about
Activity of 2-aryl-2-(3-indolyl)acetohydroxamates against drug-resistant cancer cells.Rational design of cyclopropane-based chiral PHOX ligands for intermolecular asymmetric Heck reactionMetal-free transannulation reaction of indoles with nitrostyrenes: a simple practical synthesis of 3-substituted 2-quinolones.One-pot synthesis of GABA amides via the nucleophilic addition of amines to 3,3-disubstituted cyclopropenes.Efficient one-pot synthesis of 1-arylcycloprop-2-ene-1-carboxamides.Thermodynamic control of diastereoselectivity in the formal nucleophilic substitution of bromocyclopropanes.Synthesis of 1,5-Dioxocanes via the Two-Fold C-O Bond Forming Nucleophilic 4+4-Cyclodimerization of Cycloprop-2-en-1-ylmethanols.Palladium-catalyzed highly chemo- and regioselective formal [2+2+2] sequential cycloaddition of alkynes: a renaissance of the well known trimerization reaction?Transition metal-catalyzed hydro-, sila-, and stannastannation of cyclopropenes: stereo- and regioselective approach toward multisubstituted cyclopropyl synthons.Symmetry-enforced conformational control of photochemical reactivity in 2-vinyl-1,3-terphenyl.Highly regiocontrolled Pd-catalyzed cross-coupling reaction of terminal alkynes and allenylphosphine oxides.Highly diastereoselective formal nucleophilic substitution of bromocyclopropanes.Ring-closing photoisomerization of some 2,6-diarylstyrenes.Regiodivergent condensation of 5-alkoxycarbonyl-1H-pyrrol-2,3-diones with cyclic ketazinones en route to spirocyclic scaffolds.Competitive 1,2- and 1,5-hydrogen shifts following 2-vinylbiphenyl photocyclization.One-Pot, Three-Component Assembly of Indoloquinolines: Total Synthesis of Isocryptolepine.Diastereoselectivity control in formal nucleophilic substitution of bromocyclopropanes with oxygen- and sulfur-based nucleophiles.Directed RhI -Catalyzed Asymmetric Hydroboration of Prochiral 1-Arylcycloprop-2-Ene-1-Carboxylic Acid Derivatives.Directed nucleophilic addition of phenoxides to cyclopropenes.B(C6F5)3-catalyzed allylation of secondary benzyl acetates with allylsilanes.Intramolecular nucleophilic addition of carbanions generated from N-benzylamides to cyclopropenes.Desymmetrization of Cyclopropenes via the Potassium-Templated Diastereoselective 7- exo- trig Cycloaddition of Tethered Amino Alcohols toward Enantiopure Cyclopropane-Fused Oxazepanones with Antimycobacterial Activity.Metal-Templated Assembly of Cyclopropane-Fused Diazepanones and Diazecanones via exo-trig Nucleophilic Cyclization of Cyclopropenes with Tethered CarbamatesNitrostyrenes as 1,4-CCNO-dipoles: diastereoselective formal [4+1] cycloaddition of indolesA simple and efficient hydrodehalogenation of 1,1-dihalocyclopropanesA direct reduction of aliphatic aldehyde, acyl chloride, ester, and carboxylic functions into a methyl groupA novel B(C(6)F(5))(3)-catalyzed reduction of alcohols and cleavage of aryl and alkyl ethers with hydrosilanesDirect electrophilic silylation of terminal alkynesHighly efficient B(C(6)F(5))(3)-catalyzed hydrosilylation of olefinsCatalytic enantioselective hydrostannation of cyclopropenesRemarkable stereoelectronic control in the Lewis base assisted [2,3]-rearrangement of