Haghighi F, Jesikiewicz L, Stahl C, Nafie J, Ortega-Vega A, Liu P
J Am Chem Soc. 2024; 147(1):498-509.
PMID: 39702925
PMC: 11726561.
DOI: 10.1021/jacs.4c11661.
Lei B, Jiang W, Ma J, Wang C, Pan Y, Zhang Z
Biotechnol Lett. 2024; 47(1):11.
PMID: 39656280
DOI: 10.1007/s10529-024-03553-5.
Zhang X, Huang K, Fu Y, Zhang N, Kong X, Cheng Y
Nat Commun. 2024; 15(1):5881.
PMID: 38997250
PMC: 11245495.
DOI: 10.1038/s41467-024-49946-y.
Garg A, Rendina D, Bendale H, Akiyama T, Ojima I
Front Chem. 2024; 12:1398397.
PMID: 38783896
PMC: 11112575.
DOI: 10.3389/fchem.2024.1398397.
Yuan T, Ye X, Zhao P, Teng S, Yi Y, Wang J
Chem. 2024; 6(6):1420-1431.
PMID: 38250714
PMC: 10798669.
DOI: 10.1016/j.chempr.2020.03.014.
Asymmetric Ruthenium-Catalyzed Carbonyl Allylations by Gaseous Allene via Hydrogen Auto-Transfer: 1° vs 2° Alcohol Dehydrogenation for Streamlined Polyketide Construction.
Saludares C, Ortiz E, Santana C, Spinello B, Krische M
ACS Catal. 2023; 13(3):1662-1668.
PMID: 37869365
PMC: 10586519.
DOI: 10.1021/acscatal.2c05425.
A Simple Screening and Optimization Bioprocess for Long-Chain Peptide Catalysts Applied to Asymmetric Aldol Reaction.
Wang S, Teng H, Wang L, Li P, Yuan X, Sang X
Molecules. 2023; 28(19).
PMID: 37836827
PMC: 10574572.
DOI: 10.3390/molecules28196985.
Chemical reactivity of the tryptophan/acetone/DMSO triad system and its potential applications in nanomaterial synthesis.
Huang C, Liao H, Hu T
RSC Adv. 2023; 13(43):29802-29808.
PMID: 37829717
PMC: 10566338.
DOI: 10.1039/d3ra06596k.
A catalytic enantioselective stereodivergent aldol reaction.
Rahman M, Cellnik T, Ahuja B, Li L, Healy A
Sci Adv. 2023; 9(11):eadg8776.
PMID: 36921040
PMC: 10017038.
DOI: 10.1126/sciadv.adg8776.
Protected -Aldol Compounds from Direct, Catalytic, and Enantioselective Reactions of -Acyl-1,3-oxazinane-2-thiones with Aromatic Acetals.
Mellado-Hidalgo M, Romero-Cavagnaro E, Nageswaran S, Puddu S, Kennington S, Costa A
Org Lett. 2023; 25(4):659-664.
PMID: 36700336
PMC: 9903318.
DOI: 10.1021/acs.orglett.2c04254.
New boro amino amide organocatalysts for asymmetric cross aldol reaction of ketones with carbonyl compounds.
Begum Z, Seki C, Okuyama Y, Kwon E, Uwai K, Tokiwa M
RSC Adv. 2023; 13(2):888-894.
PMID: 36686933
PMC: 9811241.
DOI: 10.1039/d2ra06272k.
A simple protocol for determination of enantiopurity of amines using BINOL derivatives as chiral solvating agents H- and F-NMR spectroscopic analysis.
Chaudhary P, Yadav G, Singh S
RSC Adv. 2022; 12(39):25457-25464.
PMID: 36199308
PMC: 9453926.
DOI: 10.1039/d2ra05291a.
A Degenerate Metal-Templated Catalytic System with Redundant Functional Groups for the Asymmetric Aldol Reaction.
Sors-Vendrell A, Ortiz A, Meneses D, Alfonso I, Sola J, Jimeno C
J Org Chem. 2022; 87(11):7509-7513.
PMID: 35583468
PMC: 9171831.
DOI: 10.1021/acs.joc.2c00414.
Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions.
Sharifa Zaithun B, Emilia A, Mohamed Ibrahim Mohamed T, Karen Anne C, Mohd Basyaruddin A
RSC Adv. 2022; 8(59):34004-34011.
PMID: 35548802
PMC: 9086720.
DOI: 10.1039/c8ra06814c.
Direct and Asymmetric Aldol Reactions of N-Azidoacetyl-1,3-thiazolidine-2-thione Catalyzed by Chiral Nickel(II) Complexes. A New Approach to the Synthesis of β-Hydroxy-α-Amino Acids.
Teloxa S, Mellado-Hidalgo M, Kennington S, Romea P, Urpi F, Aullon G
Chemistry. 2022; 28(38):e202200671.
PMID: 35504848
PMC: 9401014.
DOI: 10.1002/chem.202200671.
Development of fructose-1,6-bisphosphate aldolase enzyme peptide mimics as biocatalysts in direct asymmetric aldol reactions.
Peme T, Brady D, Juma W, Makatini M
RSC Adv. 2022; 11(58):36670-36681.
PMID: 35494350
PMC: 9043830.
DOI: 10.1039/d1ra06616a.
Chiral proline-substituted porous organic cages in asymmetric organocatalysis.
Xu N, Su K, M El-Sayed E, Ju Z, Yuan D
Chem Sci. 2022; 13(12):3582-3588.
PMID: 35432868
PMC: 8943855.
DOI: 10.1039/d2sc00395c.
Comparison of mesoporous fractal characteristics of silica-supported organocatalysts derived from bipyridine-proline and resultant effects on the catalytic asymmetric aldol performances.
Xu G, Bing L, Jia B, Bai S, Sun J
RSC Adv. 2022; 12(17):10800-10814.
PMID: 35424978
PMC: 8988269.
DOI: 10.1039/d2ra00971d.
-Alkylation/aldol reaction of α-aldimino thioesters: a facile three-component coupling reaction.
Shimizu M, Higashino A, Mizota I, Zhu Y
RSC Adv. 2022; 11(22):13097-13104.
PMID: 35423863
PMC: 8697212.
DOI: 10.1039/d1ra02000e.
Synthesis of Atropisomeric Two-Axis Systems by the Catalyst-Controlled syn- and anti-Selective Arene-Forming Aldol Condensation.
Moser D, Sparr C
Angew Chem Int Ed Engl. 2022; 61(24):e202202548.
PMID: 35343034
PMC: 9322266.
DOI: 10.1002/anie.202202548.