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Items: 1 to 20 of 97

1.

Large-Scale Asymmetric Synthesis of Fmoc-(S)-2-Amino-6,6,6-Trifluorohexanoic Acid.

Yin Z, Moriwaki H, Abe H, Miwa T, Han J, Soloshonok VA.

ChemistryOpen. 2019 Jun 7;8(6):701-704. doi: 10.1002/open.201900131. eCollection 2019 Jun.

2.

Fluorine-Containing Drugs Approved by the FDA in 2018.

Mei H, Han J, Fustero S, Medio-Simon M, Sedgwick DM, Santi C, Ruzziconi R, Soloshonok VA.

Chemistry. 2019 May 17. doi: 10.1002/chem.201901840. [Epub ahead of print] Review.

PMID:
31099931
3.

Optical Resolution of Rimantadine.

Han J, Takeda R, Sato T, Moriwaki H, Abe H, Izawa K, Soloshonok VA.

Molecules. 2019 May 12;24(9). pii: E1828. doi: 10.3390/molecules24091828.

4.

Effect of substituents on the configurational stability of the stereogenic nitrogen in metal(II) complexes of α-amino acid Schiff bases.

Mei H, Jean M, Albalat M, Vanthuyne N, Roussel C, Moriwaki H, Yin Z, Han J, Soloshonok VA.

Chirality. 2019 May;31(5):401-409. doi: 10.1002/chir.23066. Epub 2019 Mar 27.

PMID:
30916841
5.

The self-disproportionation of enantiomers (SDE) of amino acids and their derivatives.

Han J, Wzorek A, Kwiatkowska M, Soloshonok VA, Klika KD.

Amino Acids. 2019 Jun;51(6):865-889. doi: 10.1007/s00726-019-02729-y. Epub 2019 Mar 22. Review.

PMID:
30903285
6.

Chromatographic approach to study the configurational stability of Ni(II) complexes of amino-acid Schiff bases possessing stereogenic nitrogen.

Han J, Jean M, Roussel C, Moriwaki H, Soloshonok VA.

Chirality. 2019 Apr;31(4):328-335. doi: 10.1002/chir.23059. Epub 2019 Jan 31.

PMID:
30702773
7.

The self-disproportionation of enantiomers (SDE): The effect of scaling down, potential problems versus prospective applications, possible new occurrences, and unrealized opportunities?

Han J, Wzorek A, Soloshonok VA, Klika KD.

Electrophoresis. 2019 Jan 17. doi: 10.1002/elps.201800414. [Epub ahead of print] Review.

PMID:
30653701
8.

Chemistry of detrifluoroacetylatively in situ generated fluoro-enolates.

Mei H, Liu J, Fustero S, Román R, Ruzziconi R, Soloshonok VA, Han J.

Org Biomol Chem. 2019 Jan 23;17(4):762-775. doi: 10.1039/c8ob02843e. Review.

PMID:
30574988
9.

Asymmetric synthesis of (2S,3S)-3-Me-glutamine and (R)-allo-threonine derivatives proper for solid-phase peptide coupling.

Tokairin Y, Soloshonok VA, Moriwaki H, Konno H.

Amino Acids. 2019 Mar;51(3):419-432. doi: 10.1007/s00726-018-2677-5. Epub 2018 Nov 17.

PMID:
30449004
10.

Mannich-type addition of 1,3-dicarbonyl compounds to chiral tert-butanesulfinyltrifluoroacetaldimines. Mechanistic aspects and chiroptical studies.

Mazzeo G, Longhi G, Abbate S, Mangiavacchi F, Santi C, Han J, Soloshonok VA, Melensi L, Ruzziconi R.

Org Biomol Chem. 2018 Nov 21;16(45):8742-8750. doi: 10.1039/c8ob02204f.

PMID:
30393798
11.

The self-disproportionation of enantiomers (SDE) of α-amino acid derivatives: facets of steric and electronic properties.

Hosaka T, Imai T, Wzorek A, Marcinkowska M, Kolbus A, Kitagawa O, Soloshonok VA, Klika KD.

Amino Acids. 2019 Feb;51(2):283-294. doi: 10.1007/s00726-018-2664-x. Epub 2018 Oct 11.

PMID:
30311082
12.
13.

Second-order asymmetric transformation and its application for the practical synthesis of α-amino acids.

Takeda R, Kawamura A, Kawashima A, Sato T, Moriwaki H, Izawa K, Abe H, Soloshonok VA.

Org Biomol Chem. 2018 Jul 11;16(27):4968-4972. doi: 10.1039/c8ob00963e.

PMID:
29947401
14.

Palladium-Catalyzed Asymmetric Allylic Alkylations of Colby Pro-Enolates with MBH Carbonates: Enantioselective Access to Quaternary C-F Oxindoles.

Zhu Y, Mao Y, Mei H, Pan Y, Han J, Soloshonok VA, Hayashi T.

Chemistry. 2018 Jun 26;24(36):8994-8998. doi: 10.1002/chem.201801670. Epub 2018 May 24.

PMID:
29683211
15.

The self-disproportionation of enantiomers (SDE): a menace or an opportunity?

Han J, Kitagawa O, Wzorek A, Klika KD, Soloshonok VA.

Chem Sci. 2018 Jan 15;9(7):1718-1739. doi: 10.1039/c7sc05138g. eCollection 2018 Feb 21. Review.

16.

Modern Approaches for Asymmetric Construction of Carbon-Fluorine Quaternary Stereogenic Centers: Synthetic Challenges and Pharmaceutical Needs.

Zhu Y, Han J, Wang J, Shibata N, Sodeoka M, Soloshonok VA, Coelho JAS, Toste FD.

Chem Rev. 2018 Apr 11;118(7):3887-3964. doi: 10.1021/acs.chemrev.7b00778. Epub 2018 Apr 2.

17.

Axially chiral Ni(II) complexes of α-amino acids: Separation of enantiomers and kinetics of racemization.

Zhang W, Ekomo RE, Roussel C, Moriwaki H, Abe H, Han J, Soloshonok VA.

Chirality. 2018 Apr;30(4):498-508. doi: 10.1002/chir.22815. Epub 2018 Jan 23.

PMID:
29359493
18.

Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome.

Han J, Soloshonok VA, Klika KD, Drabowicz J, Wzorek A.

Chem Soc Rev. 2018 Feb 21;47(4):1307-1350. doi: 10.1039/c6cs00703a. Epub 2017 Dec 22.

PMID:
29271432
19.

Chemoselective SN2' Allylations of Detrifluoroacetylatively In Situ Generated 3-Fluoroindolin-2-one-Derived Tertiary Enolates with Morita-Baylis-Hillman Carbonates.

Zhu Y, Mei H, Han J, Soloshonok VA, Zhou J, Pan Y.

J Org Chem. 2017 Dec 15;82(24):13663-13670. doi: 10.1021/acs.joc.7b02409. Epub 2017 Dec 6.

PMID:
29178786
20.

Asymmetric synthesis of α-deuterated α-amino acids.

Takeda R, Abe H, Shibata N, Moriwaki H, Izawa K, Soloshonok VA.

Org Biomol Chem. 2017 Aug 23;15(33):6978-6983. doi: 10.1039/c7ob01720k.

PMID:
28792052

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