the belt region of a C84 fullerene which makes it a potential precursor to the long sought after fully aromatic derivative. Upon exposure to TMSI, cycle 1 undergoes a cascade of reactions which involve different states of iodination/reduction which ultimately lead to the hydrogenated cycle 5a, whose structure was proven by single-crystal X-ray analysis. A deeper insight into mechanistic aspects of this sequence of conversions was gained by performing the reaction under dry and wet conditions, whereby the latter involved both normal and deuterated water. With the help of detailed NMR correlation studies and DFT computations, all important aspects were clarified including an unexpected selective H/D exchange at the naphthalenic moieties. 相似文献
5.
A new, convenient and good yield reduction of cephalosporin S (β)-sulphoxides to the corresponding sulphides was achieved upon treatment with iodotrimethylsilane (TMSI) in dichloromethane. 相似文献
6.
Stereoselective conjugate additions to chiral N-enoyl amides employing various monoorganocuprate reagents, Li[RCuI], are described. The presence of TMSI in the addition of Li[RCuI] in THF provided the highest stereoselectivities. Reversed major diastereomeric ratios were obtained employing Li[RCuI] in ether or conventional copper-promoted Grignard reagents. The results presented support the favored anti-s-cis conformation of the substrates using Li[RCuI]/TMSI in THF, while the copper-promoted Grignard reagents or the Li[RCuI] reagents in ether favor the opposite syn-s-cis conformation. Influence of lithium ions on the stereoselective conjugate addition of the monoorganocuprate reagent, Li[BuCuI], has been investigated and two different mechanistic pathways are presented. The results show that iodotrimethylsilane (TMSI) is crucial for the asymmetric conjugate addition of the copper reagent, but only in THF or when 12-crown-4 is used. The reaction is thought not to involve any halosilane in any critical steps in the organocopper mechanisms conducted in ether. The (CuI)4(SMe2)3 complex precursor plays an instrumental role for the conjugate addition using monoorganocopper reagents. 相似文献
7.
Kyung Hoi Cha Tae Won Kang Dong Ock Cho Hong-Woo Lee Jaewook Shin Kyung Yong Jin 《合成通讯》2013,43(20):3533-3540
Diphenylmethyl (DPM) and p-methoxybenzyl (PMB) ester of cephalosporin derivatives were converted to the corresponding carboxylic acid using iodotrimethylsilane (TMSI)-triphenylphosphine (TPP) in dichloromethane at room temperature in good yields. 相似文献
8.
Christopher M. Bates Marco A. Bedolla Pantoja Jeffrey R. Strahan Leon M. Dean Brennen K. Mueller Christopher J. Ellison Paul F. Nealey C. Grant Willson 《Journal of polymer science. Part A, Polymer chemistry》2013,51(2):290-297
The successful synthesis, characterization, and directed self‐assembly of a silicon‐containing block copolymer, poly(styrene‐block‐trimethylsilylisoprene) (P(S‐b‐TMSI)), which has much higher oxygen etch contrast than the de facto standard, poly(styrene‐block‐methyl methacrylate) is reported. A Sakurai, Grignard‐type coupling reaction provided the key monomer in good yield. Living anionic polymerization was employed to prepare the block copolymer, which has very low polydispersity. P(S‐b‐TMSI) was successfully ordered and oriented by directed self‐assembly. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
9.
The direct synthesis of 3-iodomethyl cephalosporin esters from 3-acetoxy- and 3-carbamoylmethyl analogues may be achieved using TMSI. The “one-pot” conversion of sodium cephalothin into a C-3 heterocycle-substituted cephalosporin may also be performed using TMSI-mediated chemistry. 相似文献
10.
Abed Badrian Manouchehr Mamaghani Sharif Kaamyabi 《Phosphorus, sulfur, and silicon and the related elements》2016,191(10):1375-1379
Trimethylsilyl iodide (TMSI) is introduced as an efficient reagent for the one-pot and direct transformation of carbamates of unsaturated β-aminoesters into the corresponding α-methylene-β-lactams and α-arylidene-β-lactams. The mild reaction conditions, excellent yields and easy work-up procedures make it a useful alternative to previously applied procedures for the rapid synthesis of β-lactams from easily available Baylis-Hillman adducts. 相似文献
11.
Isao Kadota Yuji Yamagami Naoya Fujita Hiroyoshi Takamura 《Tetrahedron letters》2009,50(31):4552-4553
A useful method for the selective cleavage of primary MPM ethers by using TMSI/Et3N is described. Other protective groups such as secondary MPM ethers, silyl ethers, and benzylidene acetal were stable under the reaction conditions. 相似文献
12.
16Alpha-hydroxy-17-keto steroids, 1, 3, and 8, and their 17beta-hydroxy-16-keto isomers, 4, 5, and 9, were transformed into the corresponding 17beta-alkoxy-16-keto derivatives on treatment with trimethylsilyl iodide (TMSI) in the presence of alkyl alcohol in CHCl3 in poor to high yields. 相似文献
13.
Gowravaram Sabitha G.S.Kiran Kumar ReddyCh.Srinivas Reddy J.S. Yadav 《Tetrahedron letters》2003,44(21):4129-4131
The synthesis of various substituted Hantzsch 1,4-dihydropyridines has been achieved using the classical Hantzsch procedure and modified Hantzsch conditions for the first time at room temperature in the presence of iodotrimethylsilane (TMSI) generated in situ in CH3CN, in excellent yields. 相似文献
14.
