| Year |
Citation |
Score |
| 2024 |
Du Y, Mei H, Makarem A, Javahershenas R, Soloshonok VA, Han J. Copper-catalyzed multicomponent reaction of β-trifluoromethyl β-diazo esters enabling the synthesis of β-trifluoromethyl ,-diacyl-β-amino esters. Beilstein Journal of Organic Chemistry. 20: 212-219. PMID 38318462 DOI: 10.3762/bjoc.20.21 |
0.321 |
|
| 2023 |
Yao X, Li Z, Mei H, Escorihuela J, Soloshonok VA, Han J. Cascade Detrifluoroacetylation, C-S Bond Cleavage, and S2' Reaction of α,α-Difluorinated -Diols with MBH Esters. The Journal of Organic Chemistry. 88: 13057-13066. PMID 37647282 DOI: 10.1021/acs.joc.3c01220 |
0.301 |
|
| 2023 |
Vera S, Landa A, Mielgo A, Ganboa I, Oiarbide M, Soloshonok V. Catalytic Asymmetric α-Functionalization of α-Branched Aldehydes. Molecules (Basel, Switzerland). 28. PMID 36985666 DOI: 10.3390/molecules28062694 |
0.313 |
|
| 2023 |
Zhu H, Wang J, Lu Y, Soloshonok VA, Lan L, Xu J, Liu H. Pd(II) Complexes of Chiral Proline-Derived Ligands: Application for Dynamic Thermodynamic Resolution of α-Amino Acids and Their Antibacterial Activities. The Journal of Organic Chemistry. PMID 36867436 DOI: 10.1021/acs.joc.3c00008 |
0.375 |
|
| 2022 |
Wang Q, Han J, Sorochinsky A, Landa A, Butler G, Soloshonok VA. The Latest FDA-Approved Pharmaceuticals Containing Fragments of Tailor-Made Amino Acids and Fluorine. Pharmaceuticals (Basel, Switzerland). 15. PMID 36015147 DOI: 10.3390/ph15080999 |
0.304 |
|
| 2021 |
Li Z, Wang N, Liu J, Mei H, Soloshonok VA, Han J. Synthesis of Isothiazoles through -Propargylsulfinylamide: TFA-Promoted Sulfinyl Group-Involved Intramolecular Cyclization. Organic Letters. PMID 34423993 DOI: 10.1021/acs.orglett.1c02538 |
0.303 |
|
| 2021 |
Nagaoka K, Nakano A, Han J, Sakamoto T, Konno H, Moriwaki H, Abe H, Izawa K, Soloshonok VA. Comparative study of different chiral ligands for dynamic kinetic resolution of amino acids. Chirality. PMID 34402557 DOI: 10.1002/chir.23350 |
0.383 |
|
| 2020 |
Shigeno Y, Han J, Soloshonok VA, Moriwaki H, Fujiwara W, Konno H. Asymmetric synthesis of (S)-3-methyleneglutamic acid and its N-Fmoc derivative via Michael addition-elimination reaction of chiral glycine Ni (II) complex with enol tosylates. Chirality. PMID 33368628 DOI: 10.1002/chir.23291 |
0.497 |
|
| 2020 |
Fu B, Takeda R, Zou Y, Konno H, Moriwaki H, Abe H, Han J, Izawa K, Soloshonok VA. Asymmetric synthesis of (S)-α-(octyl)glycine via alkylation of Ni(II) complex of chiral glycine Schiff base. Chirality. 32: 1354-1360. PMID 33217049 DOI: 10.1002/chir.23281 |
0.503 |
|
| 2020 |
Liu J, Han J, Izawa K, Sato T, White S, Meanwell NA, Soloshonok VA. Cyclic tailor-made amino acids in the design of modern pharmaceuticals. European Journal of Medicinal Chemistry. 208: 112736. PMID 32966895 DOI: 10.1016/J.Ejmech.2020.112736 |
0.349 |
|
| 2020 |
Yin Z, Hu W, Zhang W, Konno H, Moriwaki H, Izawa K, Han J, Soloshonok VA. Tailor-made amino acid-derived pharmaceuticals approved by the FDA in 2019. Amino Acids. PMID 32880009 DOI: 10.1007/S00726-020-02887-4 |
0.385 |
|
| 2020 |
Levitskiy OA, Aglamazova OI, Grishin YK, Paseshnichenko KA, Soloshonok VA, Moriwaki H, Magdesieva TV. Solvent-triggered stereoselectivity of α,α-cyclopropanation of amino acids in the Ni(ii) chiral coordination environment. Dalton Transactions (Cambridge, England : 2003). 49: 8636-8644. PMID 32598408 DOI: 10.1039/D0Dt01578D |
0.516 |
|
| 2020 |
Zou Y, Han J, Saghyan AS, Mkrtchyan AF, Konno H, Moriwaki H, Izawa K, Soloshonok VA. Asymmetric Synthesis of Tailor-Made Amino Acids Using Chiral Ni(II) Complexes of Schiff Bases. An Update of the Recent Literature. Molecules (Basel, Switzerland). 25. PMID 32545684 DOI: 10.3390/Molecules25122739 |
0.534 |
|
| 2020 |
Han J, Butler G, Moriwaki H, Konno H, Soloshonok VA, Kitamura T. Kitamura Electrophilic Fluorination Using HF as a Source of Fluorine. Molecules (Basel, Switzerland). 25. PMID 32366048 DOI: 10.3390/molecules25092116 |
0.312 |
|
| 2020 |
Mei H, Han J, White S, Graham DJ, Izawa K, Sato T, Fustero S, Meanwell NA, Soloshonok VA. Tailor-Made Amino Acids and Fluorinated Motifs as Prominent Traits in the Modern Pharmaceuticals. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32359086 DOI: 10.1002/Chem.202000617 |
0.449 |
|
| 2020 |
Magdesieva T, Levitskiy OA, Aglamazova OI, Soloshonok VA, Moriwaki H. Which stereoinductor is better for asymmetric functionalization of α-amino acids in Ni(II) coordination environment: experimental and DFT consideration. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32187746 DOI: 10.1002/Chem.201905708 |
0.489 |
|
| 2020 |
Nagaoka K, Mei H, Guo Y, Han J, Konno H, Moriwaki H, Soloshonok VA. Michael addition reactions of chiral glycine Schiff base Ni (II)-complex with 1-(1-phenylsulfonyl)benzene. Chirality. PMID 32092199 DOI: 10.1002/Chir.23203 |
0.409 |
|
| 2020 |
Tokairin Y, Shigeno Y, Han J, Röschenthaler GV, Konno H, Moriwaki H, Soloshonok VA. Asymmetric Synthesis of 4,4-(Difluoro)glutamic Acid via Chiral Ni(II)-Complexes of Dehydroalanine Schiff Bases. Effect of the Chiral Ligands Structure on the Stereochemical Outcome. Chemistryopen. 9: 93-96. PMID 32015956 DOI: 10.1002/Open.201900343 |
0.487 |
|
| 2020 |
Wang L, Li Z, Liu J, Han J, Moriwaki H, Soloshonok VA. Recent Developments in the Asymmetric Detrifluoroacetylative Reactions of in situ Generated Mono-Fluorinated Enolates. Current Organic Chemistry. 24. DOI: 10.2174/1385272824999200801022712 |
0.365 |
|
| 2020 |
Romoff TT, Ignacio BG, Mansour N, Palmer AB, Creighton CJ, Abe H, Moriwaki H, Han J, Konno H, Soloshonok VA. Large-Scale Synthesis of the Glycine Schiff Base Ni(II) Complex Derived from (S)- and (R)-N-(2-Benzoyl-4-chlorophenyl)-1-[(3,4-dichlorophenyl)methyl]-2-pyrrolidinecarboxamide Organic Process Research & Development. 24: 294-300. DOI: 10.1021/Acs.Oprd.9B00399 |
0.492 |
|
| 2020 |
Mei H, Remete AM, Zou Y, Moriwaki H, Fustero S, Kiss L, Soloshonok VA, Han J. Fluorine-containing drugs approved by the FDA in 2019 Chinese Chemical Letters. DOI: 10.1016/J.Cclet.2020.03.050 |
0.35 |
|
| 2020 |
Oyama K, Han J, Moriwaki H, Soloshonok VA, Konno H. Synthesis of Ahod Moiety of Ralstonin A Using Amino Acid Schiff Base Ni(II)‐Complex Chemistry Helvetica Chimica Acta. 103. DOI: 10.1002/Hlca.202000077 |
0.478 |
|
| 2020 |
Llobat A, Escorihuela J, Sedgwick DM, Rodenes M, Román R, Soloshonok VA, Han J, Medio-Simón M, Fustero S. The Ruthenium-Catalyzed Domino Cross Enyne Metathesis/Ring-Closing Metathesis in the Synthesis of Enantioenriched Nitrogen-Containing Heterocycles European Journal of Organic Chemistry. 2020: 4193-4207. DOI: 10.1002/Ejoc.202000598 |
0.375 |
|
| 2020 |
Mei H, Han J, White S, Graham DJ, Izawa K, Sato T, Fustero S, Meanwell NA, Soloshonok VA. Frontispiece: Tailor‐Made Amino Acids and Fluorinated Motifs as Prominent Traits in Modern Pharmaceuticals Chemistry: a European Journal. 26. DOI: 10.1002/Chem.202085061 |
0.426 |
|
| 2020 |
Llobat A, Sedgwick DM, Cabré A, Román R, Mateu N, Escorihuela J, Medio‐Simón M, Soloshonok V, Han J, Riera A, Fustero S. Asymmetric Synthesis of Fluorinated Monoterpenic Alkaloid Derivatives from Chiral Fluoroalkyl Aldimines via the Pauson‐Khand Reaction Advanced Synthesis & Catalysis. 362: 1378-1384. DOI: 10.1002/Adsc.201901504 |
0.458 |
|
| 2019 |
Han J, Takeda R, Liu X, Konno H, Abe H, Hiramatsu T, Moriwaki H, Soloshonok VA. Preparative Method for Asymmetric Synthesis of ()-2-Amino-4,4,4-trifluorobutanoic Acid. Molecules (Basel, Switzerland). 24. PMID 31835583 DOI: 10.3390/Molecules24244521 |
0.521 |
|
| 2019 |
Han J, Romoff TT, Moriwaki H, Konno H, Soloshonok VA. Development of Hamari Ligands for Practical Asymmetric Synthesis of Tailor-Made Amino Acids. Acs Omega. 4: 18942-18947. PMID 31763515 DOI: 10.1021/acsomega.9b02940 |
0.442 |
|
| 2019 |
Mei H, Han J, Klika KD, Izawa K, Sato T, Meanwell NA, Soloshonok VA. Applications of fluorine-containing amino acids for drug design. European Journal of Medicinal Chemistry. 111826. PMID 31740056 DOI: 10.1016/J.Ejmech.2019.111826 |
0.414 |
|
| 2019 |
Kwiatkowska M, Marcinkowska M, Wzorek A, Pajkert R, Han J, Klika KD, Soloshonok VA, Röschenthaler GV. The self-disproportionation of enantiomers (SDE) via column chromatography of β-amino-α,α-difluorophosphonic acid derivatives. Amino Acids. PMID 31468209 DOI: 10.1007/S00726-019-02774-7 |
0.481 |
|
| 2019 |
Mei H, Han J, Takeda R, Sakamoto T, Miwa T, Minamitsuji Y, Moriwaki H, Abe H, Soloshonok VA. Practical Method for Preparation of ()-2-Amino-5,5,5-trifluoropentanoic Acid via Dynamic Kinetic Resolution. Acs Omega. 4: 11844-11851. PMID 31460294 DOI: 10.1021/acsomega.9b01537 |
0.338 |
|
| 2019 |
Yin Z, Moriwaki H, Abe H, Miwa T, Han J, Soloshonok VA. Large-Scale Asymmetric Synthesis of Fmoc-()-2-Amino-6,6,6-Trifluorohexanoic Acid. Chemistryopen. 8: 701-704. PMID 31183311 DOI: 10.1002/Open.201900131 |
0.483 |
|
| 2019 |
Han J, Takeda R, Sato T, Moriwaki H, Abe H, Izawa K, Soloshonok VA. Optical Resolution of Rimantadine. Molecules (Basel, Switzerland). 24. PMID 31083636 DOI: 10.3390/Molecules24091828 |
0.387 |
|
| 2019 |
Mei H, Jean M, Albalat M, Vanthuyne N, Roussel C, Moriwaki H, Yin Z, Han J, Soloshonok VA. Effect of substituents on the configurational stability of the stereogenic nitrogen in metal(II) complexes of α-amino acid Schiff bases. Chirality. PMID 30916841 DOI: 10.1002/Chir.23066 |
0.456 |
|
| 2019 |
Han J, Wzorek A, Kwiatkowska M, Soloshonok VA, Klika KD. The self-disproportionation of enantiomers (SDE) of amino acids and their derivatives. Amino Acids. PMID 30903285 DOI: 10.1007/S00726-019-02729-Y |
0.421 |
|
| 2019 |
Han J, Jean M, Roussel C, Moriwaki H, Soloshonok VA. Chromatographic approach to study the configurational stability of Ni(II) complexes of amino-acid Schiff bases possessing stereogenic nitrogen. Chirality. PMID 30702773 DOI: 10.1002/Chir.23059 |
0.392 |
|
