about
A simple and convenient one-pot synthesis of substituted isoindolin-1-ones via lithiation, substitution and cyclization of N'-benzyl-N,N-dimethylureas.Crystal structure of 2-(1-methyl-eth-yl)-1,3-thia-zolo[4,5-b]pyridine.Crystal structure of 2-(2-methyl-phen-yl)-1,3-thia-zolo[4,5-b]pyridine.3-Chloro-1-lithiopropene, a functional organolithium reagent, and its reactions with alkylboronates to give 3-alkylprop-1-en-3-ols.Crystal structure of 3-amino-2-propyl-quinazolin-4(3H)-one.Crystal structure of 2,2-dimethyl-N-(5-methyl-pyridin-2-yl)propanamide.Crystal structure of 3-amino-2-ethyl-quinazolin-4(3H)-one.One-pot synthesis of substituted isoindolin-1-ones via lithiation and substitution of N'-benzyl-N,N-dimethylureas.Crystal structure of 2-(3-nitro-phen-yl)-1,3-thia-zolo[4,5-b]pyridine.Crystal structure of 2-cyclo-hexyl-1,3-thia-zolo[4,5-b]pyridine.Asymmetric epoxidation using a singly-bound supported Katsuki-type (salen)Mn complex.Study of regioselective dialkylation of naphthalene in the presence of reusable zeolite catalysts.Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a solvent-free system. Scope of the reaction for substituted ethers.Acylation of aromatic ethers over solid acid catalysts: scope of the reaction with more complex acylating agents.A convenient procedure for bismuth-mediated Barbier-type allylation of aldehydes in water containing fluoride ions.Study of regioselective methanesulfonylation of simple aromatics with methanesulfonic anhydride in the presence of zeolite catalysts.Simultaneous quantification of multiple nucleic acid targets using chemiluminescent probes.An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations.A novel supported Katsuki-type (salen)Mn complex for asymmetric epoxidation.Development and application of a novel acridinium ester for use as a chemiluminescent emitter in nucleic acid hybridisation assays using chemiluminescence quenching.Quantitative analysis of gene expression changes in response to genotoxic compounds.Factors affecting migration of tertiary alkyl groups in reactions of alkylboronic esters with bromomethyllithium.Variation in the site of lithiation of 2-(2-methylphenyl)ethanamine derivatives.Highly selective 5-substitution of 3-methylthiophene via directed lithiation.Lithiation of 2-Alkyl-3-amino- and 2-Alkyl-3-(methylamino)-4(3H)-quinazolinones(1).Toxicity and DNA damage induced by 1-nitropyrene and its derivatives in Chinese hamster lung fibroblasts.Variation in site of lithiation with ring substituent of N ′-aryl-N,N-dimethylureas: application in synthesisPreparation of a chemiluminescent imidoester for the non-radioactive labelling of proteinsLithiation of 3-(Acylamino)-2-unsubstituted-, 3-(Acylamino)-2-ethyl-, and 3-(Acylamino)-2-propyl-4(3H)-quinazolinones: Convenient Syntheses of More Complex Quinazolinones(1)First Synthesis of 3-Mercapto-2(1H)-pyridinone, a Simple Disubstituted Pyridine Useful for Synthesis of the 4-Azaphenoxathiine Ring System and Its Novel Diazaphenoxathiine Analogs: 1,6-Diazaphenoxathiine and 2,6-Diazaphenoxathiine(1)
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Q38586576-C71E84D6-B3E7-4AF2-8531-08FC173D8212Q40280179-5634D316-813A-4CD2-A992-4B95E8534529Q41782679-3BF4E619-CBF8-49E8-A5DD-C409845F306AQ41812700-D4E6D030-78AA-4776-82D9-5D233DF3D7B3Q42145453-CC99FD3B-3814-4AFB-9AE2-5C0808C10350Q42588305-C65783BC-9013-4A3D-ABC0-876D4D3BABE2Q42991514-20D86A07-B7C3-4B51-8121-BDA7D1BDE6A8Q43108935-E4D50DD9-A3EE-4CBF-BD02-192009EBAC04Q43175756-18775682-1ED3-46F9-A27E-3A6964DCDC87Q43175864-C10698EB-DDD7-45EB-9846-7713AEE7A94CQ44067692-471A11ED-6456-4E87-BE1B-34DB52939251Q44554253-D89D2B19-961D-44EC-B295-3EBFB920F891Q44554255-1C643E05-6162-4C76-92BD-89FA7E77D3BFQ44566646-5E51CFF5-960B-42D9-AB08-64A06335BACDQ44790928-23AEF570-6936-4919-9649-9E733069C201Q45125226-8A00F610-72D1-497F-8FE2-E8A982618FAAQ46317719-1F6A33DB-484E-4CAB-9128-323A45A2E6FCQ46486469-D482AB05-1EFE-4609-BC07-B2FD5F1F0073Q46956626-41EAC2A7-29EF-452D-9B72-345C61D328EAQ50623850-4F92536E-FD8E-4578-860C-167D6ED60EA9Q51337870-953D5AC3-4DF8-4957-A9BC-8F679C7AEB64Q53342624-ACC2CE7D-FB11-4F36-8C52-A78E6A85960EQ53352241-28E00587-6BE7-4B8F-96E3-9CA2C38AB7F9Q53580026-477ADBDF-1599-4365-880A-E0295C4EBE65Q53763259-A8E56DFA-E684-4DA3-9D42-3BC6EE21BB93Q53817133-2CE384CC-DAAB-4691-AC8E-ADAFDB522250Q63971941-77708D70-42A3-4EFC-8216-1C4843D182D0Q68186110-55BA4510-C19C-4BBB-88E8-B6D8AA3750D2Q74822433-C549FC7D-79F8-44C2-BE24-C1C395E234B9Q74822438-533BCA88-AF5D-4738-BB0C-2855A3201704
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Keith Smith
@ast
Keith Smith
@en
Keith Smith
@es
Keith Smith
@nl
Keith Smith
@sl
type
label
Keith Smith
@ast
Keith Smith
@en
Keith Smith
@es
Keith Smith
@nl
Keith Smith
@sl
prefLabel
Keith Smith
@ast
Keith Smith
@en
Keith Smith
@es
Keith Smith
@nl
Keith Smith
@sl
P1053
A-2495-2011
P106
P21
P31
P3829
P496
0000-0003-4838-5651