| Year |
Citation |
Score |
| 2022 |
Straub H, Ryabchuk P, Rubina M, Rubin M. Preparation of Chiral Enantioenriched Densely Substituted Cyclopropyl Azoles, Amines, and Ethers via Formal S2' Substitution of Bromocylopropanes. Molecules (Basel, Switzerland). 27. PMID 36296663 DOI: 10.3390/molecules27207069 |
0.672 |
|
| 2022 |
Aksenov AV, Kirilov NK, Arutiunov NA, Aksenov DA, Kuzminov IK, Aksenov NA, Turner DN, Rogelj S, Kornienko A, Rubin M. Reductive Cleavage of 4'-Spiro[indole-3,5'-isoxazoles] En Route to 2-(1-Indol-3-yl)acetamides with Anticancer Activities. The Journal of Organic Chemistry. PMID 36260110 DOI: 10.1021/acs.joc.2c01627 |
0.389 |
|
| 2022 |
Aksenov AV, Arutiunov NA, Aksenov DA, Samovolov AV, Kurenkov IA, Aksenov NA, Aleksandrova EA, Momotova DS, Rubin M. A Convenient Way to Quinoxaline Derivatives through the Reaction of 2-(3-Oxoindolin-2-yl)-2-phenylacetonitriles with Benzene-1,2-diamines. International Journal of Molecular Sciences. 23. PMID 36232422 DOI: 10.3390/ijms231911120 |
0.343 |
|
| 2022 |
Aksenov NA, Aksenov AV, Prityko LA, Aksenov DA, Aksenova DS, Nobi MA, Rubin M. Oxidative Cyclization of 4-(2-Aminophenyl)-4-oxo-2-phenylbutanenitriles into 2-(3-Oxoindolin-2-ylidene)acetonitriles. Acs Omega. 7: 14345-14356. PMID 35573208 DOI: 10.1021/acsomega.2c01238 |
0.327 |
|
| 2022 |
Aksenov NA, Aksenov AV, Kurenkov IA, Kirillov NK, Aksenov DA, Arutiunov NA, Aksenova DS, Rubin M. One-Pot Synthesis of ()-2-(3-Oxoindolin-2-ylidene)-2-arylacetonitriles. Molecules (Basel, Switzerland). 27. PMID 35566159 DOI: 10.3390/molecules27092808 |
0.371 |
|
| 2022 |
Aksenov AV, Aleksandrova EV, Aksenov DA, Aksenova AA, Aksenov NA, Nobi MA, Rubin M. Synthetic Studies toward 1,2,3,3a,4,8b-Hexahydropyrrolo[3,2-]indole Core. Unusual Fragmentation with 1,2-Aryl Shift. The Journal of Organic Chemistry. 87: 1434-1444. PMID 34990543 DOI: 10.1021/acs.joc.1c02753 |
0.311 |
|
| 2021 |
Aksenov AV, Aksenov DA, Aksenov NA, Skomorokhov AA, Aleksandrova EV, Rubin M. Preparation of spiro[indole-3,5'-isoxazoles] Grignard conjugate addition/spirocyclization sequence. Rsc Advances. 11: 1783-1793. PMID 35424118 DOI: 10.1039/d0ra10219a |
0.344 |
|
| 2021 |
Aksenov AV, Kirilov NK, Aksenov NA, Aksenov DA, Sorokina EA, Lower C, Rubin M. Electrophilically Activated Nitroalkanes in Double Annulation of [1,2,4]Triazolo[4,3-]quinolines and 1,3,4-Oxadiazole Rings. Molecules (Basel, Switzerland). 26. PMID 34577163 DOI: 10.3390/molecules26185692 |
0.373 |
|
| 2021 |
Aksenov AV, Grishin IY, Aksenov NA, Malyuga VV, Aksenov DA, Nobi MA, Rubin M. Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines. Molecules (Basel, Switzerland). 26. PMID 34299549 DOI: 10.3390/molecules26144274 |
0.376 |
|
| 2020 |
Aksenov NA, Aksenov DA, Arutiunov NA, Aksenova DS, Aksenov AV, Rubin M. Unexpected cyclization of -nitrochalcones into 2-alkylideneindolin-3-ones. Rsc Advances. 10: 18440-18450. PMID 35517232 DOI: 10.1039/d0ra03520c |
0.374 |
|
| 2020 |
Shcherbakov SS, Magometov AY, Shcherbakova VY, Aksenov AV, Domenyuk DA, Zelensky VA, Rubin M. Electrophilic alkylation of arenes with 5-bromopyrimidine en route to 4-aryl-5-alkynylpyrimidines. Rsc Advances. 10: 10315-10321. PMID 35498620 DOI: 10.1039/d0ra01335h |
0.402 |
|
| 2020 |
Aksenov NA, Aksenov DA, Skomorokhov AA, Prityko LA, Aksenov AV, Griaznov GD, Rubin M. Synthesis of 2-(1H-Indol-2-yl)acetamides via Bronsted Acid-Assisted Cyclization Cascade. The Journal of Organic Chemistry. PMID 32881523 DOI: 10.1021/Acs.Joc.0C01344 |
0.389 |
|
| 2020 |