Gowravaram Sabitha K. Bhaskar Reddy M. Bhikshapathi J.S. Yadav 《Tetrahedron letters》2006,47(16):2807-2810
The Prins-type cyclization of ketones with homoallylic and homopropargylic alcohols in the presence of TMSI generated in situ from TMSCl and NaI produced 2,2-disubstituted- or spirocyclic-4-iodo-tetrahydropyrans and spirocyclic-4-iodo-5,6-dihydro-2H-pyrans in good yields. These iodopyrans are reported for the first time. 相似文献
15.
An efficient method for mono-phosphorylation of 2(KRP203)using cbz-protection,dibenzylphosphoryl chloride and TMSI affording 2-P(KRP203-P)was developed.We applied the present method to the synthesis of KRP203 phosphate analogs which were difficult to produce through tradition procedures. 相似文献
16.
A Iwado M Mifune Y Mori M Onoda T Kanai N Motohashi J Haginaka Y Saito 《Analytical sciences》2001,17(2):301-305
As an attempt to elucidate the factor(s) responsible for the poor performance of a copper(II)-phthalocyanine aminopropylsilica gels (CU-PCSD) column for HPLC, the silanol and/or amino groups remaining on Cu-PCSD were endcapped with trimethylchlorosilane (TMCS) or N-trimethylsilylimidazole (TMSI). The trimethylsilylated Cu-PCS(D)S (Cu-PCSD-TMCS and -TMSI) were investigated concerning their performance as an HPLC-stationary phase in the separation of pi-electron-rich polyaromatic hydrocarbons (PAHs), such as mutagenic anthracene and pyrene. As a result, trimethylsilylation with TMSI, which reacts only with silanol-groups, was not effective to improve the column efficiency. In contrast, trimethylsilylation by TMCS, which reacts with both the silanol- and amino-groups, improved the theoretical plate numbers (N) for PAHs separation with the Cu-PCS(D) column, indicating that the low N values on the Cu-PCSD column were caused by electrostatic interactions between PAHs and the remaining amino-groups on Cu-PCS(D). Furthermore, the retention data of mutagenic heterocyclic amines (HCAs) indicated that the remaining amino groups interact with the polar groups of HCAs. 相似文献
17.
V. Seidel B. Lang S. Fraißler C. Lang K. Schiller G. Filek W. Lindner 《Chromatographia》1993,37(3-4):191-201
Summary Various analytical methods developed for trichothecene determination, including TLC, HPLC, GC, supercritical fluid chromatography (SFC) and enzyme immuno assay (EIA) are reviewed. In addition a new method is described for the simultaneous determination of the trichothecene mycotoxins deoxynivalenol (DON), nivalenol (NIV), 3-acetyldeoxynivalenol (3-ADON), diacetoxyscirpenol (DAS), T-2 toxin (T-2), HT-2 toxin (HT-2) and T-2 triol (TRIOL), in Austrian wheat and corn samples by GC-ECD. A clean-up procedure has been developed using a combination of liquid-liquid and liquid-solid extraction. Trichothecenes were detected as their heptafluorobuturyl esters or alternatively as trimethylsilyl ethers (only sensitive for deoxynivalenol and nivalenol) using nandrolone or chloramphenicol as internal standard. Four derivatization techniques using HFBI, HFBA+DMAP on polystyrene, TMSI and TMSI+BSA+TMCS have been studied and the advantages and disadvantages of each are discussed. Quantification of trichothecenes from 10 to 1000 ppb in cereals could be accomplished routinely.Presented at the 19th ISC, Aix-en-Provence, France, September 13–18, 1992. 相似文献
18.
Luisa Köhler Dr. Michael Patzschke Dr. Stephen Bauters Dr. Tonya Vitova Dr. Sergei M. Butorin Prof. Dr. Kristina O. Kvashnina Dr. Moritz Schmidt Prof. Dr. Thorsten Stumpf Dr. Juliane März 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(21):e202200119
Reaction of the N-heterocylic carbene ligand iPrIm (L1) and lithium bis(trimethylsilyl)amide (TMSA) as a base with UCl4 resulted in U(IV) and U(V) complexes. Uranium's +V oxidation state in (HL1)2[U(V)(TMSI)Cl5] (TMSI=trimethylsilylimido) ( 2 ) was confirmed by HERFD-XANES measurements. Solid state characterization by SC-XRD and geometry optimisation of [U(IV)(L1)2(TMSA)Cl3] ( 1 ) indicated a silylamido ligand mediated inverse trans influence (ITI). The ITI was examined regarding different metal oxidation states and was compared to transition metal analogues by theoretical calculations. 相似文献
19.
[reaction: see text] The influence of lithium ions on the conjugate addition of the monoorganocuprate reagent, Li[BuCuI], to a chiral crotonate has been investigated. The results show that iodotrimethylsilane (TMSI) is crucial for the asymmetric conjugate addition of the copper reagent, but only in THF or when 12-crown-4 is used. The reaction is thought not to involve any halosilane in any critical steps in the organocopper mechanisms conducted in Et(2)O. 相似文献
20.
The study showed that a combination of an achiral silicon-based Lewis acid and chiral Lewis base, such as iodotrimethylsilane (TMSI) and cinchonine, generated a highly enantioselective catalyst system under solvent-free conditions which gave aromatic β-amino ketones with up to >99% ee. Mechanistic studies demonstrate the enhanced asymmetric induction may be due to the combined and competitive activation of a carbonyl moiety of chalcone with cinchonine and the silicon-based Lewis acid in the aza-Michael reaction. 相似文献