| 2019 |
Han J, Wzorek A, Soloshonok VA, Klika KD. The self-disproportionation of enantiomers (SDE): the effect of scaling down, potential problems vs. prospective applications, possible new occurrences, and unrealized opportunities? Electrophoresis. PMID 30653701 DOI: 10.1002/Elps.201800414 |
0.326 |
|
| 2019 |
Mei H, Yin Z, Miwa T, Moriwaki H, Abe H, Han J, Soloshonok VA. Convenient Asymmetric Synthesis of Fmoc-(S)-6,6,6-Trifluoro-Norleucine Symmetry. 11: 578. DOI: 10.3390/Sym11040578 |
0.521 |
|
| 2019 |
Imai T, Niijima E, Terada S, Wzorek A, Soloshonok VA, Hori A, Kitagawa O. Chirality-dependent halogen bonds in axially chiral quinazolin-4-one derivatives bearing ortho-halophenyl groups Crystengcomm. 21: 3385-3389. DOI: 10.1039/C9Ce00320G |
0.327 |
|
| 2019 |
Takahashi M, Moriwaki H, Miwa T, Hoang B, Wang P, Soloshonok VA. Large Scale Synthesis of Chiral (3Z,5Z)-2,7-Dihydro-1H-azepine-Derived Hamari Ligand for General Asymmetric Synthesis of Tailor-Made Amino Acids Organic Process Research & Development. 23: 619-628. DOI: 10.1021/Acs.Oprd.8B00406 |
0.505 |
|
| 2019 |
Mei H, Hiramatsu T, Takeda R, Moriwaki H, Abe H, Han J, Soloshonok VA. Expedient Asymmetric Synthesis of (S)-2-Amino-4,4,4-trifluorobutanoic Acid via Alkylation of Chiral Nucleophilic Glycine Equivalent Organic Process Research & Development. 23: 629-634. DOI: 10.1021/Acs.Oprd.8B00404 |
0.525 |
|
| 2019 |
Tokairin Y, Soloshonok VA, Konno H, Moriwaki H, Röschenthaler G. Convenient synthesis of racemic 4,4-difluoro glutamic acid derivatives via Michael-type additions of Ni(II)-complex of dehydroalanine Schiff bases Journal of Fluorine Chemistry. 227: 109376. DOI: 10.1016/J.Jfluchem.2019.109376 |
0.505 |
|
| 2019 |
Mei H, Han J, White S, Butler G, Soloshonok VA. Perfluoro-3-ethyl-2,4-dimethyl-3-pentyl persistent radical: A new reagent for direct, metal-free radical trifluoromethylation and polymer initiation Journal of Fluorine Chemistry. 227: 109370. DOI: 10.1016/J.Jfluchem.2019.109370 |
0.309 |
|
| 2019 |
Zhu Y, Ni Y, Soloshonok VA, Han J, Pan Y. Catalytic enantioselective Michael addition reactions between in situ detrifluoroacetylatively generated 3-fluorooxindole-derived enolates and 1-(1-(phenylsulfonyl)vinylsulfonyl)benzene Journal of Fluorine Chemistry. 219: 32-38. DOI: 10.1016/J.Jfluchem.2018.12.009 |
0.406 |
|
| 2019 |
Fustero S, Rodenes M, Román R, Sedgwick DM, Aguado JE, Soloshonok VA, Han J, Mei H, Medio‐Simon M, Barrio P. Asymmetric Vinylogous Mukaiyama‐Mannich Reactions of Heterocyclic Siloxy Dienes with Ellman's Fluorinated Aldimines Advanced Synthesis & Catalysis. 361: 3860-3867. DOI: 10.1002/Adsc.201900464 |
0.372 |
|
| 2018 |
Takeda R, Kawashima A, Yamamoto J, Sato T, Moriwaki H, Izawa K, Abe H, Soloshonok VA. Tandem Alkylation-Second-Order Asymmetric Transformation Protocol for the Preparation of Phenylalanine-Type Tailor-Made α-Amino Acids. Acs Omega. 3: 9729-9737. PMID 31459102 DOI: 10.1021/acsomega.8b01424 |
0.419 |
|
| 2018 |
Mei H, Liu J, Fustero S, Román R, Ruzziconi R, Soloshonok VA, Han J. Chemistry of detrifluoroacetylatively in situ generated fluoro-enolates. Organic & Biomolecular Chemistry. PMID 30574988 DOI: 10.1039/C8Ob02843E |
0.37 |
|
| 2018 |
Tokairin Y, Soloshonok VA, Moriwaki H, Konno H. Asymmetric synthesis of (2S,3S)-3-Me-glutamine and (R)-allo-threonine derivatives proper for solid-phase peptide coupling. Amino Acids. PMID 30449004 DOI: 10.1007/S00726-018-2677-5 |
0.42 |
|
| 2018 |
Mazzeo G, Longhi G, Abbate S, Mangiavacchi F, Santi C, Han J, Soloshonok VA, Melensi L, Ruzziconi R. Mannich-type addition of 1,3-dicarbonyl compounds to chiral tert-butanesulfinyltrifluoroacetaldimines. Mechanistic aspects and chiroptical studies. Organic & Biomolecular Chemistry. PMID 30393798 DOI: 10.1039/C8Ob02204F |
0.36 |
|
| 2018 |
Hosaka T, Imai T, Wzorek A, Marcinkowska M, Kolbus A, Kitagawa O, Soloshonok VA, Klika KD. The self-disproportionation of enantiomers (SDE) of α-amino acid derivatives: facets of steric and electronic properties. Amino Acids. PMID 30311082 DOI: 10.1007/S00726-018-2664-X |
0.467 |
|
| 2018 |
Klika KD, Wzorek A, Soloshonok VA. Internal chirality descriptors iR and iS and ire and isi. A proposed notation to extend the usefulness of the R/S system by retaining the sense of stereochemistry in cases of ligand ranking changes. Chirality. PMID 29978505 DOI: 10.1002/Chir.22982 |
0.342 |
|
| 2018 |
Takeda R, Kawamura A, Kawashima A, Sato T, Moriwaki H, Izawa K, Abe H, Soloshonok VA. Second-order asymmetric transformation and its application for the practical synthesis of α-amino acids. Organic & Biomolecular Chemistry. PMID 29947401 DOI: 10.1039/C8Ob00963E |
0.52 |
|
| 2018 |
Zhu Y, Mao Y, Mei H, Pan Y, Han J, Soloshonok VA, Hayashi T. Palladium-Catalyzed Asymmetric Allylic Alkylations of Colby Pro-Enolates with MBH Carbonates: Enantioselective Access to Quaternary C-F Oxindoles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29683211 DOI: 10.1002/Chem.201801670 |
0.381 |
|
| 2018 |
Han J, Kitagawa O, Wzorek A, Klika KD, Soloshonok VA. The self-disproportionation of enantiomers (SDE): a menace or an opportunity? Chemical Science. 9: 1718-1739. PMID 29675218 DOI: 10.1039/C7Sc05138G |
0.358 |
|
| 2018 |
Zhang W, Ekomo RE, Roussel C, Moriwaki H, Abe H, Han J, Soloshonok VA. Axially chiral Ni(II) complexes of α-amino acids: Separation of enantiomers and kinetics of racemization. Chirality. PMID 29359493 DOI: 10.1002/Chir.22815 |
0.55 |
|
| 2018 |
Mei H, Han J, Fustero S, Román R, Ruzziconi R, Soloshonok VA. Recent progress in the application of fluorinated chiral sulfinimine reagents Journal of Fluorine Chemistry. 216: 57-70. DOI: 10.1016/J.Jfluchem.2018.10.003 |
0.456 |
|
| 2018 |
Hao J, Milcent T, Retailleau P, Soloshonok VA, Ongeri S, Crousse B. Asymmetric Synthesis of Cyclic Fluorinated Amino Acids European Journal of Organic Chemistry. 2018: 3688-3692. DOI: 10.1002/Ejoc.201800255 |
0.506 |
|
| 2018 |
Zhou S, Wang S, Wang J, Nian Y, Peng P, Soloshonok VA, Liu H. Configurationally Stable (S
)- and (R
)-α-Methylproline-Derived Ligands for the Direct Chemical Resolution of Free Unprotected β3
-Amino Acids European Journal of Organic Chemistry. 2018: 1821-1832. DOI: 10.1002/Ejoc.201800120 |
0.477 |
|
| 2018 |
Sanz-Vidal Á, Torres J, Soloshonok VA, Zhu Y, Han J, Fustero S, del Pozo C. Asymmetric Vinylogous Mannich-Type Addition of α,α-Dicyanoalkenes to α-Fluoroalkyl Sulfinyl Imines Advanced Synthesis & Catalysis. 360: 366-373. DOI: 10.1002/Adsc.201701284 |
0.46 |
|
| 2017 |
Han J, Soloshonok VA, Klika KD, Drabowicz J, Wzorek A. Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome. Chemical Society Reviews. PMID 29271432 DOI: 10.1039/C6Cs00703A |
0.411 |
|
| 2017 |
Takeda R, Abe H, Shibata N, Moriwaki H, Izawa K, Soloshonok VA. Asymmetric synthesis of α-deuterated α-amino acids. Organic & Biomolecular Chemistry. PMID 28792052 DOI: 10.1039/C7Ob01720K |
0.542 |
|
| 2017 |
Wang S, Zhou S, Wang J, Nian Y, Kawashima A, Moriwaki H, Aceña JL, Soloshonok VA, Liu H. Correction to "Chemical Dynamic Thermodynamic Resolution and S/R Interconversion of Unprotected Unnatural Tailor-made α-Amino Acids". The Journal of Organic Chemistry. PMID 28718643 DOI: 10.1021/Acs.Joc.7B01660 |
0.445 |
|
| 2017 |
Wang Y, Song X, Wang J, Moriwaki H, Soloshonok VA, Liu H. Recent approaches for asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes. Amino Acids. PMID 28674862 DOI: 10.1007/S00726-017-2458-6 |
0.535 |
|
| 2017 |
Zhu Y, Zhang W, Mei H, Han J, Soloshonok VA, Pan Y. Catalytic Enantioselective Michael Addition Reactions of Detrifluoroacetylatively Generated Tertiary Enolates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28639718 DOI: 10.1002/Chem.201702091 |
0.42 |
|
| 2017 |
Matsuoka M, Goto M, Wzorek A, Soloshonok VA, Kitagawa O. Diastereoselective α-Alkylation of Metallo Enamines Generated from N-C Axially Chiral Mebroqualone Derivatives. Organic Letters. PMID 28459589 DOI: 10.1021/Acs.Orglett.7B00998 |
0.46 |
|
| 2017 |
Mazzeo G, Longhi G, Abbate S, Palomba M, Bagnoli L, Marini F, Santi C, Han J, Soloshonok VA, Di Crescenzo E, Ruzziconi R. Solvent-free, uncatalyzed asymmetric "ene" reactions of N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimines: a general approach to enantiomerically pure α-(trifluoromethyl)tryptamines. Organic & Biomolecular Chemistry. PMID 28436530 DOI: 10.1039/C7Ob00670E |
0.484 |
|
| 2017 |
Nian Y, Wang J, Moriwaki H, Soloshonok VA, Liu H. Analysis of crystallographic structures of Ni(ii) complexes of α-amino acid Schiff bases: elucidation of the substituent effect on stereochemical preferences. Dalton Transactions (Cambridge, England : 2003). PMID 28287668 DOI: 10.1039/C7Dt00014F |
0.535 |
|
| 2017 |
Nishimine T, Taira H, Mori S, Matsubara O, Tokunaga E, Akiyama H, Soloshonok VA, Shibata N. Synthesis of chiral (tetrazolyl)methyl-containing acrylates via silicon-induced organocatalytic kinetic resolution of Morita-Baylis-Hillman fluorides. Chemical Communications (Cambridge, England). PMID 28054095 DOI: 10.1039/C6Cc08830A |
0.332 |
|
| 2017 |
Drabowicz J, Jasiak A, Wzorek A, Sato A, Soloshonok VA. Self-disproportionation of enantiomers (SDE) of chiral sulfur-containing compounds via achiral chromatography Arkivoc. 2017: 557-578. DOI: 10.24820/Ark.5550190.P009.829 |
0.313 |
|
| 2017 |
Xie C, Sha W, Zhu Y, Han J, Soloshonok VA, Pan Y. Asymmetric synthesis of C–F quaternary α-fluoro-β-amino-indolin-2-ones via Mannich addition reactions; facets of reactivity, structural generality and stereochemical outcome Rsc Advances. 7: 5679-5683. DOI: 10.1039/C6Ra27710A |
0.485 |
|
| 2017 |
Romoff TT, Palmer AB, Mansour N, Creighton CJ, Miwa T, Ejima Y, Moriwaki H, Soloshonok VA. Scale-up Synthesis of (R)- and (S)-N-(2-Benzoyl-4-chlorophenyl)-1-(3,4-dichlorobenzyl)pyrrolidine-2-carboxamide Hydrochloride, A Versatile Reagent for the Preparation of Tailor-Made α- and β-Amino Acids in an Enantiomerically Pure Form Organic Process Research & Development. 21: 732-739. DOI: 10.1021/Acs.Oprd.7B00055 |