Aksenov NA, Aksenov AV, Kirilov NK, Arutiunov NA, Aksenov DA, Maslivetc V, Zhao Z, Du L, Rubin M, Kornienko A. Nitroalkanes as electrophiles: synthesis of triazole-fused heterocycles with neuroblastoma differentiation activity. Organic & Biomolecular Chemistry. PMID 32813002 DOI: 10.1039/D0Ob01007C |
0.423 |
|
| 2020 |
Zhulanov VE, Vigovskaya VA, Dmitriev MV, Silaichev PS, Maslivets AN, Rubin M. Dipyrazolodioxadiazocines as shelf-stable "ready-to-use" precursors for an in situ generation of enolate-iminium 1,4-dipoles: a straightforward atom-economical approach to pyrazolo[5,1-d][1,3,5]dioxazines. Organic & Biomolecular Chemistry. PMID 32323682 DOI: 10.1039/D0Ob00451K |
0.395 |
|
| 2020 |
Yamanushkin P, Smith SP, Petillo PA, Rubin M. Cyclopropene-Templated Assembly of Medium Cycles via Ru-Catalyzed Ring-Closing Metathesis. Organic Letters. 22: 3542-3546. PMID 32323545 DOI: 10.1021/Acs.Orglett.0C00974 |
0.463 |
|
| 2020 |
Aksenov NA, Aksenov AV, Ovcharov SN, Aksenov DA, Rubin M. Electrophilically Activated Nitroalkanes in Reactions With Carbon Based Nucleophiles. Frontiers in Chemistry. 8: 77. PMID 32117896 DOI: 10.3389/Fchem.2020.00077 |
0.342 |
|
| 2020 |
Aksenov NA, Aksenov DA, Arutiunov NA, Aksenova DS, Aksenov AV, Rubin M. Unexpected cyclization of ortho-nitrochalcones into 2-alkylideneindolin-3-ones Rsc Advances. 10: 18440-18450. DOI: 10.1039/D0Ra03520C |
0.483 |
|
| 2020 |
Shcherbakov SS, Magometov AY, Shcherbakova VY, Aksenov AV, Domenyuk DA, Zelensky VA, Rubin M. Electrophilic alkylation of arenes with 5-bromopyrimidine en route to 4-aryl-5-alkynylpyrimidines Rsc Advances. 10: 10315-10321. DOI: 10.1039/D0Ra01335H |
0.5 |
|
| 2019 |
Aksenov AV, Aksenov NA, Arutiunov NA, Malyuga VV, Ovcharov SN, Rubin M. Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines. Rsc Advances. 9: 39458-39465. PMID 35540681 DOI: 10.1039/c9ra08630g |
0.389 |
|
| 2019 |
Aksenov AV, Khamraev V, Aksenov NA, Kirilov NK, Domenyuk DA, Zelensky VA, Rubin M. Electrophilic activation of nitroalkanes in efficient synthesis of 1,3,4-oxadiazoles. Rsc Advances. 9: 6636-6642. PMID 35518500 DOI: 10.1039/c9ra00976k |
0.365 |
|
| 2019 |
Kobelev AI, Tretyakov NA, Stepanova EE, Dmitriev MV, Rubin M, Maslivets AN. Facile regiodivergent synthesis of spiro pyrrole-substituted pseudothiohydantoins and thiohydantoins via reaction of []-fused 1-pyrrole-2,3-diones with thiourea. Beilstein Journal of Organic Chemistry. 15: 2864-2871. PMID 31839832 DOI: 10.3762/Bjoc.15.280 |
0.505 |
|
| 2019 |
Galeev AR, Dmitriev MV, Mokrushin IG, Mashevskaya IV, Maslivets AN, Rubin M. Synthesis of meta-substituted anilines via a three-component reaction of acetone, amines, and 1,3-diketones. Organic & Biomolecular Chemistry. PMID 31746918 DOI: 10.1039/C9Ob02120E |
0.464 |
|
| 2019 |
Aksenov AV, Aksenov DA, Aksenov NA, Aleksandrova EV, Rubin M. Preparation of Stereo-Defined 2-(3-Oxoindolin-2-yl)-2-Arylacetonitriles via One-Pot Reaction of Indoles with Nitroalkenes. The Journal of Organic Chemistry. PMID 31502836 DOI: 10.1021/Acs.Joc.9B01874 |
0.497 |
|
| 2019 |
Aksenov AV, Aksenov DA, Arutiunov NA, Aksenov NA, Aleksandrova EV, Zhao Z, Du L, Kornienko A, Rubin M. Synthesis of Spiro[indole-3,5'-isoxazoles] with Anticancer Activity via a Formal (4+1)-Spirocyclization of Nitroalkenes to Indoles. The Journal of Organic Chemistry. PMID 31070030 DOI: 10.1021/Acs.Joc.9B00808 |
0.344 |
|
| 2019 |
Aksenov AV, Aksenov NA, Arutiunov NA, Malyuga VV, Ovcharov SN, Rubin M. Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines Rsc Advances. 9: 39458-39465. DOI: 10.1039/C9Ra08630G |
0.489 |
|
| 2019 |
Aksenov AV, Khamraev V, Aksenov NA, Kirilov NK, Domenyuk DA, Zelensky VA, Rubin M. Electrophilic activation of nitroalkanes in efficient synthesis of 1,3,4-oxadiazoles Rsc Advances. 9: 6636-6642. DOI: 10.1039/C9Ra00976K |