cyclopropenylmethyl phosphinitesCan polarization of triple bond in tolanes be deduced from 13C NMR shifts? Re-evaluation of factors affecting regiochemistry of the palladium-catalyzed hydrostannation of alkynesTransition metal chemistry of cyclopropenes and cyclopropanesHighly diastereo- and regioselective transition metal-catalyzed additions of metal hydrides and bimetallic species to cyclopropenes: easy access to multisubstituted cyclopropanesDirect palladium-catalyzed arylation of cyclopropenesPalladium-catalyzed hydrophosphorylation and hydrophosphinylation of cyclopropenesRhodium-catalyzed hydroformylation of cyclopropenesSolvent dependent photocyclization and photophysics of some 2-ethynylbiphenylsFormal nucleophilic substitution of bromocyclopropanes with azolesFormal nucleophilic substitution of bromocyclopropanes with amides en route to conformationally constrained β-amino acid derivatives
P50
Q27335770-B8CEAE0A-FBE4-476E-9F7B-FD34928C3317Q34083149-A40C52C3-AA22-4B17-8C1B-3555F75A74ABQ37096674-94B83C1B-FC2E-4476-A7A4-14620453031EQ38354402-2AFCCFA1-FA85-4E44-99E9-DE74381BD42DQ42769394-A7A41E19-837C-4514-BE88-67CC6F8AA3CCQ43135560-E1A5C75D-FAF6-403E-BD1F-EEB0925EEFF7Q43164755-5B315A02-4018-416D-8371-3DD55BDEBE77Q43576354-AB3FE42B-D7C4-4975-BED1-743BCE99BA94Q44150503-D92E2C62-6D6D-446C-A255-45134D089182Q44215911-1249BC9A-3F83-431D-ABFE-C6B1081941C4Q44534959-79BBB28D-6B3D-42E2-AE29-D901DA03241CQ46026732-8970ADA5-87F5-4FF7-886D-07B7E23EEF07Q46602950-06B3751B-0897-4BA7-B5DB-0B37B83A5BE6Q46645454-299D97E3-520E-4351-BFEC-E409A5AF4A24Q46832379-BEB5080A-0932-4EC1-941D-6A3AE0FA54A9Q48171205-6772E40E-AAA3-43E3-B204-4E74E98432BCQ48274053-69AF1078-9321-4F12-B1D6-86F90FDB67F8Q48309011-DF7ED684-F1F7-42F7-976B-9A725CB10352Q48334339-5220486C-1D02-4502-8A6C-E1A5CC09DA58Q49771436-21FFDEEF-DC1B-4FC3-B7D1-5F55AA57B1FDQ49834131-85B34A61-D42D-47C7-B227-BE55FCDC67A5Q52562058-8F5C76C2-7CC3-47D8-A59E-82C173B57E1CQ57792693-6BD5CA27-13DC-4908-8D72-4956A300D273Q58562440-02BDF7C3-81A1-4C6A-8536-750DDD718343Q63362683-D87F7E11-E1EE-4A2A-9548-4BB705983B3CQ73655007-46462871-437D-4C03-AFF4-80091A28410AQ74316189-9C986D6B-BF84-41FC-AD92-FD12B3338647Q75351607-762D94F4-661F-4D4E-A44B-583E432CECA6Q77767453-60473B84-D94E-4DDD-907C-0A2EB0B8E018Q79814213-DE4F689F-96DB-47FA-B1C7-86D3BD2A5286Q79895381-ED9CA419-AEE1-4DD1-A6D1-DF9809A7A9FCQ80392071-12CD1FD0-76F6-4A24-8DDF-884ACA059EA5Q80592410-C722A54A-5906-4706-B1F3-FA811EAB8655Q81438326-F98BCA33-BDDF-4AF7-9E3A-7CC1DAE75F99Q81531135-B6E77547-A867-4610-BBAE-E01BEB617F2EQ81546913-11D5F520-CFD1-4288-9129-CD1F3E72008AQ82002971-44D39AAF-66D8-4FFB-A605-49EB915F7826Q83047256-E7736654-AFC1-4A57-A811-181CC5130F5DQ83643354-A898A39D-CE7B-46DD-AC95-D37A463A62F2Q84777973-E86832E1-7270-4B19-AABC-758DE9EE96D1
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Michael Rubin
@ast
Michael Rubin
@en
Michael Rubin
@es
Michael Rubin
@nl
Michael Rubin
@sl
type
label
Michael Rubin
@ast
Michael Rubin
@en
Michael Rubin
@es
Michael Rubin
@nl
Michael Rubin
@sl
altLabel
Michael A. Rubin
@en
prefLabel
Michael Rubin
@ast
Michael Rubin
@en
Michael Rubin
@es
Michael Rubin
@nl
Michael Rubin
@sl
P1053
N-5699-2016
P106
P1153
36546833600
P21
P31
P3829
P496
0000-0002-1668-9311