0.53 |
|
| 2017 |
Soloshonok VA, Wzorek A, Klika KD. A question of policy: should tests for the self-disproportionation of enantiomers (SDE) be mandatory for reports involving scalemates? Tetrahedron: Asymmetry. 28: 1430-1434. DOI: 10.1016/J.Tetasy.2017.08.020 |
0.306 |
|
| 2017 |
Zhu Y, Zhang W, Mei H, Han J, Soloshonok VA, Pan Y. Unusual reactivity of fluoro-enolates with dialkyl azodicarboxylates: Synthesis of isatin-hydrazones Journal of Fluorine Chemistry. 203: 99-103. DOI: 10.1016/J.Jfluchem.2017.06.010 |
0.41 |
|
| 2017 |
Zhang L, Zhang W, Sha W, Mei H, Han J, Soloshonok VA. Detrifluoroacetylative generation and chemistry of fluorine containing tertiary enolates Journal of Fluorine Chemistry. 198: 2-9. DOI: 10.1016/J.Jfluchem.2016.12.007 |
0.362 |
|
| 2017 |
Wzorek A, Kamizela A, Sato A, Soloshonok VA. Self-Disproportionation of Enantiomers (SDE) via achiral gravity-driven column chromatography of N -fluoroacyl-1-phenylethylamines Journal of Fluorine Chemistry. 196: 37-43. DOI: 10.1016/J.Jfluchem.2016.07.016 |
0.326 |
|
| 2017 |
Sha W, Zhang L, Wu X, Mei H, Han J, Soloshonok VA, Pan Y. Detrifluoroacetylative cascade reactions of bicyclic fluoro-enolates with ortho -phthalaldehyde: Aspects of reactivity, diastereo- and enantioselectivity Journal of Fluorine Chemistry. 196: 14-23. DOI: 10.1016/J.Jfluchem.2016.06.008 |
0.415 |
|
| 2017 |
Zhang W, Sha W, Pajkert R, Mei H, Pan Y, Han J, Röschenthaler G, Soloshonok VA. β-Amino-γ,γ-difluoro-ω-phosphonoglutamic Acid Derivatives: An Unexplored, Multifaceted Structural Type of Tailor-Made α-Amino Acids European Journal of Organic Chemistry. 2017: 3451-3456. DOI: 10.1002/EJOC.201700570 |
0.378 |
|
| 2017 |
Bremerich M, Bolm C, Raabe G, Soloshonok VA. Design, Synthesis, and Evaluation of N
-(tert
-Butyl)-Alanine-Derived Chiral Ligands - Aspects of Reactivity and Diastereoselectivity in the Reactions with α-Amino Acids European Journal of Organic Chemistry. 2017: 3211-3221. DOI: 10.1002/Ejoc.201700339 |
0.559 |
|
| 2017 |
Yamamoto J, Kawashima A, Kawamura A, Abe H, Moriwaki H, Shibata N, Soloshonok VA. Operationally Convenient and Scalable Asymmetric Synthesis of (2S
)- and (2R
)-α-(Methyl)cysteine Derivatives through Alkylation of Chiral Alanine Schiff Base NiII
Complexes European Journal of Organic Chemistry. 2017: 1931-1939. DOI: 10.1002/Ejoc.201700018 |
0.446 |
|
| 2017 |
Zhang W, Sha W, Zhu Y, Han J, Soloshonok VA, Pan Y. Asymmetric Synthesis of Quaternary β-Perfluorophenyl-β-amino-indolin-2-ones European Journal of Organic Chemistry. 2017: 1540-1546. DOI: 10.1002/Ejoc.201601645 |
0.392 |
|
| 2017 |
Zhang W, Wang X, Zhu B, Zhu D, Han J, Wzorek A, Sato A, Soloshonok VA, Zhou J, Pan Y. Diastereoselective Regiodivergent Mannich Versus Tandem Mannich-Cyclization Reactions Advanced Synthesis & Catalysis. 359: 4267-4273. DOI: 10.1002/Adsc.201701066 |
0.348 |
|
| 2016 |
Zhang L, Zhang W, Mei H, Han J, Soloshonok VA, Pan Y. Catalytic asymmetric aldol addition reactions of 3-fluoro-indolinone derived enolates. Organic & Biomolecular Chemistry. PMID 27910989 DOI: 10.1039/C6Ob02454H |
0.486 |
|
| 2016 |
Sha W, Zhang L, Zhang W, Mei H, Soloshonok VA, Han J, Pan Y. Catalytic cascade aldol-cyclization of tertiary ketone enolates for enantioselective synthesis of keto-esters with a C-F quaternary stereogenic center. Organic & Biomolecular Chemistry. PMID 27397559 DOI: 10.1039/c6ob01152g |
0.374 |
|
| 2016 |
Xie C, Zhang L, Sha W, Soloshonok VA, Han J, Pan Y. Detrifluoroacetylative in Situ Generation of Free 3-Fluoroindolin-2-one-Derived Tertiary Enolates: Design, Synthesis, and Assessment of Reactivity toward Asymmetric Mannich Reactions. Organic Letters. PMID 27305459 DOI: 10.1021/acs.orglett.6b01516 |
0.374 |
|
| 2016 |
Wzorek A, Sato A, Drabowicz J, Soloshonok VA. Self-disproportionation of enantiomers via achiral gravity-driven column chromatography: A case study of N-acyl-α-phenylethylamines. Journal of Chromatography. A. PMID 27240946 DOI: 10.1016/J.Chroma.2016.05.044 |
0.36 |
|
| 2016 |
Nian Y, Wang J, Zhou S, Dai W, Wang S, Moriwaki H, Kawashima A, Soloshonok VA, Liu H. Purely Chemical Approach for Preparation of D-alpha-amino Acids via (S)-to-(R)-interconversion of Unprotected Tailor-made alpha-amino Acids. The Journal of Organic Chemistry. PMID 27053152 DOI: 10.1021/acs.joc.5b02707 |
0.38 |
|
| 2016 |
Xie C, Zhang L, Mei H, Pajkert R, Ponomarenko M, Pan Y, Röschenthaler GV, Soloshonok VA, Han J. New Chiral Reagent for Installation of Pharmacophoric (S)- or (R)-2-(Alkoxyphosphono)-1-Amino-2,2-Difluoroethyl Group. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26952046 DOI: 10.1002/chem.201600758 |
0.345 |
|
| 2016 |
Wzorek A, Sato A, Drabowicz J, Soloshonok VA, Klika KD. Remarkable magnitude of the self-disproportionation of enantiomers (SDE) via achiral chromatography: application to the practical-scale enantiopurification of β-amino acid esters. Amino Acids. 48: 605-13. PMID 26704565 DOI: 10.1007/S00726-015-2152-5 |
0.456 |
|
| 2016 |
Goto M, Tateishi K, Ebine K, Soloshonok VA, Roussel C, Kitagawa O. Chiral additive induced self-disproportionation of enantiomers under MPLC conditions: preparation of enantiomerically pure samples of 1-(aryl)ethylamines from racemates Tetrahedron: Asymmetry. 27: 317-321. DOI: 10.1016/J.Tetasy.2016.03.004 |
0.361 |
|
| 2016 |
Wzorek A, Sato A, Drabowicz J, Soloshonok VA. Self-disproportionation of Enantiomers (SDE) of Chiral Nonracemic Amides via Achiral Chromatography Israel Journal of Chemistry. 56: 977-989. DOI: 10.1002/Ijch.201600077 |
0.46 |
|
| 2016 |
Mei H, Xie C, Han J, Soloshonok VA. N-tert-Butylsulfinyl-3,3,3-trifluoroacetaldimine: Versatile Reagent for Asymmetric Synthesis of Trifluoromethyl-Containing Amines and Amino Acids of Pharmaceutical Importance European Journal of Organic Chemistry. 2016: 5917-5932. DOI: 10.1002/Ejoc.201600578 |
0.501 |
|
| 2016 |
Sato T, Izawa K, Aceña JL, Liu H, Soloshonok VA. Tailor-Made α-Amino Acids in the Pharmaceutical Industry: Synthetic Approaches to (1R,2S)-1-Amino-2-vinylcyclopropane-1-carboxylic Acid (Vinyl-ACCA) European Journal of Organic Chemistry. 2016: 2757-2774. DOI: 10.1002/EJOC.201600112 |
0.383 |
|
| 2016 |
Sato T, Izawa K, Acena JL, Liu H, Soloshonok VA. ChemInform Abstract: Tailor-Made α-Amino Acids in the Pharmaceutical Industry: Synthetic Approaches to (1R,2S)-1-Amino-2-vinylcyclopropane-1-carboxylic Acid (Vinyl-ACCA) Cheminform. 47. DOI: 10.1002/CHIN.201635169 |
0.389 |
|
| 2016 |
Dai Y, Xie C, Mei H, Han J, Soloshonok VA, Pan Y. ChemInform Abstract: Asymmetric Synthesis of β-Trifluoromethyl-β-amino Acids, Including Highly Sterically Constrained α,α-Dialkyl Derivatives. Cheminform. 47. DOI: 10.1002/CHIN.201616070 |
0.36 |
|
| 2016 |
Xie C, Zhang L, Mei H, Pajkert R, Ponomarenko M, Pan Y, Röschenthaler G, Soloshonok VA, Han J. Inside Cover: New Chiral Reagent for Installation of Pharmacophoric (S)- or (R)-2-(Alkoxyphosphono)-1-amino-2,2-difluoroethyl Groups (Chem. Eur. J. 21/2016) Chemistry - a European Journal. 22: 6990-6990. DOI: 10.1002/Chem.201601402 |
0.38 |
|
| 2015 |
Kawashima A, Shu S, Takeda R, Kawamura A, Sato T, Moriwaki H, Wang J, Izawa K, Aceña JL, Soloshonok VA, Liu H. Advanced asymmetric synthesis of (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid by alkylation/cyclization of newly designed axially chiral Ni(II) complex of glycine Schiff base. Amino Acids. PMID 26661034 DOI: 10.1007/S00726-015-2138-3 |
0.557 |
|
| 2015 |
Li T, Zhou S, Wang J, Aceña JL, Soloshonok VA, Liu H. Asymmetric synthesis of (2S,3S)-alpha-(1-oxoisoindolin-3-yl)glycines under low-basicity "kinetic" control. The Journal of Organic Chemistry. PMID 26523334 DOI: 10.1021/acs.joc.5b01730 |
0.334 |
|
| 2015 |
Nian Y, Wang J, Zhou S, Wang S, Moriwaki H, Kawashima A, Soloshonok VA, Liu H. Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids. Angewandte Chemie (International Ed. in English). PMID 26367134 DOI: 10.1002/Anie.201507273 |
0.484 |
|
| 2015 |
Wang S, Zhou S, Wang J, Nian Y, Kawashima A, Moriwaki H, Aceña JL, Soloshonok VA, Liu H. Chemical Dynamic Thermodynamic Resolution and S/R Interconversion of Unprotected Unnatural Tailor-Made alpha-Amino Acids. The Journal of Organic Chemistry. PMID 26352915 DOI: 10.1021/Acs.Joc.5B01292 |
0.516 |
|
| 2015 |
Xie C, Dai Y, Mei H, Han J, Soloshonok VA, Pan Y. Asymmetric synthesis of quaternary α-fluoro-β-keto-amines via detrifluoroacetylative Mannich reactions. Chemical Communications (Cambridge, England). 51: 9149-52. PMID 25947253 DOI: 10.1039/c5cc02256h |
0.348 |
|
| 2015 |
Xie C, Wu L, Han J, Soloshonok VA, Pan Y. Assembly of Fluorinated Quaternary Stereogenic Centers through Catalytic Enantioselective Detrifluoroacetylative Aldol Reactions. Angewandte Chemie (International Ed. in English). 54: 6019-23. PMID 25808758 DOI: 10.1002/anie.201500908 |
0.354 |
|
| 2015 |
Sato A, Han J, Ono T, Wzorek A, Aceña JL, Soloshonok VA. Introducing a new radical trifluoromethylation reagent. Chemical Communications (Cambridge, England). 51: 5967-70. PMID 25736068 DOI: 10.1039/C5Cc00905G |
0.317 |
|
| 2015 |
Wu L, Xie C, Mei H, Dai Y, Han J, Soloshonok VA, Pan Y. Synthesis of trifluoromethyl-containing vicinal diamines by asymmetric decarboxylative mannich addition reactions. The Journal of Organic Chemistry. 80: 3187-94. PMID 25714116 DOI: 10.1021/acs.joc.5b00124 |
0.334 |
|
| 2015 |
Li T, Zhou S, Wang J, Aceña JL, Soloshonok VA, Liu H. Asymmetric synthesis of α-(1-oxoisoindolin-3-yl)glycine: Synthetic and mechanistic challenges Chemical Communications. 51: 1624-1626. PMID 25500794 DOI: 10.1039/C4Cc05659K |
0.505 |
|
| 2015 |