0.469 |
|
| 2018 |
Aksenov NA, Aksenov AV, Kornienko A, De Carvalho A, Mathieu V, Aksenov DA, Ovcharov SN, Griaznov GD, Rubin M. A nitroalkane-based approach to one-pot three-component synthesis of isocryptolepine and its analogs with potent anti-cancer activities. Rsc Advances. 8: 36980-36986. PMID 35558925 DOI: 10.1039/c8ra08155g |
0.303 |
|
| 2018 |
Aksenov AV, Aksenov NA, Aksenov DA, Khamraev VF, Rubin M. Nitrostyrenes as 1,4-CCNO-dipoles: diastereoselective formal [4+1] cycloaddition of indoles. Chemical Communications (Cambridge, England). PMID 30411750 DOI: 10.1039/C8Cc07451H |
0.428 |
|
| 2018 |
Maslivetc VA, Frolova LV, Rogelj S, Maslivetc AA, Rubina M, Rubin M. Metal-Templated Assembly of Cyclopropane-Fused Diazepanones and Diazecanones via exo-trig Nucleophilic Cyclization of Cyclopropenes with Tethered Carbamates. The Journal of Organic Chemistry. PMID 30354138 DOI: 10.1021/Acs.Joc.8B02062 |
0.719 |
|
| 2018 |
Yamanushkin P, Lu-Diaz M, Edwards A, Aksenov NA, Rubina M, Rubin M. Correction: Directed nucleophilic addition of phenoxides to cyclopropenes. Organic & Biomolecular Chemistry. PMID 30059124 DOI: 10.1039/C8Ob90109K |
0.6 |
|
| 2018 |
Edwards A, Rubin M. Directed Cu(I)-Catalyzed Carbomagnesiation of 1-Arylcycloprop-2-ene-1-carboxamides en route to Densely Substituted Functionalized Cyclopropanes. The Journal of Organic Chemistry. PMID 29929370 DOI: 10.1021/Acs.Joc.8B01063 |
0.445 |
|
| 2018 |
Aksenov AV, Aksenov DA, Griaznov GD, Aksenov NA, Voskressensky LG, Rubin M. Unexpected cyclization of 2-(2-aminophenyl)indoles with nitroalkenes to furnish indolo[3,2-c]quinolines. Organic & Biomolecular Chemistry. PMID 29808901 DOI: 10.1039/C8Ob00588E |
0.438 |
|
| 2018 |
Maslivetc VA, Turner DN, McNair KN, Frolova LV, Rogelj S, Maslivetc AA, Aksenov NA, Rubina M, Rubin M. Desymmetrization of Cyclopropenes via the Potassium-Templated Diastereoselective 7-exo-trig Cycloaddition of Tethered Amino Alcohols toward Enantiopure Cyclopropane-Fused Oxazepanones with Anti-Mycobacterial Activity. The Journal of Organic Chemistry. PMID 29696970 DOI: 10.1021/Acs.Joc.8B00640 |
0.686 |
|
| 2018 |
Aksenov NA, Aksenov A, Kornienko A, De Carvalho A, Mathieu V, Aksenov DA, Ovcharov SN, Griaznov GD, Rubin M. A nitroalkane-based approach to one-pot three-component synthesis of isocryptolepine and its analogs with potent anti-cancer activities Rsc Advances. 8: 36980-36986. DOI: 10.1039/C8Ra08155G |
0.343 |
|
| 2018 |
Aksenov AV, Shcherbakov SV, Lobach IV, Voskressensky LG, Rubin M. Synthesis of 7‐Bromo‐1,3‐diazapyrenes European Journal of Organic Chemistry. 2018: 4121-4127. DOI: 10.1002/Ejoc.201800703 |
0.389 |
|
| 2017 |
Maslivetc V, Barrett C, Aksenov NA, Rubina M, Rubin M. Intramolecular nucleophilic addition of carbanions generated from N-benzylamides to cyclopropenes. Organic & Biomolecular Chemistry. PMID 29242861 DOI: 10.1039/C7Ob02068F |
0.708 |
|
| 2017 |
Edwards A, Rubin M, Rubina M. Directed Rh(I)-Catalyzed Asymmetric Hydroboration of Prochiral 1-Arylcycloprop-2-ene-1-carboxylic Acid Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29134770 DOI: 10.1002/Chem.201704443 |
0.722 |
|
| 2017 |
Dubovtsev AY, Dmitriev MV, Maslivets АN, Rubin M. Regiodivergent condensation of 5-alkoxycarbonyl-1H-pyrrol-2,3-diones with cyclic ketazinones en route to spirocyclic scaffolds. Beilstein Journal of Organic Chemistry. 13: 2179-2185. PMID 29114325 DOI: 10.3762/Bjoc.13.218 |
0.437 |
|
| 2017 |
Yamanushkin P, Lu-Diaz M, Edwards A, Aksenov NA, Rubina M, Rubin M. Directed nucleophilic addition of phenoxides to cyclopropenes. Organic & Biomolecular Chemistry. PMID 28920624 DOI: 10.1039/C7Ob01785E |
