Detalhe da pesquisa
1.
A Comparison of a Direct Electron Detector and a High-Speed Video Camera for a Scanning Precession Electron Diffraction Phase and Orientation Mapping.
Microsc Microanal
; 26(6): 1110-1116, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32867871
2.
A Facile Synthesis of Blue Luminescent [7]Helicenocarbazoles Based on Gold-Catalyzed Rearrangement-Iodonium Migration and Suzuki-Miyaura Benzannulation Reactions.
Chemistry
; 24(30): 7620-7625, 2018 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-29572999
3.
Photoinduced Gold-Catalyzed Domino C(sp) Arylation/Oxyarylation of TMS-Terminated Alkynols with Arenediazonium Salts.
J Org Chem
; 82(4): 2177-2186, 2017 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28150493
4.
Chemoenzymatic asymmetric synthesis of 1,4-benzoxazine derivatives: application in the synthesis of a levofloxacin precursor.
J Org Chem
; 80(8): 3815-24, 2015 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-25786159
5.
Vinylation of Unprotected Phenols Using a Biocatalytic System.
Angew Chem Int Ed Engl
; 54(37): 10899-902, 2015 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26227171
6.
Biocontrolled formal inversion or retention of L-α-amino acids to enantiopure (R)- or (S)-hydroxyacids.
Chemistry
; 20(35): 11225-8, 2014 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-25048982
7.
Chiral triazolium salts and ionic liquids: from the molecular design vectors to their physical properties through specific supramolecular interactions.
Chemistry
; 19(3): 892-904, 2013 Jan 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23197418
8.
Asymmetric chemoenzymatic synthesis of ramatroban using lipases and oxidoreductases.
J Org Chem
; 77(10): 4842-8, 2012 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22515546
9.
Stereoselective synthesis of 2,3-disubstituted indoline diastereoisomers by chemoenzymatic processes.
J Org Chem
; 77(18): 8049-55, 2012 Sep 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-22917174
10.
Characterization of hexacationic imidazolium ionic liquids as effective and highly stable gas chromatography stationary phases.
J Sep Sci
; 35(2): 273-9, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22162278
11.
Chemoenzymatic asymmetric synthesis of optically active pentane-1,5-diamine fragments by means of lipase-catalyzed desymmetrization transformations.
J Org Chem
; 76(14): 5709-18, 2011 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21627134
12.
Asymmetric chemoenzymatic synthesis of miconazole and econazole enantiomers. The importance of chirality in their biological evaluation.
J Org Chem
; 76(7): 2115-22, 2011 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21384803
13.
Evaluation of new ionic liquids as high stability selective stationary phases in gas chromatography.
Anal Bioanal Chem
; 400(5): 1209-16, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21188580
14.
Hydrolases: catalytically promiscuous enzymes for non-conventional reactions in organic synthesis.
Chem Soc Rev
; 39(11): 4504-23, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20877864
15.
From salts to ionic liquids by systematic structural modifications: a rational approach towards the efficient modular synthesis of enantiopure imidazolium salts.
Chemistry
; 16(3): 836-47, 2010 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-19946902
16.
Computational study of the lipase-mediated desymmetrisation of 2-substituted-propane-1,3-diamines.
Chembiochem
; 10(18): 2875-83, 2009 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-19885896
17.
Chemoenzymatic synthesis of rivastigmine based on lipase-catalyzed processes.
J Org Chem
; 74(15): 5304-10, 2009 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-19555095
18.
Enzymatic desymmetrization of prochiral 2-substituted-1,3-diamines: preparation of valuable nitrogenated compounds.
J Org Chem
; 74(6): 2571-4, 2009 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-19284738
19.
Hydrolases in the stereoselective synthesis of N-heterocyclic amines and amino acid derivatives.
Chem Rev
; 111(7): 3998-4035, 2011 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-21526748
20.
First desymmetrization of 1,3-propanediamine derivatives in organic solvent. Development of a new route for the preparation of optically active amines.
Org Lett
; 9(21): 4203-6, 2007 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-17880228