Dai Y, Xie C, Wu L, Mei H, Soloshonok VA, Han J, Pan Y. Asymmetric synthesis of amino-benzothiazol derivatives by additions of 2-lithiated benzothiazoles to (S)-N-t-butylsulfinyl-ketimines Rsc Advances. 5: 3491-3497. DOI: 10.1039/C4RA15405C |
0.377 |
|
| 2015 |
Suzuki Y, Han J, Kitagawa O, Aceña JL, Klika KD, Soloshonok VA. A comprehensive examination of the self-disproportionation of enantiomers (SDE) of chiral amides via achiral, laboratory-routine, gravity-driven column chromatography Rsc Advances. 5: 2988-2993. DOI: 10.1039/C4Ra13928C |
0.309 |
|
| 2015 |
Kawashima A, Xie C, Mei H, Takeda R, Kawamura A, Sato T, Moriwaki H, Izawa K, Han J, Aceña JL, Soloshonok VA. Asymmetric synthesis of (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid by sequential SN2-SN2′ dialkylation of (R)-N-(benzyl)proline-derived glycine Schiff base Ni(ii) complex Rsc Advances. 5: 1051-1058. DOI: 10.1039/C4Ra12658K |
0.494 |
|
| 2015 |
Xie C, Wu L, Zhou J, Mei H, Soloshonok VA, Han J, Pan Y. Synthesis of α,α-difluoro-β-amino carbonyl-containing sulfonamides and related compounds Journal of Fluorine Chemistry. 172: 13-21. DOI: 10.1016/J.JFLUCHEM.2015.01.004 |
0.32 |
|
| 2015 |
Kawamura A, Moriwaki H, Röschenthaler GV, Kawada K, Aceña JL, Soloshonok VA. Synthesis of (2S,3S)-β-(trifluoromethyl)-α,β-diamino acid by Mannich addition of glycine Schiff base Ni(II) complexes to N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimine Journal of Fluorine Chemistry. 171: 67-72. DOI: 10.1016/J.Jfluchem.2014.09.013 |
0.529 |
|
| 2015 |
Han J, Aceña JL, Yasuda N, Uekusa H, Ono T, Soloshonok VA, Klika KD. Carbonyl group coordination preferences in square-planar NiII and PdII complexes of pentadentate ligands by electron-withdrawing/donating substituents Inorganica Chimica Acta. 433: 3-12. DOI: 10.1016/J.Ica.2015.04.029 |
0.333 |
|
| 2015 |
Wzorek A, Sato A, Drabowicz J, Soloshonok VA, Klika KD. Enantiomeric enrichments via the self-disproportionation of enantiomers (SDE) by achiral, gravity-driven column chromatography: A case study using N-(1-phenylethyl)acetamide for optimizing the enantiomerically pure yield and magnitude of the SDE Helvetica Chimica Acta. 98: 1147-1159. DOI: 10.1002/Hlca.201500041 |
0.343 |
|
| 2015 |
Mei H, Xie C, Aceña JL, Soloshonok VA, Röschenthaler G, Han J. Recent Progress in the in situ Detrifluoroacetylative Generation of Fluoro Enolates and Their Reactions with Electrophiles European Journal of Organic Chemistry. 2015: 6401-6412. DOI: 10.1002/Ejoc.201500787 |
0.386 |
|
| 2015 |
Jörres M, Aceña JL, Soloshonok VA, Bolm C. Asymmetric Carbon-Carbon Bond Formation under Solventless Conditions in Ball Mills Chemcatchem. 7: 1265-1269. DOI: 10.1002/Cctc.201500102 |
0.455 |
|
| 2015 |
Nian Y, Wang J, Zhou S, Wang S, Moriwaki H, Kawashima A, Soloshonok VA, Liu H. Inside Cover: Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids (Angew. Chem. Int. Ed. 44/2015) Angewandte Chemie International Edition. 54: 12826-12826. DOI: 10.1002/Anie.201508520 |
0.444 |
|
| 2015 |
Nian Y, Wang J, Zhou S, Wang S, Moriwaki H, Kawashima A, Soloshonok VA, Liu H. Innentitelbild: Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids (Angew. Chem. 44/2015) Angewandte Chemie. 127: 13018-13018. DOI: 10.1002/Ange.201508520 |
0.447 |
|
| 2015 |
Dai Y, Xie C, Zhou J, Mei H, Soloshonok VA, Han J, Pan Y. Generalized Approach to Asymmetric Synthesis of β-Substituted β-Amino Acids Bearing CHF2, CBrF2, and CClF2Groups Asian Journal of Organic Chemistry. 4: 1020-1024. DOI: 10.1002/AJOC.201500252 |
0.366 |
|
| 2014 |
Takeda R, Kawamura A, Kawashima A, Sato T, Moriwaki H, Izawa K, Akaji K, Wang S, Liu H, Aceña JL, Soloshonok VA. Chemical dynamic kinetic resolution and S/R interconversion of unprotected α-amino acids. Angewandte Chemie (International Ed. in English). 53: 12214-7. PMID 25244328 DOI: 10.1002/Anie.201407944 |
0.494 |
|
| 2014 |
Qian P, Xie C, Wu L, Mei H, Soloshonok VA, Han J, Pan Y. Asymmetric synthesis of (3S,1′S)-3-(1-amino-2,2,2-trifluoroethyl)-1-(alkyl)-indolin-2-one derivatives by addition of (S)-N-t-butylsulfinyl-3,3,3-trifluoroacetaldimine to 1-(alkyl)-indolin-2-ones Organic and Biomolecular Chemistry. 12: 7909-7913. PMID 25220306 DOI: 10.1039/c4ob01453g |
0.383 |
|
| 2014 |
Xie C, Wu L, Mei H, Soloshonok VA, Han J, Pan Y. Generalized access to fluorinated β-keto amino compounds through asymmetric additions of α,α-difluoroenolates to CF3-sulfinylimine. Organic & Biomolecular Chemistry. 12: 7836-43. PMID 25167342 DOI: 10.1039/c4ob01575d |
0.36 |
|
| 2014 |
Wu L, Xie C, Mei H, Soloshonok VA, Han J, Pan Y. Asymmetric Friedel-Crafts reactions of N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimines: general access to enantiomerically pure indoles containing a 1-amino-2,2,2-trifluoroethyl group. The Journal of Organic Chemistry. 79: 7677-81. PMID 25051149 DOI: 10.1021/Jo5012009 |
0.438 |
|
| 2014 |
Takeda R, Kawamura A, Kawashima A, Moriwaki H, Sato T, Aceña JL, Soloshonok VA. Design and synthesis of (S)- and (R)-α-(phenyl)ethylamine-derived NH-type ligands and their application for the chemical resolution of α-amino acids. Organic & Biomolecular Chemistry. 12: 6239-49. PMID 25008025 DOI: 10.1039/C4Ob00669K |
0.515 |
|
| 2014 |
Zhou S, Wang J, Chen X, Aceña JL, Soloshonok VA, Liu H. Chemical kinetic resolution of unprotected β-substituted β-amino acids using recyclable chiral ligands. Angewandte Chemie (International Ed. in English). 53: 7883-6. PMID 24917560 DOI: 10.1002/Anie.201403556 |
0.483 |
|
| 2014 |
Aceña JL, Sorochinsky AE, Soloshonok V. Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 3: Michael addition reactions and miscellaneous transformations. Amino Acids. 46: 2047-73. PMID 24888480 DOI: 10.1007/s00726-014-1764-5 |
0.398 |
|
| 2014 |
Wzorek A, Klika KD, Drabowicz J, Sato A, Aceña JL, Soloshonok VA. The self-disproportionation of the enantiomers (SDE) of methyl n-pentyl sulfoxide via achiral, gravity-driven column chromatography: a case study. Organic & Biomolecular Chemistry. 12: 4738-46. PMID 24873904 DOI: 10.1039/C4Ob00831F |
0.351 |
|
| 2014 |
Wu L, Xie C, Mei H, Soloshonok VA, Han J, Pan Y. Highly efficient and generalized asymmetric synthesis of quaternary stereogenic carbon-containing β-amino indanones/indanoles via Mannich-type additions between 1-indanones and N-tert-butanesulfinylketimines. Organic & Biomolecular Chemistry. 12: 4620-7. PMID 24850244 DOI: 10.1039/c4ob00489b |
0.369 |
|
| 2014 |
Moriwaki H, Resch D, Li H, Ojima I, Takeda R, Aceña JL, Soloshonok VA. Synthesis and stereochemical assignments of diastereomeric Ni(II) complexes of glycine Schiff base with (R)-2-(N-{2-[N-alkyl-N-(1-phenylethyl)amino]acetyl}amino)benzophenone; a case of configurationally stable stereogenic nitrogen. Beilstein Journal of Organic Chemistry. 10: 442-8. PMID 24605164 DOI: 10.3762/Bjoc.10.41 |
0.438 |
|
| 2014 |
Mei H, Xiong Y, Xie C, Soloshonok VA, Han J, Pan Y. Concise and scalable asymmetric synthesis of 5-(1-amino-2,2,2-trifluoroethyl)thiazolo[3,2-b][1,2,4]triazoles. Organic & Biomolecular Chemistry. 12: 2108-13. PMID 24553668 DOI: 10.1039/c3ob42348d |
0.302 |
|
| 2014 |
Han J, Ono T, Uekusa H, Klika KD, Soloshonok VA. Substituent-controlled preference of carbonyl group-metal coordination in d8 metal complexes with non-symmetric pentadentate ligands. Structural and stereochemical aspects. Dalton Transactions (Cambridge, England : 2003). 43: 5375-81. PMID 24519315 DOI: 10.1039/C3Dt53312C |
0.354 |
|
| 2014 |
Shibata N, Nishimine T, Shibata N, Tokunaga E, Kawada K, Kagawa T, Aceña JL, Sorochinsky AE, Soloshonok VA. Asymmetric Mannich reaction between (S)-N-(tert-butanesulfinyl)-3,3,3-trifluoroacetaldimine and malonic acid derivatives. Stereodivergent synthesis of (R)- and (S)-3-amino-4,4,4-trifluorobutanoic acids. Organic & Biomolecular Chemistry. 12: 1454-62. PMID 24445698 DOI: 10.1039/c3ob42425a |
0.417 |
|
| 2014 |
Bergagnini M, Fukushi K, Han J, Shibata N, Roussel C, Ellis TK, Aceña JL, Soloshonok VA. NH-type of chiral Ni(II) complexes of glycine Schiff base: design, structural evaluation, reactivity and synthetic applications. Organic & Biomolecular Chemistry. 12: 1278-91. PMID 24424805 DOI: 10.1039/C3Ob41959B |
0.764 |
|
| 2014 |
Moriwaki H, Resch D, Li H, Ojima I, Takeda R, Aceña JL, Soloshonok V. Inexpensive chemical method for preparation of enantiomerically pure phenylalanine. Amino Acids. 46: 945-52. PMID 24385244 DOI: 10.1007/S00726-013-1656-0 |
0.509 |
|
| 2014 |
Maestro MA, Avecilla F, Sorochinsky AE, Ellis TK, Aceña JL, Soloshonok VA. Chiral N(H)-tBu and N(H)-Ad NiII complexes of glycine schiff bases: Deduction of a mode of kinetic diastereoselectivity European Journal of Organic Chemistry. 2014: 4309-4314. DOI: 10.1002/Ejoc.201402145 |
0.681 |
|
| 2014 |
Milcent T, Hao J, Kawada K, Soloshonok VA, Ongeri S, Crousse B. Highly Stereoselective aza‐Baylis–Hillman Reactions of CF3‐Sulfinylimines: Straightforward Access to α‐Methylene β‐CF3 β‐Amino Acids European Journal of Organic Chemistry. 2014: 3072-3075. DOI: 10.1002/Ejoc.201402078 |
0.465 |
|
| 2014 |
Jörres M, Chen X, Aceña JL, Merkens C, Bolm C, Liu H, Soloshonok VA. Asymmetric Synthesis of α-Amino Acids under Operationally Convenient Conditions Advanced Synthesis & Catalysis. 356: 2203-2208. DOI: 10.1002/Adsc.201400405 |
0.557 |
|
| 2013 |
Sorochinsky AE, Aceña JL, Moriwaki H, Sato T, Soloshonok V. Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 2: aldol, Mannich addition reactions, deracemization and (S) to (R) interconversion of α-amino acids. Amino Acids. 45: 1017-33. PMID 24043459 DOI: 10.1007/S00726-013-1580-3 |
0.573 |
|
| 2013 |
Sorochinsky AE, Aceña JL, Moriwaki H, Sato T, Soloshonok VA. Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases; Part 1: alkyl halide alkylations. Amino Acids. 45: 691-718. PMID 23832533 DOI: 10.1007/s00726-013-1539-4 |
0.449 |
|
| 2013 |