0.666 |
|
| 2017 |
Aksenov AV, Aksenov DA, Orazova NA, Aksenov NA, Griaznov GD, De Carvalho A, Kiss R, Mathieu V, Kornienko A, Rubin M. One-Pot, Three-Component Assembly of Indoloquinolines: Total Synthesis of Isocryptolepine. The Journal of Organic Chemistry. PMID 28253622 DOI: 10.1021/Acs.Joc.6B03084 |
0.399 |
|
| 2017 |
Aksenov AV, Ovcharov DS, Aksenov NA, Aksenov DA, Nadein ON, Rubin M. Dual role of polyphosphoric acid-activated nitroalkanes in oxidative peri-annulations: efficient synthesis of 1,3,6,8-tetraazapyrenes Rsc Advances. 7: 29927-29932. DOI: 10.1039/C7Ra04751G |
0.426 |
|
| 2017 |
Aksenov AV, Shcherbakov SV, Lobach IV, Aksenova IV, Rubin M. Pyrimidines as Surrogates for 1,3‐Dicarbonyl Compounds in peri Annulation of Perimidines en Route to 1,3‐Diazapyrenes European Journal of Organic Chemistry. 2017: 1666-1673. DOI: 10.1002/Ejoc.201601589 |
0.426 |
|
| 2016 |
Ryabchuk P, Matheny JP, Rubina M, Rubin M. Templated Assembly of Chiral Medium-Sized Cyclic Ethers via 8-endo-trig Nucleophilic Cyclization of Cyclopropenes. Organic Letters. 18: 6272-6275. PMID 27978680 DOI: 10.1021/Acs.Orglett.6B03068 |
0.719 |
|
| 2016 |
Alnasleh BK, Rubina M, Rubin M. Templated assembly of medium cyclic ethers via exo-trig nucleophilic cyclization of cyclopropenes. Chemical Communications (Cambridge, England). PMID 27210442 DOI: 10.1039/C6Cc02178F |
0.713 |
|
| 2016 |
Edwards A, Rubin M. Efficient one-pot synthesis of 1-arylcycloprop-2-ene-1-carboxamides. Organic & Biomolecular Chemistry. PMID 26864495 DOI: 10.1039/C6Ob00156D |
0.447 |
|
| 2016 |
Edwards A, Rubina M, Rubin M. Nucleophilic Addition of Cyclopropenes Current Organic Chemistry. 20: 1862-1877. DOI: 10.2174/1385272820666160331235409 |
0.715 |
|
| 2016 |
Zhulanov VE, Dmitriev MV, Maslivets AN, Rubin M. New method for in situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions Rsc Advances. 6: 90239-90247. DOI: 10.1039/C6Ra21981K |
0.437 |
|
| 2016 |
Aksenov AV, Aksenov NA, Dzhandigova ZV, Aksenov DA, Voskressensky LG, Nenajdenko VG, Rubin M. Direct reductive coupling of indoles to nitrostyrenes en route to (indol-3-yl)acetamides Rsc Advances. 6: 93881-93886. DOI: 10.1039/C6Ra21399E |
0.366 |
|
| 2016 |
Aksenov AV, Aksenov NA, Ovcharov DS, Aksenov DA, Griaznov G, Voskressensky LG, Rubin M. Rational design of an efficient one-pot synthesis of 6H-pyrrolo[2,3,4-gh]perimidines in polyphosphoric acid Rsc Advances. 6: 82425-82431. DOI: 10.1039/C6Ra17269E |
0.437 |
|
| 2016 |
Dubovtsev AY, Silaichev PS, Nazarov MA, Dmitriev MV, Maslivets AN, Rubin M. Spiro-condensation of 5-methoxycarbonyl-1H-pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolines Rsc Advances. 6: 84730-84737. DOI: 10.1039/C6Ra16889B |
0.458 |
|
| 2016 |
Aksenov AV, Magamadova MH, Lobach DA, Aksenova IV, Malikova IV, Rubin M. Erratum to: peri Annelation of Perimidines in Reactions with 1,3-Dicarbonyl Compounds Chemistry of Heterocyclic Compounds. 52: 350-350. DOI: 10.1007/S10593-016-1889-4 |
0.345 |
|
| 2016 |
Edwards A, Rubina M, Rubin M. ChemInform Abstract: Nucleophilic Addition of Cyclopropenes Cheminform. 47. DOI: 10.1002/chin.201643221 |
0.644 |
|
| 2016 |
Edwards A, Rubin M. ChemInform Abstract: Efficient One-Pot Synthesis of 1-Arylcycloprop-2-ene-1-carboxamides. Cheminform. 47. DOI: 10.1002/CHIN.201628076 |
0.31 |
|
| 2015 |
Edwards A, Bennin T, Rubina M, Rubin M. Synthesis of 1,5-Dioxocanes via the Two-Fold C-O Bond Forming Nucleophilic 4+4-Cyclodimerization of Cycloprop-2-en-1-ylmethanols. Rsc Advances. 5: 71849-71853. PMID 26594355 DOI: 10.1039/C5Ra14077C |
0.659 |
|
| 2015 |
Maslivetc VA, Rubina M, Rubin M. One-pot synthesis of GABA amides via the nucleophilic addition of amines to 3,3-disubstituted cyclopropenes. Organic & Biomolecular Chemistry. 13: 8993-5. PMID 26243009 DOI: 10.1039/C5Ob01462J |
0.686 |
|
| 2015 |
Aksenov AV, Smirnov AN, Aksenov NA, Bijieva AS, Aksenova IV, Rubin M. Benzimidazoles and benzoxazoles via the nucleophilic addition of anilines to nitroalkanes. Organic & Biomolecular Chemistry. 13: 4289-95. PMID 25758157 DOI: 10.1039/C5Ob00131E |
0.427 |
|
| 2015 |
Aksenov AV, Aksenov NA, Dzhandigova ZV, Aksenov DA, Rubin M. Nitroalkenes as surrogates for cyanomethylium species in a one-pot synthesis of non-symmetric diarylacetonitriles Rsc Advances. 5: 106492-106497. DOI: 10.1039/C5Ra20953F |
0.432 |
|
| 2015 |
Aksenov AV, Aksenov NA, Orazova NA, Aksenov DA, Dmitriev MV, Rubin M. Direct metal-free synthesis of diarylamines from 2-nitropropane via the twofold C-H functionalization of arenes Rsc Advances. 5: 84849-84855. DOI: 10.1039/C5Ra17668A |
0.394 |
|
| 2015 |
Aksenov NA, Aksenov AV, Nadein ON, Aksenov DA, Smirnov AN, Rubin M. One-pot synthesis of benzoxazoles via the metal-free ortho-C-H functionalization of phenols with nitroalkanes Rsc Advances. 5: 71620-71626. DOI: 10.1039/C5Ra15128G |
0.371 |
|
| 2015 |
Edwards A, Bennin T, Rubina M, Rubin M. Synthesis of 1,5-dioxocanes via the two-fold C-O bond forming nucleophilic 4 + 4-cyclodimerization of cycloprop-2-en-1-ylmethanols Rsc Advances. 5: 71849-71853. DOI: 10.1039/c5ra14077c |
0.617 |
|
| 2015 |
Maslivetc VA, Rubina M, Rubin M. One-pot synthesis of GABA amides via the nucleophilic addition of amines to 3,3-disubstituted cyclopropenes Organic and Biomolecular Chemistry. 13: 8993-8995. DOI: 10.1039/c5ob01462j |
0.624 |
|
| 2015 |
Aksenov AV, Smirnov AN, Aksenov NA, Aksenova IV, Matheny JP, Rubin M. Metal-free ring expansion of indoles with nitroalkenes: A simple, modular approach to 3-substituted 2-quinolones Rsc Advances. 5: 8647-8656. DOI: 10.1039/C4Ra14406F |
0.466 |
|
| 2015 |
Edwards A, Rubin M. Synthesis of 1-arylcycloprop-2-ene carboxylates with non-substituted double bond via a Rh(II)-catalyzed cyclopropenation of trimethylsilylacetylene with coarsely purified aryldiazoacetates Tetrahedron. DOI: 10.1016/J.Tet.2015.03.120 |
0.439 |
|
| 2015 |
Silaichev PS, Filimonov VO, Slepukhin PA, Rubin M, Maslivets AN. Diastereoselective synthesis of indolindiones by formal [5+1] double michael cycloaddition to 4-cinnamoylpyrrolediones European Journal of Organic Chemistry. 2015: 2739-2744. DOI: 10.1002/Ejoc.201500141 |
0.492 |
|
| 2014 |
Aksenov AV, Smirnov AN, Aksenov NA, Aksenova IV, Bijieva AS, Rubin M. Highly efficient modular metal-free synthesis of 3-substituted 2-quinolones. Organic & Biomolecular Chemistry. 12: 9786-8. PMID 25371015 DOI: 10.1039/C4Ob02131B |
0.489 |
|
| 2014 |
Rubina M, Sherrill WM, Barkov AY, Rubin M. Rational design of cyclopropane-based chiral PHOX ligands for intermolecular asymmetric Heck reaction. Beilstein Journal of Organic Chemistry. 10: 1536-48. PMID 25161709 DOI: 10.3762/Bjoc.10.158 |
0.676 |
|
| 2014 |
Edwards A, Ryabchuk P, Barkov A, Rubina M, Rubin M. Preparative resolution of bromocyclopropylcarboxylic acids Tetrahedron Asymmetry. 25: 1537-1549. DOI: 10.1016/J.Tetasy.2014.10.017 |
0.651 |
|
| 2014 |
Aksenov AV, Magamadova MH, Lobach DA, Aksenova IV, Malikova IV, Rubin M. Peri annelation of perimidines in reactions with 1,3-dicarbonyl compounds Chemistry of Heterocyclic Compounds. 50: 1298-1304. DOI: 10.1007/S10593-014-1592-2 |
0.348 |
|
| 2014 |