Sorochinsky AE, Katagiri T, Ono T, Wzorek A, Aceña JL, Soloshonok VA. Optical purifications via self-disproportionation of enantiomers by achiral chromatography: case study of a series of α-CF3-containing secondary alcohols. Chirality. 25: 365-8. PMID 23716267 DOI: 10.1002/Chir.22180 |
0.314 |
|
| 2013 |
Wang J, Liu H, Aceña JL, Houck D, Takeda R, Moriwaki H, Sato T, Soloshonok VA. Synthesis of bis-α,α'-amino acids through diastereoselective bis-alkylations of chiral Ni(II)-complexes of glycine. Organic & Biomolecular Chemistry. 11: 4508-15. PMID 23715131 DOI: 10.1039/C3Ob40594J |
0.568 |
|
| 2013 |
Sorochinsky AE, Ueki H, Aceña JL, Ellis TK, Moriwaki H, Sato T, Soloshonok VA. Chemical approach for interconversion of (S)- and (R)-α-amino acids. Organic & Biomolecular Chemistry. 11: 4503-7. PMID 23715058 DOI: 10.1039/C3Ob40541A |
0.779 |
|
| 2013 |
Ding X, Wang H, Wang J, Wang S, Lin D, Lv L, Zhou Y, Luo X, Jiang H, Aceña JL, Soloshonok VA, Liu H. Synthesis of polysubstituted β-amino cyclohexane carboxylic acids via Diels-Alder reaction using Ni(II)-complex stabilized β-alanine derived dienes. Amino Acids. 44: 791-6. PMID 23053018 DOI: 10.1007/S00726-012-1404-X |
0.512 |
|
| 2013 |
Shevchuk MV, Kukhar VP, Röschenthaler G, Bassil BS, Kawada K, Soloshonok VA, Sorochinsky AE. New asymmetric approach to β-trifluoromethyl isoserines Rsc Advances. 3: 6479. DOI: 10.1039/C3Ra40687C |
0.435 |
|
| 2013 |
Turcheniuk KV, Kukhar VP, Röschenthaler G, Aceña JL, Soloshonok VA, Sorochinsky AE. Recent advances in the synthesis of fluorinated aminophosphonates and aminophosphonic acids Rsc Advances. 3: 6693. DOI: 10.1039/C3RA22891F |
0.363 |
|
| 2013 |
Aceña JL, Sorochinsky AE, Moriwaki H, Sato T, Soloshonok VA. Synthesis of fluorine-containing α-amino acids in enantiomerically pure form via homologation of Ni(II) complexes of glycine and alanine Schiff bases Journal of Fluorine Chemistry. 155: 21-38. DOI: 10.1016/J.JFLUCHEM.2013.06.004 |
0.434 |
|
| 2013 |
Sorochinsky AE, Ueki H, Aceña JL, Ellis TK, Moriwaki H, Sato T, Soloshonok VA. Chemical deracemization and (S) to (R) interconversion of some fluorine-containing α-amino acids Journal of Fluorine Chemistry. 152: 114-118. DOI: 10.1016/J.Jfluchem.2013.02.022 |
0.778 |
|
| 2013 |
Xie C, Mei H, Wu L, Soloshonok VA, Han J, Pan Y. Concise Asymmetric Synthesis of β-Trifluoromethylated α,β-Diamino Esters through Addition Reactions of Glycine Esters to CF3-Sulfinylimine European Journal of Organic Chemistry. 2014: 1445-1451. DOI: 10.1002/EJOC.201301377 |
0.319 |
|
| 2012 |
Soloshonok VA, Aceña JL, Ueki H, Han J. Design and synthesis of quasi-diastereomeric molecules with unchanging central, regenerating axial and switchable helical chirality via cleavage and formation of Ni(II)-O and Ni(II)-N coordination bonds. Beilstein Journal of Organic Chemistry. 8: 1920-8. PMID 23209532 DOI: 10.3762/Bjoc.8.223 |
0.357 |
|
| 2012 |
Turcheniuk KV, Poliashko KO, Kukhar VP, Rozhenko AB, Soloshonok VA, Sorochinsky AE. Efficient asymmetric synthesis of trifluoromethylated β-aminophosphonates and their incorporation into dipeptides. Chemical Communications (Cambridge, England). 48: 11519-21. PMID 23090101 DOI: 10.1039/c2cc36702e |
0.366 |
|
| 2012 |
Röschenthaler G, Kukhar VP, Kulik IB, Belik MY, Sorochinsky AE, Rusanov EB, Soloshonok VA. Asymmetric synthesis of phosphonotrifluoroalanine and its derivatives using N-tert-butanesulfinyl imine derived from fluoral Tetrahedron Letters. 53: 539-542. DOI: 10.1016/J.Tetlet.2011.11.096 |
0.441 |
|
| 2012 |
Nakamura T, Tateishi K, Tsukagoshi S, Hashimoto S, Watanabe S, Soloshonok VA, Aceña JL, Kitagawa O. Self-disproportionation of enantiomers of non-racemic chiral amine derivatives through achiral chromatography Tetrahedron. 68: 4013-4017. DOI: 10.1016/J.Tet.2012.03.054 |
0.384 |
|
| 2012 |
Houck D, Luisaceña J, Soloshonok VA. Alkylations of chiral nickel(II) complexes of glycine under phase-transfer conditions Helvetica Chimica Acta. 95: 2672-2679. DOI: 10.1002/Hlca.201200536 |
0.43 |
|
| 2012 |
Acena JL, Sorochinsky AE, Soloshonok VA. ChemInform Abstract: Recent Advances in the Asymmetric Synthesis of α-(Trifluoromethyl)-Containing α-Amino Acids Cheminform. 43: no-no. DOI: 10.1002/CHIN.201231244 |
0.393 |
|
| 2011 |
Soloshonok VA, Nelson DJ. Alkene selenenylation: A comprehensive analysis of relative reactivities, stereochemistry and asymmetric induction, and their comparisons with sulfenylation. Beilstein Journal of Organic Chemistry. 7: 744-58. PMID 21804870 DOI: 10.3762/Bjoc.7.85 |
0.377 |
|
| 2011 |
Wang J, Lin D, Zhou S, Ding X, Soloshonok VA, Liu H. Asymmetric synthesis of sterically and electronically demanding linear ω-trifluoromethyl containing amino acids via alkylation of chiral equivalents of nucleophilic glycine and alanine. The Journal of Organic Chemistry. 76: 684-7. PMID 21182272 DOI: 10.1021/jo102031b |
0.441 |
|
| 2011 |
Mikami K, Fustero S, Sánchez-Roselló M, Aceña JL, Soloshonok V, Sorochinsky A. Synthesis of Fluorinated β-AminoAcids Synthesis. 2011: 3045-3079. DOI: 10.1055/S-0030-1260173 |
0.372 |
|
| 2011 |
Röschenthaler G, Kukhar VP, Kulik IB, Sorochinsky AE, Soloshonok VA. Convenient synthesis of fluoroalkyl α- and β-aminophosphonates Journal of Fluorine Chemistry. 132: 834-837. DOI: 10.1016/J.Jfluchem.2011.05.005 |
0.452 |
|
| 2010 |
Soloshonok V, Sorochinsky A. Practical Methods for the Synthesis of Symmetrically α,α-Disubstituted α-Amino Acids Synthesis. 2010: 2319-2344. DOI: 10.1055/S-0029-1220013 |
0.521 |
|
| 2010 |
Yagupolskii YL, Soloshonok VA. Fluorine chemistry in Ukraine Journal of Fluorine Chemistry. 131: 123-126. DOI: 10.1016/J.Jfluchem.2009.12.011 |
0.325 |
|
| 2010 |
Yasumoto M, Ueki H, Soloshonok VA. Self-disproportionation of enantiomers of α-trifluoromethyl lactic acid amides via sublimation Journal of Fluorine Chemistry. 131: 540-544. DOI: 10.1016/j.jfluchem.2009.11.010 |
0.316 |
|
| 2010 |
Sorochinsky AE, Soloshonok VA. Asymmetric synthesis of fluorine-containing amines, amino alcohols, α- and β-amino acids mediated by chiral sulfinyl group Journal of Fluorine Chemistry. 131: 127-139. DOI: 10.1016/j.jfluchem.2009.09.015 |
0.4 |
|
| 2010 |
Soloshonok VA, Sorochinsky AE. ChemInform Abstract: Practical Methods for the Synthesis of Symmetrically α,α-Disubstituted α-Amino Acids Cheminform. 41: no-no. DOI: 10.1002/CHIN.201044240 |
0.35 |
|
| 2010 |
Soloshonok VA, Ueki H, Ellis TK. ChemInform Abstract: Michael Addition Reactions Between Nucleophilic Glycine Equivalents and Acrylic Acid Derivatives as a Practical and Generalized Approach to the Asymmetric Synthesis of β-Substituted α-Amino Acids Cheminform. 41: no-no. DOI: 10.1002/chin.201001243 |
0.764 |
|
| 2010 |
ARNONE A, BRAVO P, FRIGERIO M, MEILLE SV, ROMITA V, VIANI F, ZAPPALA C, SOLOSHONOK VA, SHISHKIN OV, STRUCHKOV YT. ChemInform Abstract: Reactions of α-Substituted β-Keto-γ-fluoro Sulfoxides with Diazomethane. A General Approach to Enantiomerically Pure α-Fluoromethyl-α′,α′-alkyl/alkenyl-sulfinylmethyl Oxiranes. Cheminform. 29: no-no. DOI: 10.1002/chin.199842109 |
0.323 |
|
| 2010 |
SOLOSHONOK VA. ChemInform Abstract: Practical Synthesis of Enantiopure Fluoroamino Acids of Biological Interest by Asymmetric Aldol Reactions Cheminform. 28: no-no. DOI: 10.1002/chin.199710215 |
0.397 |
|
| 2010 |
KUKHAR VP, RESNATI G, SOLOSHONOK VA. ChemInform Abstract: Asymmetric Synthesis of Fluorine-Containing Amino Acids Cheminform. 27: no-no. DOI: 10.1002/chin.199603298 |
0.414 |
|
| 2010 |
SOLOSHONOK VA, FOKINA NA, RYBAKOVA AV, SHISHKINA IP, GALUSHKO SV, SOROCHINSKY AE, KUKHAR VP, SAVCHENKO MV, SVEDAS VK. ChemInform Abstract: Biocatalytic Approach to Enantiomerically Pure β-Amino Acids. Cheminform. 27: no-no. DOI: 10.1002/chin.199601106 |
0.358 |
|
| 2010 |
SOLOSHONOK VA, SVISTUNOVA NY, KUKHAR' VP, KUZ'MINA NA, POPOV VI, BELOKON' YN. ChemInform Abstract: Asymmetric Synthesis of Organo-Element Analogs of Natural Products. Part 17. Fluorine-Containing (S)-Homocysteic Acid Esters. Cheminform. 25: no-no. DOI: 10.1002/chin.199420245 |
0.344 |
|
| 2010 |
SOLOSHONOK VA, KUKHAR VP, GALUSHKO SV, SVISTUNOVA NY, AVILOV DV, KUZ'MINA NA, RAEVSKI NI, STRUCHKOV YT, PYSAREVSKY AP, BELOKON YN. ChemInform Abstract: General Method for the Synthesis of Enantiomerically Pure β- Hydroxy-α-amino Acids, Containing Fluorine Atoms in the Side Chains. Case of Stereochemical Distinction Between Methyl and Trifluoromethyl Groups. X-Ray Crystal and Molecula Cheminform. 25: no-no. DOI: 10.1002/chin.199412268 |
0.323 |
|
| 2010 |
SOLOSHONOK VA, SVISTUNOVA NY, KUKHAR' VP, SOLODENKO VA, KUZ'MINA NA, ROZHENKO AB, GALUSHKO SV, SHISHKINA IP, GUDIMA AO, BELOKON' YN. ChemInform Abstract: Asymmetric Synthesis of Organoelement Analogs of Natural Compounds. Part 6. (S)-α-Amino-ω-phosphonocarboxylic Acids. Cheminform. 24: no-no. DOI: 10.1002/chin.199336217 |
0.419 |
|
| 2010 |
SOLOSHONOK VA, KUKHAR' VP, GALUSHKO SV, KOLYCHEVA MT, ROZHENKO AB, BELOKON' YN. ChemInform Abstract: Asymmetric Synthesis of Elementoorganic Analogs of Natural Compounds. Part 3. A General Method for Diastereo- and Enantioselective Synthesis of Fluorine-Containing 2(R),3(S)-β-Phenylserines. Cheminform. 23: no-no. DOI: 10.1002/chin.199250273 |
0.332 |
|
| 2009 |
Kukhar VP, Sorochinsky AE, Soloshonok VA. Practical synthesis of fluorine-containing α- and β-amino acids: recipes from Kiev, Ukraine. Future Medicinal Chemistry. 1: 793-819. PMID 21426081 DOI: 10.4155/fmc.09.70 |
0.455 |
|
| 2009 |
Soloshonok VA, Ellis TK, Ueki H, Ono T. Resolution/deracemization of chiral alpha-amino acids using resolving reagents with flexible stereogenic centers. Journal of the American Chemical Society. 131: 7208-9. PMID 19422236 DOI: 10.1021/Ja9026055 |
0.729 |
|
| 2009 |
Ueki H, Soloshonok VA. New sterically driven mode for generation of helical chirality. Organic Letters. 11: 1797-800. PMID 19354321 DOI: 10.1021/Ol900357D |
0.309 |
|
| 2009 |
Soloshonok V, Ueki H. Towards Modular Design of Chiroptically Switchable Molecules Based on Formation and Cleavage of Metal-Ligand Coordination Bonds Synthesis. 2010: 49-56. DOI: 10.1055/S-0029-1217090 |
0.388 |
|
| 2009 |
Soloshonok VA, Ueki H, Ellis TK. New generation of modular nucleophilic glycine equivalents for the general synthesis of α-amino acids Synlett. 0704-0715. DOI: 10.1055/S-0028-1087929 |
0.796 |
|
| 2009 |
Ellis TK, Ueki H, Tiwari R, Soloshonok VA. Michael addition reactions between various nucleophilic glycine equivalents and (S,E)-1-enoyl-5-oxo-N-phenylpyrrolidine-2-carboxamide, an optimal type of chiral Michael acceptor in the asymmetric synthesis of β-phenyl pyroglutamic acid and related compounds Tetrahedron Asymmetry. 20: 2629-2634. DOI: 10.1016/J.Tetasy.2009.10.006 |
0.763 |
|
| 2009 |
Soloshonok VA, Ono T. Operationally convenient asymmetric synthesis of (S)-2-amino-3,3-bis-(4-fluorophenyl)propanoic acid Journal of Fluorine Chemistry. 130: 547-549. DOI: 10.1016/j.jfluchem.2009.03.005 |
0.416 |
|
| 2009 |
Soloshonok VA, Ueki H, Ellis TK. ChemInform Abstract: Modular Approach to the Design of Nucleophilic Glycine Equivalents with Tailorable Physicochemical Properties Cheminform. 40: no-no. DOI: 10.1002/chin.200951242 |
0.653 |
|
| 2009 |
Soloshonok VA, Ueki H, Ellis TK. ChemInform Abstract: New Generation of Modular Nucleophilic Glycine Equivalents for the General Synthesis of α-Amino Acids Cheminform. 40. DOI: 10.1002/chin.200927249 |
0.758 |
|
| 2008 |
Soloshonok V, Boettiger T, Bolene S. Asymmetric Synthesis of (2S,3S)- and (2R,3R)-α,β-Dialkyl-α-amino Acids via Alkylation of Chiral Nickel(II) Complexes of Aliphatic α-Amino Acids with Racemic α-Alkylbenzyl Bromides Synthesis. 2008: 2594-2602. DOI: 10.1055/S-2008-1067172 |
0.534 |
|
| 2008 |
Soloshonok V, Ueki H. Efficient and Practical Protection of the Catechol Residue of 3,4-Dihydroxyphenylalanine (DOPA) Derivative as Acetonide Synthesis. 2008: 693-695. DOI: 10.1055/S-2008-1032164 |
0.399 |
|
| 2008 |
Yamada T, Sakaguchi K, Shinada T, Ohfune Y, Soloshonok VA. Efficient asymmetric synthesis of the functionalized pyroglutamate core unit common to oxazolomycin and neooxazolomycin using Michael reaction of nucleophilic glycine Schiff base with α,β-disubstituted acrylate Tetrahedron: Asymmetry. 19: 2789-2795. DOI: 10.1016/j.tetasy.2008.11.036 |
0.34 |
|
| 2007 |
Soloshonok VA, Ueki H, Moore JL, Ellis TK. Design and synthesis of molecules with switchable chirality via formation and cleavage of metal-ligand coordination bonds. Journal of the American Chemical Society. 129: 3512-3. PMID 17338523 DOI: 10.1021/Ja067995R |
0.679 |
|
| 2007 |
Soloshonok VA, Yasumoto M. Catalytic asymmetric synthesis of α-(trifluoromethyl)benzylamine via cinchonidine derived base-catalyzed biomimetic 1,3-proton shift reaction Journal of Fluorine Chemistry. 128: 170-173. DOI: 10.1016/j.jfluchem.2006.11.011 |
0.354 |
|
| 2006 |
Yamada T, Okada T, Sakaguchi K, Ohfune Y, Ueki H, Soloshonok VA. Efficient asymmetric synthesis of novel 4-substituted and configurationally stable analogues of thalidomide. Organic Letters. 8: 5625-8. PMID 17107088 DOI: 10.1021/Ol0623668 |
0.391 |
|
| 2006 |
Ellis TK, Ueki H, Yamada T, Ohfune Y, Soloshonok VA. Design, synthesis, and evaluation of a new generation of modular nucleophilic glycine equivalents for the efficient synthesis of sterically constrained alpha-amino acids. The Journal of Organic Chemistry. 71: 8572-8. PMID 17064036 DOI: 10.1021/Jo0616198 |
0.759 |
|
| 2006 |
Ellis TK, Soloshonok VA. Design and synthesis of a new generation of 'NH'-Ni(II) complexes of glycine Schiff bases and their unprecedented C-H vs. N-H chemoselectivity in alkyl halide alkylations and Michael addition reactions Synlett. 533-538. DOI: 10.1055/S-2006-926252 |
0.765 |
|
| 2006 |
Soloshonok VA, Yamada T, Ueki H, Moore AM, Cook TK, Arbogast KL, Soloshonok AV, Martin CH, Ohfune Y. Operationally convenient, efficient asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via methylene dimerization of chiral glycine equivalents with dichloromethane Tetrahedron. 62: 6412-6419. DOI: 10.1016/j.tet.2006.04.023 |
0.395 |
|
| 2006 |
Soloshonok VA, Ohkura H, Yasumoto M. Operationally convenient asymmetric synthesis of (S)- and (R)-3-amino-4,4,4-trifluorobutanoic acid Journal of Fluorine Chemistry. 127: 930-935. DOI: 10.1016/j.jfluchem.2006.04.004 |
0.36 |
|
| 2006 |
Soloshonok VA, Ohkura H, Yasumoto M. Operationally convenient asymmetric synthesis of (S)- and (R)-3-amino-4,4,4-trifluorobutanoic acid Journal of Fluorine Chemistry. 127: 924-929. DOI: 10.1016/j.jfluchem.2006.04.003 |
0.36 |
|
| 2006 |
Soloshonok VA, Ohkura H, Yasumoto M. Operationally Convenient Asymmetric Synthesis of (S)- and (R)-3-Amino-4,4,4-trifluorobutanoic Acid. Part 2. Enantioselective Biomimetic Transamination of 4,4,4-Trifluoro-3-oxo-N-[(R)-1-phenylethyl]butanamide. Cheminform. 37. DOI: 10.1002/chin.200644188 |
0.314 |
|
| 2006 |
Soloshonok VA, Ohkura H, Yasumoto M. Operationally Convenient Asymmetric Synthesis of (S)- and (R)-3-Amino-4,4,4-trifluorobutanoic Acid. Part 1. Enantioselective Biomimetic Transamination of Isopropyl 4,4,4-Trifluoro-3-oxo-butanoate. Cheminform. 37. DOI: 10.1002/chin.200644187 |
0.382 |
|
| 2005 |
Soloshonok VA, Cai C, Yamada T, Ueki H, Ohfune Y, Hruby VJ. Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity. Journal of the American Chemical Society. 127: 15296-303. PMID 16248672 DOI: 10.1021/Ja0535561 |
0.404 |
|
| 2005 |
Soloshonok VA, Ueki H, Ellis TK, Yamada T, Ohfune Y. Application of modular nucleophilic glycine equivalents for truly practical asymmetric synthesis of β-substituted pyroglutamic acids Tetrahedron Letters. 46: 1107-1110. DOI: 10.1016/J.Tetlet.2004.12.093 |
0.773 |
|
| 2005 |
Ellis TK, Ueki H, Soloshonok VA. New generation of nucleophilic glycine equivalents Tetrahedron Letters. 46: 941-944. DOI: 10.1016/J.Tetlet.2004.12.050 |
0.694 |
|
| 2005 |
Soloshonok VA, Ueki H, Ellis TK, Yamada T, Ohfune Y. Application of Modular Nucleophilic Glycine Equivalents for Truly Practical Asymmetric Synthesis of β-Substituted Pyroglutamic Acids. Cheminform. 36. DOI: 10.1002/chin.200523200 |
0.747 |
|
| 2005 |
Berbasov DO, Ellis TK, Soloshonok VA. Biocatalytic Entry to Enantiomerically Pure β-Amino Acids Enantioselective Synthesis of β-Amino Acids: Second Edition. 397-414. DOI: 10.1002/0471698482.ch17 |
0.725 |
|
| 2004 |
Soloshonok VA, Ueki H, Tiwari R, Cai C, Hruby VJ. Virtually complete control of simple and face diastereoselectivity in the Michael addition reactions between achiral equivalents of a nucleophilic glycine and (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: practical method for preparation of beta-substituted pyroglutamic acids and prolines. The Journal of Organic Chemistry. 69: 4984-90. PMID 15255725 DOI: 10.1021/Jo0495438 |
0.447 |
|
| 2004 |
Uytterhoeven K, Soloshonok V, Meervelt Lv. Crystal structure of {(5)-N-[2-(N-benzylprolyl)aminobenzophenone]-[(2S,3R)-3-N-[(4-methoxycarbonyl)phenylamine]-3-phenylpropanoic acid-O,N,N',N"]}nickel(II), Ni(C42H38N4O5) Zeitschrift Fur Kristallographie-New Crystal Structures. 219: 453-454. DOI: 10.1524/Ncrs.2004.219.14.485 |
0.31 |
|
| 2004 |
Taylor SM, Yamada T, Ueki H, Soloshonok VA. Asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via methylenedimerization of chiral glycine equivalents with dichloromethane under operationally convenient conditions Tetrahedron Letters. 45: 9159-9162. DOI: 10.1016/j.tetlet.2004.10.111 |
0.405 |
|
| 2004 |
Cai C, Yamada T, Tiwari R, Hruby VJ, Soloshonok VA. Application of (S)- and (R)-methyl pyroglutamates as inexpensive, yet highly efficient chiral auxiliaries in the asymmetric Michael addition reactions Tetrahedron Letters. 45: 6855-6858. DOI: 10.1016/J.Tetlet.2004.07.096 |
0.45 |
|
| 2003 |
Sorochinsky A, Voloshin N, Markovsky A, Belik M, Yasuda N, Uekusa H, Ono T, Berbasov DO, Soloshonok VA. Convenient asymmetric synthesis of beta-substituted alpha,alpha-difluoro-beta-amino acids via Reformatsky reaction between Davis' N-sulfinylimines and ethyl bromodifluoroacetate. The Journal of Organic Chemistry. 68: 7448-54. PMID 12968899 DOI: 10.1021/jo030082k |
0.319 |
|
| 2003 |
Ueki H, Ellis TK, Martin CH, Boettiger TU, Bolene SB, Soloshonok VA. Improved synthesis of proline-derived Ni(II) complexes of glycine: versatile chiral equivalents of nucleophilic glycine for general asymmetric synthesis of alpha-amino acids. The Journal of Organic Chemistry. 68: 7104-7. PMID 12946159 DOI: 10.1021/Jo0301494 |
0.754 |
|
| 2003 |
Ellis TK, Martin CH, Tsai GM, Ueki H, Soloshonok VA. Efficient synthesis of serically constrained smmetrically alpha,alpha-disubstituted alpha-amino acids under operationally convenient conditions. The Journal of Organic Chemistry. 68: 6208-14. PMID 12895052 DOI: 10.1021/Jo030075W |
0.671 |
|
| 2003 |
Ellis TK, Hochla VM, Soloshonok VA. Efficient synthesis of 2-aminoindane-2-carboxylic acid via dialkylation of nucleophilic glycine equivalent. The Journal of Organic Chemistry. 68: 4973-6. PMID 12790614 DOI: 10.1021/Jo030065V |
0.775 |
|
| 2003 |
Berbasov DO, Soloshonok VA. Chemoselectivity in the Reactions Between Ethyl 4,4,4-Trifluoro-3-oxobutanoate and Anilines: Improved Synthesis of 2-Trifluoromethyl-4- and 4-Trifluoromethyl-2-quinolinones Synthesis. 2003: 2005-2010. DOI: 10.1055/S-2003-41043 |
0.411 |
|
| 2003 |
Ohkura H, Berbasov DO, Soloshonok VA. Simple and highly diastereoselective synthesis of trifluoromethyl-containing myosmines via reaction between 2-(aminomethyl)pyridine and 1,1,1,5,5,5-hexafluoro-2,4-pentanedione Tetrahedron Letters. 44: 2417-2420. DOI: 10.1016/S0040-4039(03)00244-2 |
0.318 |
|
| 2003 |
Ellis TK, Martin CH, Ueki H, Soloshonok VA. Efficient, practical synthesis of symmetrically α,α-disubstituted α-amino acids Tetrahedron Letters. 44: 1063-1066. DOI: 10.1016/S0040-4039(02)02719-3 |
0.747 |
|
| 2003 |