Shcherbakov SV, Lobach DA, Rubin M, Aksenov AV. Synthesis of N-phenyl-1,5,7-triazacyclopenta[cd]- phenalenes by the reaction of 1H-perimidine carbonyl derivatives with nitrobenzene Chemistry of Heterocyclic Compounds. 50: 757-760. DOI: 10.1007/S10593-014-1531-2 |
0.365 |
|
| 2013 |
Ryabchuk P, Edwards A, Gerasimchuk N, Rubina M, Rubin M. Dual control of the selectivity in the formal nucleophilic substitution of bromocyclopropanes en route to densely functionalized, chirally rich cyclopropyl derivatives. Organic Letters. 15: 6010-3. PMID 24261655 DOI: 10.1021/Ol4027792 |
0.708 |
|
| 2013 |
Aksenov AV, Smirnov AN, Aksenov NA, Aksenova IV, Frolova LV, Kornienko A, Magedov IV, Rubin M. Metal-free transannulation reaction of indoles with nitrostyrenes: a simple practical synthesis of 3-substituted 2-quinolones. Chemical Communications (Cambridge, England). 49: 9305-7. PMID 23999797 DOI: 10.1039/C3Cc45696J |
0.475 |
|
| 2013 |
Banning JE, Gentillon J, Ryabchuk PG, Prosser AR, Rogers A, Edwards A, Holtzen A, Babkov IA, Rubina M, Rubin M. Formal substitution of bromocyclopropanes with nitrogen nucleophiles. The Journal of Organic Chemistry. 78: 7601-16. PMID 23845068 DOI: 10.1021/Jo4011798 |
0.707 |
|
| 2012 |
Ryabchuk P, Rubina M, Xu J, Rubin M. Formal nucleophilic substitution of bromocyclopropanes with azoles. Organic Letters. 14: 1752-5. PMID 22416670 DOI: 10.1021/Ol300352Z |
0.706 |
|
| 2012 |
Rubina M, Rubin M. Rearrangement of cyclopropylborane into boretane Chemistry of Heterocyclic Compounds. 1-15. DOI: 10.1007/S10593-012-1060-9 |
0.643 |
|
| 2012 |
Rubin M, Ryabchuk PG. Rearrangements of cyclopropenes into five-membered aromatic heterocycles: Mechanistic aspect Chemistry of Heterocyclic Compounds. 48: 126-138. DOI: 10.1007/S10593-012-0976-4 |
0.45 |
|
| 2011 |
Banning JE, Prosser AR, Alnasleh BK, Smarker J, Rubina M, Rubin M. Diastereoselectivity control in formal nucleophilic substitution of bromocyclopropanes with oxygen- and sulfur-based nucleophiles. The Journal of Organic Chemistry. 76: 3968-86. PMID 21462995 DOI: 10.1021/Jo200368A |
0.708 |
|
| 2010 |
Prosser AR, Banning JE, Rubina M, Rubin M. Formal nucleophilic substitution of bromocyclopropanes with amides en route to conformationally constrained β-amino acid derivatives. Organic Letters. 12: 3968-71. PMID 20726591 DOI: 10.1021/Ol101228K |
0.693 |
|
| 2010 |
Banning JE, Prosser AR, Rubin M. Thermodynamic control of diastereoselectivity in the formal nucleophilic substitution of bromocyclopropanes. Organic Letters. 12: 1488-91. PMID 20218634 DOI: 10.1021/Ol100187C |
0.391 |
|
| 2010 |
Kim R, Sherrill WM, Rubin M. Ring-retentive deprotonation of cyclopropene-3-carboxamides Tetrahedron. 66: 4947-4953. DOI: 10.1016/J.Tet.2010.04.123 |
0.348 |
|
| 2010 |
Rubin M, Schwier T, Gevorgyan V. ChemInform Abstract: Highly Efficient B(C6F5)3-Catalyzed Hydrosilylation of Olefins. Cheminform. 33: no-no. DOI: 10.1002/chin.200233194 |
0.789 |
|
| 2010 |
KUDREVICH SV, RUBIN MA, TARABAEVA OG, SURMINA LS, BERD MS, BOLESOV IG. ChemInform Abstract: Simple Synthesis of 3-Methylcyclopropene-3-carboxylates. Cheminform. 26: no-no. DOI: 10.1002/chin.199534113 |
0.318 |
|
| 2009 |
Alnasleh BK, Sherrill WM, Rubina M, Banning J, Rubin M. Highly diastereoselective formal nucleophilic substitution of bromocyclopropanes. Journal of the American Chemical Society. 131: 6906-7. PMID 19413323 DOI: 10.1021/Ja900634M |
0.735 |
|
| 2009 |
Alnasleh BK, Sherrill WM, Rubina M, Banning J, Rubin M. Formal Nucleophilic Substitution of Bromocyclopropanes Synfacts. 2009: 876-876. DOI: 10.1055/S-0029-1217442 |
0.442 |
|
| 2009 |
Sherrill WM, Kim R, Rubin M. Synthesis of cyclopropenes via 1,2-elimination of bromocyclopropanes catalyzed by crown ether Synthesis. 1477-1484. DOI: 10.1055/S-0028-1088122 |