Ueki H, Ellis TK, Khan MA, Soloshonok VA. Highly diastereoselective synthesis of new, carbostyril-based type of conformationally-constrained β-phenylserines Tetrahedron. 59: 7301-7306. DOI: 10.1016/S0040-4020(03)01172-4 |
0.725 |
|
| 2003 |
Ueki H, Ellis T, Martin C, Soloshonok V. Efficient Large-Scale Synthesis of Picolinic Acid-Derived Nickel(II) Complexes of Glycine European Journal of Organic Chemistry. 2003: 1954-1957. DOI: 10.1002/ejoc.200200688 |
0.72 |
|
| 2003 |
Ellis TK, Martin CH, Tsai GM, Ueki H, Soloshonok VA. Efficient Synthesis of Sterically Constrained Symmetrically α,α-Disubstituted α-Amino Acids under Operationally Convenient Conditions. Cheminform. 34. DOI: 10.1002/chin.200349071 |
0.728 |
|
| 2002 |
Soloshonok VA, Ohkura H, Uneyama K. Biomimetic reductive amination of perfluoroalkylcarboxylic acids to α,α-dihydroperfluoroalkylamines Tetrahedron Letters. 43: 5449-5452. DOI: 10.1016/S0040-4039(02)01104-8 |
0.321 |
|
| 2002 |
Soloshonok VA, Ohkura H, Sorochinsky A, Voloshin N, Markovsky A, Belik M, Yamazaki T. Convenient, large-scale asymmetric synthesis of β-aryl-substituted α,α-difluoro-β-amino acids Tetrahedron Letters. 43: 5445-5448. DOI: 10.1016/S0040-4039(02)01103-6 |
0.355 |
|
| 2001 |
Cai C, Soloshonok VA, Hruby VJ. Michael addition reactions between chiral Ni(II) complex of glycine and 3-(trans-enoyl)oxazolidin-2-ones. A case of electron donor-acceptor attractive interaction-controlled face diastereoselectivity. The Journal of Organic Chemistry. 66: 1339-50. PMID 11312965 DOI: 10.1021/Jo0014865 |
0.37 |
|
| 2001 |
Soloshonok VA, Tang X, Hruby VJ. Large-scale asymmetric synthesis of novel sterically constrained 2′,6′-dimethyl- and α,2′,6′-trimethyltyrosine and -phenylalanine derivatives via alkylation of chiral equivalents of nucleophilic glycine and alanine Tetrahedron. 57: 6375-6382. DOI: 10.1016/S0040-4020(01)00504-X |
0.413 |
|
| 2001 |
Hruby VJ, Soloshonok VA. Asymmetric synthesis of novel sterically constrained amino acids Tetrahedron. 57. DOI: 10.1016/S0040-4020(01)00498-7 |
0.412 |
|
| 2001 |
Soloshonok VA, Tang X, Hruby VJ, Van Meervelt L. ChemInform Abstract: Asymmetric Synthesis of α,β-Dialkyl-α-phenylalanines via Direct Alkylation of a Chiral Alanine Derivative with Racemic α-Alkylbenzyl Bromides. A Case of High Enantiomer Differentiation at Room Temperature. Cheminform. 32: no-no. DOI: 10.1002/chin.200120166 |
0.311 |
|
| 2001 |
Soloshonok VA, Cai C, Hruby VJ, Meervelt LV, Yamazaki T. ChemInform Abstract: Stereochemically Defined C-Substituted Glutamic Acids and Their Derivatives. Part 7. Rational Design of Highly Diastereoselective, Organic Base-Catalyzed, Room-Temperature Michael Addition Reactions. Cheminform. 32: no-no. DOI: 10.1002/chin.200106055 |
0.332 |
|
| 2000 |
Soloshonok VA, Cai C, Hruby VJ, Van Meervelt L, Yamazaki T. Rational design of highly diastereoselective, organic base-catalyzed, room-temperature Michael addition reactions. The Journal of Organic Chemistry. 65: 6688-96. PMID 11052120 DOI: 10.1021/Jo0008791 |
0.385 |
|
| 2000 |
Tang X, Soloshonok VA, Hruby VJ. Convenient, asymmetric synthesis of enantiomerically pure 2′,6′-dimethyltyrosine (DMT) via alkylation of chiral equivalent of nucleophilic glycine Tetrahedron: Asymmetry. 11: 2917-2925. DOI: 10.1016/S0957-4166(00)00250-0 |
0.45 |
|
| 2000 |
Soloshonok VA, Cai C, Hruby VJ. Toward design of a practical methodology for stereocontrolled synthesis of χ-constrained pyroglutamic acids and related compounds. Virtually complete control of simple diastereoselectivity in the Michael addition reactions of glycine Ni(II) complexes with N-(enoyl)oxazolidinones Tetrahedron Letters. 41: 135-139. DOI: 10.1016/S0040-4039(99)02018-3 |
0.464 |
|
| 2000 |
Qiu W, Soloshonok VA, Cai C, Tang X, Hruby VJ. Convenient, Large-Scale Asymmetric Synthesis of Enantiomerically Pure trans-Cinnamylglycine and -α-Alanine Tetrahedron. 56: 2577-2582. DOI: 10.1016/S0040-4020(00)00176-9 |
0.45 |
|
| 1999 |
Soloshonok VA, Cai C, Hruby VJ. Asymmetric Michael addition reactions of chiral Ni(II)-complex of glycine with (N-trans-enoyl)oxazolidines: Improved reactivity and stereochemical outcome Tetrahedron Asymmetry. 10: 4265-4269. DOI: 10.1016/S0957-4166(99)00483-8 |
0.398 |
|
| 1999 |
Soloshonok VA, Cai C, Hruby VJ, Van Meervelt L, Mischenko N. Stereochemically defined C-substituted glutamic acids and their derivatives. 1. An efficient asymmetric synthesis of (2S,3S)-3-methyl- and -3-trifluoromethylpyroglutamic acids Tetrahedron. 55: 12031-12044. DOI: 10.1016/S0040-4020(99)00711-5 |
0.439 |
|
| 1999 |
Soloshonok VA, Cai C, Hruby VJ, Van Meervelt L. Asymmetric synthesis of novel highly sterically constrained (2S,3S)-3-methyl-3-trifluoromethyl- and (2S,3S,4R)-3-trifluoromethyl-4-methylpyroglutamic acids Tetrahedron. 55: 12045-12058. DOI: 10.1016/S0040-4020(99)00710-3 |
0.369 |
|
| 1999 |
Bravo P, Capelli S, Crucianelli M, Guidetti M, Markovsky AL, Meille SV, Soloshonok VA, Sorochinsky AE, Viani F, Zanda M. Asymmetric synthesis of α-arylglycinols via additions of lithium methyl p-tolyl sulfoxide to N-(PMP)arylaldimines followed by “non oxidative” Pummerer reaction Tetrahedron. 55: 3025-3040. DOI: 10.1016/S0040-4020(99)00064-2 |
0.309 |
|
| 1998 |
Soloshonok VA, Soloshonok IV, Kukhar VP, Svedas VK. Biomimetic Transamination of α-Alkyl β-Keto Carboxylic Esters. Chemoenzymatic Approach to the Stereochemically Defined α-Alkyl β-Fluoroalkyl β-Amino Acids The Journal of Organic Chemistry. 63: 1878-1884. DOI: 10.1021/Jo971777M |
0.427 |
|
| 1998 |
Arnone A, Bravo P, Frigerio M, Viani F, Soloshonok VA. Highly diastereoselective methylene transfer from diazomethane to the carbonyl of β-keto sulfoxides. A general approach to synthetically versatile fluorine-containing chiral building blocks Tetrahedron. 54: 11841-11860. DOI: 10.1016/S0040-4020(98)83043-3 |
0.302 |
|
| 1998 |
Bravo P, Guidetti M, Viani F, Zanda M, Markovsky AL, Sorochinsky AE, Soloshonok IV, Soloshonok VA. Chiral sulfoxide controlled asymmetric additions to CN double bond. An efficient approach to stereochemically defined α-fluoroalkyl amino compounds Tetrahedron. 54: 12789-12806. DOI: 10.1016/S0040-4020(98)00779-0 |
0.328 |
|
| 1997 |
Soloshonok VA, Ono aT, Soloshonok IV. Enantioselective Biomimetic Transamination of β-Keto Carboxylic Acid Derivatives. An Efficient Asymmetric Synthesis of β-(Fluoroalkyl) β-Amino Acids Journal of Organic Chemistry. 62: 7538-7539. DOI: 10.1021/Jo9710238 |
0.466 |
|
| 1997 |
Bravo P, Farina A, Kukhar VP, Markovsky AL, Meille SV, Soloshonok VA, Sorochinsky AE, Viani F, Zanda M, Zappalà C. Stereoselective Additions Of Alpha -Lithiated Alkyl-P-Tolylsulfoxides To N-Pmp(Fluoroalkyl)Aldimines. An Efficient Approach To Enantiomerically Pure F Luoro Amino Compounds Journal of Organic Chemistry. 62: 3424-3425. DOI: 10.1021/Jo970004V |
0.372 |
|
| 1997 |
Soloshonok VA, Avilov DV, Kukhar' VP, Van Meervelt L, Mischenko N. An efficient asymmetric synthesis of (2S,3S)-3-trifluoromethylpyroglutamic acid Tetrahedron Letters. 38: 4903-4904. DOI: 10.1016/S0040-4039(97)01054-X |
0.316 |
|
| 1997 |
Sorochinsky AE, Petrenko AA, Soloshonok VA, Resnati G. Regioselective Oxyfunctionalization of Bridgehead Adamantane Derivatives Tetrahedron. 53: 5995-6000. DOI: 10.1016/S0040-4020(97)00292-5 |
0.316 |
|
| 1996 |
Ono T, Kukhar VP, Soloshonok VA. Biomimetic Reductive Amination of Fluoro Aldehydes and Ketones via [1,3]-Proton Shift Reaction.(1) Scope and Limitations. The Journal of Organic Chemistry. 61: 6563-6569. PMID 11667521 DOI: 10.1021/Jo960503G |
0.436 |
|
| 1996 |
Kukhar V, Solodenko V, Soloshonok V, Kasheva T. Synthesis of Enantiomeric Aminophosphonic Acids and Peptides Phosphorus, Sulfur, and Silicon and the Related Elements. 109: 529-532. DOI: 10.1080/10426509608545207 |
0.452 |
|
| 1996 |
Soloshonok VA, Ono T. The Effect Of Substituents On The Feasibility Of 1,3-Proton Shift Reaction: New Synthetic Opportunities Synlett. 1996: 919-921. DOI: 10.1055/S-1996-5621 |
0.345 |
|
| 1996 |
Favretto D, Traldi P, Resnati G, Soloshonok VA. Fast atom bombardment mass spectrometry in the characterization of some enantiomerically pure fluorinated β-phenylserines Journal of Fluorine Chemistry. 80: 41-45. DOI: 10.1016/S0022-1139(96)03458-6 |
0.311 |
|
| 1996 |
Soloshonok VA, Avilov DV, Kukhar' VP. Highly diastereoselective asymmetric aldol reactions of chiral Ni(II)-complex of glycine with alkyl trifluoromethyl ketones Tetrahedron: Asymmetry. 7: 1547-1550. DOI: 10.1016/0957-4166(96)00177-2 |
0.34 |
|
| 1996 |
Soloshonok VA, Kacharov AD, Avilov DV, Hayashi T. Transition metal-catalyzed diastereoselective aldol reactions of prochiral ketones with methyl isocyanoacetate Tetrahedron Letters. 37: 7845-7848. DOI: 10.1016/0040-4039(96)01746-7 |
0.345 |
|
| 1996 |
Soloshonok VA, Avilov DV, Kukhar VP. Asymmetric aldol reactions of trifluoromethyl ketones with a chiral Ni(II) complex of glycine: Stereocontrolling effect of the trifluoromethyl group Tetrahedron. 52: 12433-12442. DOI: 10.1016/0040-4020(96)00741-7 |
0.304 |
|
| 1996 |
Soloshonok VA, Kacharov AD, Hayashi T. Gold(I)-catalyzed asymmetric aldol reactions of isocyanoacetic acid derivatives with fluoroaryl aldehydes Tetrahedron. 52: 245-254. DOI: 10.1016/0040-4020(95)00893-D |
0.406 |
|
| 1995 |
Soloshonok VA, Avilov DV, Kukhar' VP, Tararov VI, Savel'eva TF, Churkina TD, Ikonnikov NS, Kochetkov KA, Orlova SA, Pysarevsky AP, Struchkov YT, Raevsky NI, Belokon' YN. Asymmetric aldol reactions of chiral Ni(II)-complex of glycine with aliphatic aldehydes. Stereodivergent synthesis of syn-(2S)- and syn-(2R)-β-alkylserines Tetrahedron: Asymmetry. 6: 1741-1756. DOI: 10.1016/0957-4166(95)00220-J |
0.536 |
|
| 1995 |
Soloshonok VA, Fokina NA, Rybakova AV, Shishkina IP, Galushko SV, Sorochinsky AE, Kukhar VP, Savchenko MV, Švedas VK. Biocatalytic approach to enantiomerically pure β-amino acids Tetrahedron: Asymmetry. 6: 1601-1610. DOI: 10.1016/0957-4166(95)00204-3 |
0.348 |
|
| 1994 |
Kukhar' VP, Soloshonok VA, Solodenko VA. Asymmetric Synthesis of Phosphorus Analogs of Amino Acids Phosphorus, Sulfur, and Silicon and the Related Elements. 92: 239-264. DOI: 10.1080/10426509408021478 |
0.402 |
|
| 1994 |
Bravo P, Capelli S, Meille SV, Viani F, Zanda M, Kukhar VP, Soloshonok VA. Synthesis of optically pure (R)- and (S)-α-trifluoromethyl-alanine Tetrahedron-Asymmetry. 5: 2009-2018. DOI: 10.1016/S0957-4166(00)86276-X |
0.332 |
|
| 1994 |
Soloshonok VA, Kirilenko AG, Galushko SV, Kukhar VP. Catalytic asymmetric synthesis of β-fluoroalkyl-β-amino acids via biomimetic [1,3]-proton shift reaction Tetrahedron Letters. 35: 5063-5064. DOI: 10.1016/S0040-4039(00)73320-X |
0.369 |
|
| 1994 |
Soloshonok VA, Kirilenko AG, Fokina NA, Kukhar VP, Galushko SV, Švedas VK, Resnati G. Chemo-enzymatic approach to the synthesis of each of the four isomers of α-alkyl-β-fluoroalkyl-substituted β-amino acids Tetrahedron: Asymmetry. 5: 1225-1228. DOI: 10.1016/0957-4166(94)80163-0 |
0.369 |
|
| 1994 |
Soloshonok VA, Hayashi T. Gold(I)-catalyzed asymmetric aldol reactions of fluorinated benzaldehydes with an α-isocyanoacetamide Tetrahedron: Asymmetry. 5: 1091-1094. DOI: 10.1016/0957-4166(94)80059-6 |
0.334 |
|
| 1994 |
Bravo P, Farina A, Frigerio M, Meille SV, Viani F, Soloshonok V. New fluorinated chiral synthons Tetrahedron: Asymmetry. 5: 987-1004. DOI: 10.1016/0957-4166(94)80049-9 |
0.401 |
|
| 1994 |
Galushko S, Shishkina I, Soloshonok V. Ligand-exchange high-performance liquid chromatography of fluorine-containing phenylglycine and phenylalanine Journal of Chromatography A. 661: 51-54. DOI: 10.1016/0021-9673(94)85176-X |
0.364 |
|
| 1993 |
Soloshonok VA, Kirilenko AG, Kukhar VP, Resnati G. A New Entry to Racemic and Optically Active -Polyfluoroalkyl--amino Acids through Biomimetic Transamination of Fluorinated -Ketocarboxylic Esters Amino Acids. 5: 130. PMID 24190649 DOI: 10.1007/Bf00806197 |
0.42 |
|
| 1993 |
Kukhar' VP, Svistunova NY, Solodenko VA, Soloshonok VA. Asymmetric synthesis of fluorine- and phosphorus-containing analogues of aminoacids Russian Chemical Reviews. 62: 261-278. DOI: 10.1070/RC1993v062n03ABEH000017 |
0.312 |
|
| 1993 |
Kukhar VP, Belokon YN, Soloshonok VA, Svistunova NY, Rozhenko AB, Kuz'mina NA. Asymmetric Synthesis of Organoelement Analogues of Natural Products; Part 12: General Method for the Asymmetric Synthesis of Fluorine-Containing Phenylalanines and α-Methyl(phenyl)alanines via Alkylation of the Chiral Nickel(II) Schiff's Base Complexes of Glycine and Alanine Synthesis. 1993: 117-120. DOI: 10.1055/S-1993-25812 |
0.505 |
|
| 1993 |
Soloshonok VA, Kukhar VP, Galushko SV, Svistunova NY, Avilov DV, Kuz'mina NA, Raevski NI, Struchkov YT, Pysarevsky AP, Belokon YN. General method for the synthesis of enantiomerically pure β-hydroxy-α-amino acids, containing fluorine atoms in the side chains. Case of stereochemical distinction between methyl and trifluoromethyl groups. X-Ray crystal and molecular structure of the nickel(II) complex of (2S,3S)-2(trifluoromethyl)threonine Journal of the Chemical Society-Perkin Transactions 1. 3143-3155. DOI: 10.1039/P19930003143 |
0.481 |
|
| 1993 |
Soloshonok VA, Kirilenko AG, Kukhar' VP, Resnati G. Transamination of fluorinated β-keto carboxylic esters. A biomimetic approach to β-polyfluoroalkyl-β-amino acids. Tetrahedron Letters. 34: 3621-3624. DOI: 10.1016/S0040-4039(00)73652-5 |
0.308 |
|
| 1993 |
Soloshonok VA, Svistunova NY, Skryma RN, Rybal'chenko VV, Kukhar VP, Luik AI, Belokon YN, Kuz'mina NA. Asymmetric synthesis of heteroorganic analogs of natural compounds. XVI. Asymmetric synthesis and study of the specific bioactivity of (2R,3S)- and (2S,3R)-2-amino-3-hydroxy-4-phosphonobutyric acids Pharmaceutical Chemistry Journal. 27: 644-647. DOI: 10.1007/BF00780587 |
0.324 |
|
| 1993 |
Soloshonok VA, Svistunova NY, Kukhar' VP, Kuz'mina NA, Popov VI, Belokon YN. Asymmetric synthesis of organoelement analogs of natural products Russian Chemical Bulletin. 42: 755-759. DOI: 10.1007/Bf00704021 |
0.424 |
|
| 1992 |
Basiuk VA, Gromovoy TY, Chuiko AA, Soloshonok VA, Kukhar VP. A Novel Approach to the Synthesis of Symmetric Optically Active 2,5-Dioxopiperazines Synthesis. 1992: 449-451. DOI: 10.1055/S-1992-26131 |
0.418 |
|
| 1992 |
Soloshonok V, Kukhar V, Pustovit Y, Nazaretian V. A New and Convenient Synthesis ofS-Trifluoromethyl-Containing Amino Acids Synlett. 1992: 657-658. DOI: 10.1055/S-1992-21447 |
0.498 |
|
| 1992 |
Soloshonok VA, Belokon YN, Kuzmina NA, Maleev VI, Svistunova NY, Solodenko VA, Kukhar VP. Asymmetric synthesis of phosphorus analogues of dicarboxylic α-amino acids Journal of the Chemical Society-Perkin Transactions 1. 1525-1529. DOI: 10.1039/P19920001525 |
0.568 |
|
| 1992 |
Soloshonok V, Svistunova N, Kukhar' V, Rozhenko A, Belokon' Y. General method for the asymmetric synthesis of fluorine-containing amino acids Journal of Fluorine Chemistry. 58: 368. DOI: 10.1016/S0022-1139(00)80834-9 |
0.531 |
|
| 1992 |
Bravo P, Frigerio M, Viani F, Soloshonok V, Cavicchio G. Asymmetric synthesis of trifluoro- and difluorochloro- methyl-containing epoxides Journal of Fluorine Chemistry. 58: 353. DOI: 10.1016/S0022-1139(00)80818-0 |
0.477 |
|
| 1992 |
Bravo P, Frigerio M, Viani F, Soloshonok V, Cavicchio G. The preparation and use of new fluorinated chirons Journal of Fluorine Chemistry. 58: 165. DOI: 10.1016/S0022-1139(00)80613-2 |
0.394 |
|
| 1992 |
Galushko S, Shishkina I, Soloshonok V. High-performance ligand-exchange chromatography of some amino acids containing two chiral centres Journal of Chromatography A. 592: 345-348. DOI: 10.1016/0021-9673(92)85106-4 |
0.402 |
|
| 1992 |
Soloshonok VA, Svistunova NY, Kukhar VP, Solodenko VA, Kuz'mina NA, Rozhenko AB, Galushko SV, Shishkina IP, Gudima AO, Belokon YN. Asymmetric synthesis of heteroorganic analogs of natural products. 6. (S)-α-amino-ω-phosphonocarboxylic acids Russian Chemical Bulletin. 41: 311-315. DOI: 10.1007/Bf00869521 |
0.521 |
|
| 1992 |
Soloshonok VA, Svistunova NY, Kukhar VP, Gudima AO, Kuz'mina NA, Belokon YN. Asymmetric synthesis of organoelemental analogs of natural compounds. 7. (2R,3S)-2-amino-3-hydroxy-5-phosphonovaleric acid Russian Chemical Bulletin. 41: 922-925. DOI: 10.1007/Bf00864540 |
0.517 |
|
| 1992 |
Soloshonok VA, Svistunova NY, Kukhar VP, Kuz'mina NA, Belokon YN. Asymmetrical synthesis of organometallic analogs of natural compounds. 8. Reactions of pentafluorobenzaldehyde with the Ni(II) complex of a schiff base of glycine and (S)-2-[N-(benzylprolyl)amino]benzophenone Russian Chemical Bulletin. 41: 540-545. DOI: 10.1007/Bf00863081 |
0.483 |
|
| 1991 |
Kukhar' VP, Soloshonok VA. Aliphatic fluorine-containing amino acids Russian Chemical Reviews. 60: 850-864. DOI: 10.1070/RC1991v060n08ABEH001115 |
0.346 |
|
| 1991 |
Soloshonok VA, Kukhar VP, Galushko SV, Rozhenko AB, Kuz'mina NA, Kolycheva MT, Belokon YN. Asymmetric synthesis of heteroorganic analogs of natural products 5. Synthesis of pure diastereomers and enantiomers of fluoro-substituted (2S,3R)- and (2R,3R)-β-phenylserines Russian Chemical Bulletin. 40: 1692-1699. DOI: 10.1007/Bf01172275 |
0.394 |
|
| 1991 |
Soloshonok VA, Kukhar VP, Galushko SV, Kolycheva MT, Rozhenko AB, Belokon YN. Asymmetric synthesis of heteroorganic analogs of natural compounds. 3. General preparative method of diastereo- and enantioselective synthesis of fluorine-containing 2(R), 3(S)-Β-phenylserines Russian Chemical Bulletin. 40: 1046-1054. DOI: 10.1007/Bf00961372 |
0.468 |
|
| 1991 |
Soloshonok VA, Kukhar VP, Batsanov AS, Galakhov MA, Belokon YN, Struchkov YT. Asymmetric synthesis of heteroorganic analogs of natural compounds. 4. Diastereo- and enantioselective synthesis of (2s, 3s)-4,4,4-trifluorothreonine and (2s, 3s)-β-perfluoroalkylserines Russian Chemical Bulletin. 40: 1366-1372. DOI: 10.1007/Bf00961234 |
0.404 |
|
| 1990 |
Soloshonok VA, Belokon YN, Kukhar VP, Chernoglazova NI, Saporovskaya MB, Bakhmutov VI, Kolycheva MT, Belikov VM. Asymmetric synthesis of heteroorganic analogs of natural compounds. 2. A convenient preparative method for the synthesis of enantiomerically pure (S)-(-)-o-, m-, and p-fluorophenylalanines and their 2-methylsubstituted analogs Russian Chemical Bulletin. 39: 1479-1485. DOI: 10.1007/Bf00957865 |
0.438 |
|
| 1990 |
KUKHAR' VP, YAGUPOL'SKII YL, SOLOSHONOK VA. ChemInform Abstract: β-Fluorosubstituted Amino Acids Cheminform. 21. DOI: 10.1002/chin.199020338 |
0.34 |
|
| 1990 |
SOLOSHONOK VA, YAGUPOL'SKII YL, KUKHAR' VP. ChemInform Abstract: Derivatives of α-Trifluoromethylmalic Acid and Their Reactions. Cheminform. 21. DOI: 10.1002/chin.199012111 |
0.403 |
|
| 1990 |
SOLOSHONOK VA, KHOTKEVICH AB, SERGUCHEV YA. ChemInform Abstract: Reaction of 3,7-Dimethylenebicyclo(3.3.1)nonane with the Pyridinium Salts of Perfluorocarboxylic Acids. Cheminform. 21. DOI: 10.1002/chin.199010132 |
0.342 |
|
| 1989 |
SOLOSHONOK VA, YAGUPOL'SKII YL, KUKHAR' VP. ChemInform Abstract: Fluorosubstituted Amino Acids. Part 5. Imines of Trifluoropyruvic Acid in the Synthesis of N-Substituted Trifluoroalanines. Cheminform. 20. DOI: 10.1002/chin.198902276 |
0.409 |
|
| 1988 |
SOLOSHONOK VA, GERUS II, YAGUPOL'SKII YL, KUKHAR' VP. ChemInform Abstract: Fluoroamino Acids. Part 3. α-Trifluoromethylamino Acids. Cheminform. 19. DOI: 10.1002/chin.198812104 |
0.365 |
|
| 1987 |
SOLOSHONOK VA, GERUS II, YAGUPOL'SKII YL, KUKHAR' VP. ChemInform Abstract: α-Trifluoromethyl-α-hydroxycarboxylic Acids. Cheminform. 18. DOI: 10.1002/chin.198748151 |
0.306 |
|
| 1986 |
SOLOSHONOK VA, GERUS II, YAGUPOL'SKII YL. ChemInform Abstract: N-(Methoxycarbonyl)imine of Trifluoropyrotartaric Acid. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198645140 |
0.309 |
|
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