0.459 |
|
| 2008 |
Sherrill WM, Rubin M. Rhodium-catalyzed hydroformylation of cyclopropenes. Journal of the American Chemical Society. 130: 13804-9. PMID 18803386 DOI: 10.1021/Ja805059F |
0.416 |
|
| 2008 |
Alnasleh BK, Sherrill WM, Rubin M. Palladium-catalyzed hydrophosphorylation and hydrophosphinylation of cyclopropenes. Organic Letters. 10: 3231-4. PMID 18588304 DOI: 10.1021/Ol8011138 |
0.461 |
|
| 2008 |
Rubina M, Sherrill WM, Rubin M. Dramatic stereo- and enantiodivergency in the intermolecular asymmetric heck reaction catalyzed by palladium complexes with cyclopropane-based PHOX ligands Organometallics. 27: 6393-6395. DOI: 10.1021/Om801051D |
0.674 |
|
| 2008 |
Sherrill WM, Kim R, Rubin M. Improved preparative route toward 3-arylcyclopropenes Tetrahedron. 64: 8610-8617. DOI: 10.1016/J.Tet.2008.06.087 |
0.458 |
|
| 2007 |
Rubina M, Woodward EW, Rubin M. Remarkable stereoelectronic control in the Lewis base assisted [2,3]-rearrangement of cyclopropenylmethyl phosphinites. Organic Letters. 9: 5501-4. PMID 18020352 DOI: 10.1021/Ol702473S |
0.688 |
|
| 2007 |
Trofimov A, Rubina M, Rubin M, Gevorgyan V. Highly diastereo- and regioselective transition metal-catalyzed additions of metal hydrides and bimetallic species to cyclopropenes: easy access to multisubstituted cyclopropanes. The Journal of Organic Chemistry. 72: 8910-20. PMID 17935353 DOI: 10.1021/Jo701855C |
0.789 |
|
| 2007 |
Rubin M, Rubina M, Gevorgyan V. Transition metal chemistry of cyclopropenes and cyclopropanes. Chemical Reviews. 107: 3117-79. PMID 17622181 DOI: 10.1021/Cr050988L |
0.73 |
|
| 2006 |
Lewis FD, Karagiannis PC, Sajimon MC, Lovejoy KS, Zuo X, Rubin M, Gevorgyan V. Solvent dependent photocyclization and photophysics of some 2-ethynylbiphenyls. Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society For Photobiology. 5: 369-75. PMID 16583016 DOI: 10.1039/B601751G |
0.668 |
|
| 2006 |
Lewis FD, Crompton EM, Sajimon MC, Gevorgyan V, Rubin M. Ring-closing photoisomerization of some 2,6-diarylstyrenes. Photochemistry and Photobiology. 82: 119-22. PMID 16022562 DOI: 10.1562/2005-05-26-Ra-545 |
0.674 |
|
| 2006 |
Rubin M, Rubina M, Gevorgyan V. Recent advances in cyclopropene chemistry Synthesis. 1221-1245. DOI: 10.1055/S-2006-926404 |
0.739 |
|
| 2005 |
Lewis FD, Sajimon MC, Zuo X, Rubin M, Gevorgyan V. Competitive 1,2- and 1,5-hydrogen shifts following 2-vinylbiphenyl photocyclization. The Journal of Organic Chemistry. 70: 10447-52. PMID 16323856 DOI: 10.1021/Jo051730Y |
0.638 |
|
| 2005 |
Rubin M, Trofimov A, Gevorgyan V. Can polarization of triple bond in tolanes be deduced from 13C NMR shifts? Re-evaluation of factors affecting regiochemistry of the palladium-catalyzed hydrostannation of alkynes. Journal of the American Chemical Society. 127: 10243-9. PMID 16028935 DOI: 10.1021/Ja051274V |
0.724 |
|
| 2005 |
Chuprakov S, Rubin M, Gevorgyan V. Direct palladium-catalyzed arylation of cyclopropenes. Journal of the American Chemical Society. 127: 3714-5. PMID 15771503 DOI: 10.1021/Ja042380K |
0.816 |
|
| 2004 |
Schwier T, Rubin M, Gevorgyan V. B(C6F5)3-catalyzed allylation of propargyl acetates with allylsilanes. Organic Letters. 6: 1999-2001. PMID 15176803 DOI: 10.1021/Ol0494055 |
0.815 |
|
| 2004 |
Rubina M, Rubin M, Gevorgyan V. Catalytic enantioselective hydrostannation of cyclopropenes. Journal of the American Chemical Society. 126: 3688-9. PMID 15038702 DOI: 10.1021/Ja0496928 |
0.791 |
|
| 2004 |
Andreev AA, Konshin VV, Komarov NV, Rubin M, Brouwer C, Gevorgyan V. Direct electrophilic silylation of terminal alkynes. Organic Letters. 6: 421-4. PMID 14748608 DOI: 10.1021/Ol036328P |
0.724 |
|
| 2004 |
Rubin M, Gevorgyan V. Simple large-scale preparation of 3,3-disubstituted cyclopropenes: Easy access to stereodefined cyclopropylmetals via transition metal-catalyzed hydrometalation Synthesis. 796-800. DOI: 10.1055/S-2003-44368 |
0.709 |
|
| 2003 |
Rubin M, Markov J, Chuprakov S, Wink DJ, Gevorgyan V. Highly regiocontrolled Pd-catalyzed cross-coupling reaction of terminal alkynes and allenylphosphine oxides. The Journal of Organic Chemistry. 68: 6251-6. PMID 12895057 DOI: 10.1021/Jo034486O |
0.794 |
|
| 2003 |
Rubina M, Rubin M, Gevorgyan V. Catalytic enantioselective hydroboration of cyclopropenes. Journal of the American Chemical Society. 125: 7198-9. PMID 12797792 DOI: 10.1021/Ja034210Y |
0.802 |
|
| 2003 |
Rubin M, Sromek AW, Gevorgyan V. New Advances in Selected Transition Metal-Catalyzed Annulations Synlett. 2265-2291. DOI: 10.1055/S-2003-43334 |
0.795 |
|
| 2002 |
Lewis FD, Zuo X, Gevorgyan V, Rubin M. Symmetry-enforced conformational control of photochemical reactivity in 2-vinyl-1,3-terphenyl. Journal of the American Chemical Society. 124: 13664-5. PMID 12431082 DOI: 10.1021/Ja028251Q |
0.641 |
|
| 2002 |
Rubina M, Rubin M, Gevorgyan V. Transition metal-catalyzed hydro-, sila-, and stannastannation of cyclopropenes: stereo- and regioselective approach toward multisubstituted cyclopropyl synthons. Journal of the American Chemical Society. 124: 11566-7. PMID 12296700 DOI: 10.1021/Ja027095K |
0.801 |
|
| 2002 |
Rubin M, Schwier T, Gevorgyan V. Highly efficient B(C(6)F(5))(3)-catalyzed hydrosilylation of olefins. The Journal of Organic Chemistry. 67: 1936-40. PMID 11895414 DOI: 10.1021/Jo016279Z |
0.809 |
|
| 2001 |
Rubin M, Gevorgyan V. B(C6F5)3-catalyzed allylation of secondary benzyl acetates with allylsilanes. Organic Letters. 3: 2705-7. PMID 11506614 DOI: 10.1021/Ol016300I |
0.707 |
|
| 2001 |
Gevorgyan V, Radhakrishnan U, Takeda A, Rubina M, Rubin M, Yamamoto Y. Palladium-catalyzed highly chemo- and regioselective formal [2+2+2] sequential cycloaddition of alkynes: a renaissance of the well known trimerization reaction? The Journal of Organic Chemistry. 66: 2835-41. PMID 11304209 DOI: 10.1021/Jo0100392 |
0.807 |
|
| 2001 |
Gevorgyan V, Rubin M, Liu JX, Yamamoto Y. A direct reduction of aliphatic aldehyde, acyl chloride, ester, and carboxylic functions into a methyl group. The Journal of Organic Chemistry. 66: 1672-5. PMID 11262111 DOI: 10.1021/Jo001258A |
0.714 |
|
| 2000 |
Gevorgyan V, Rubin M, Benson S, Liu JX, Yamamoto Y. A novel B(C(6)F(5))(3)-catalyzed reduction of alcohols and cleavage of aryl and alkyl ethers with hydrosilanes The Journal of Organic Chemistry. 65: 6179-86. PMID 10987957 DOI: 10.1021/Jo000726D |
0.716 |
|
| 2000 |
Gevorgyan V, Rubin M, Benson S, Liu JX, Yamamoto Y. A novel B(C6F5)3-catalyzed reduction of alcohols and cleavage of aryl and alkyl ethers with hydrosilanes Journal of Organic Chemistry. 65: 6179-6186. DOI: 10.1021/jo000726d |
0.657 |
|
| 1999 |
Gevorgyan V, Liu J, Rubin M, Benson S, Yamamoto Y. A novel reduction of alcohols and ethers with a HSiEt3catalytic B(C6F5)3 system Tetrahedron Letters. 40: 8919-8922. DOI: 10.1016/S0040-4039(99)01757-8 |
0.693 |
|
| 1999 |
Gevorgyan V, Liu JX, Rubin M, Benson S, Yamamoto Y. A novel reduction of alcohols and ethers with a HSiEt3/catalytic B(C6F5)3 system Tetrahedron Letters. 40: 8919-8922. |
0.617 |
|
| 1996 |
Dulayymi JRA, Baird MS, Bolesov IG, Tveresovsky V, Rubin M. A simple and efficient hydrodehalogenation of 1,1-dihalocyclopropanes Tetrahedron Letters. 37: 8933-8936. DOI: 10.1016/S0040-4039(96)02051-5 |
0.462 |
|
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