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Three Chiral sentence examples within three chiral carbon



Asymmetric Cycloetherification of in Situ Generated Cyanohydrins through the Concomitant Construction of Three Chiral Carbon Centers.



Enantioselective Copper-Catalyzed Desymmetrization of 1,3-Diketones Involving Borylation of Styrenes.


Three Chiral sentence examples within three chiral center



Reconfigurable Chiral Plasmonics beyond Single Chiral Centers.



Highly Enantioselective Iridium-Catalyzed Cascade Double Allylation Strategy: Synthesis of Pyrrolidinoindolines with an All-Carbon Quaternary Stereocenter.


Three Chiral sentence examples within three chiral multiplet



Uplifting Anti-D6-brane



Superconformal generalizations of auxiliary vector modified polynomial f(R) theories.



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Cycloaddition Reactions of Sugar-Based Olefins, Nitrones and Nitrile Oxides: En Route to Saccharidic Spiroisoxazoli(di)nes


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10.1021/acs.jpca.9b03864

Basis Set Superposition Errors in the Many-Body Expansion of Molecular Properties.


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10.1142/9789811210679_0018

Anomalies and Bose symmetry


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10.1021/acs.orglett.9b00462

Asymmetric Cycloetherification of in Situ Generated Cyanohydrins through the Concomitant Construction of Three Chiral Carbon Centers.


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10.1021/acsnano.9b09179

Reconfigurable Chiral Plasmonics beyond Single Chiral Centers.


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10.1002/elps.201800471

The degree of substitution affects the enantioselectivity of sulfobutylether‐β‐cyclodextrin chiral stationary phases


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10.1007/JHEP12(2019)171

Uplifting Anti-D6-brane


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10.1021/acs.inorgchem.9b02044

Gadolinium Complexes of Highly Rigid, Open-Chain Ligands Containing a Cyclobutane Ring in the Backbone: Decreasing Ligand Denticity Might Enhance Kinetic Inertness.


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10.1016/j.toxlet.2019.12.004

Screening of chiral shift reagents suitable to generically separate the enantiomers of V-agents by 31P-NMR spectroscopy.


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10.1103/PhysRevLett.122.072001

Relating Hadronic CP Violation to Higher-Twist Distributions.


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10.17344/ACSI.2018.4790

Three chiral cyanide-bridged Cr–Cu complexes: Synthesis, crystal structures and magnetic properties


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10.1103/PhysRevD.101.015004

Gauging the accidental symmetries of the Standard Model, and implications for the flavour anomalies.


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10.1002/anie.201914042

A Unified Total Synthesis of the Actinoallolides, a Family of Potent Anti-trypanosomal Macrolides.


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10.1021/acs.orglett.9b03382

Highly Enantioselective Iridium-Catalyzed Cascade Double Allylation Strategy: Synthesis of Pyrrolidinoindolines with an All-Carbon Quaternary Stereocenter.


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10.1021/acs.orglett.9b02199

Enantioselective Copper-Catalyzed Desymmetrization of 1,3-Diketones Involving Borylation of Styrenes.


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10.1002/anie.201908959

Chiral Phosphoric Acids in Metal-Organic Frameworks with Enhanced Acidity and Tunable Catalytic Selectivity.


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10.1002/anie.201909929

Synthesis of Chiral Tetrasubstituted Azetidines from Donor-Acceptor Azetines via Asymmetric Copper(I)-Catalyzed Imido-Ylide [3+1]-Cycloaddition with Metallo-Enolcarbenes.


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10.1002/chem.201902676

Precise Manipulation of Temperature-Driven Chirality Switching of Molecular Universal Joints through Solvent Mixing.


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10.1002/anie.201910898

Asymmetric Synthesis of Oxa-Bridged Oxazocines by Rh(II)/Zn(II) Relay Catalytic [4+3] Cycloaddition Reaction.



Supramolecular chirality transformation driven by monodentate ligand binding to a coordinatively unsaturated self-assembly based on C 3-symmetric ligands.


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10.1088/1475-7516/2020/04/005

Superconformal generalizations of auxiliary vector modified polynomial f(R) theories.


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10.1103/physreve.100.052704

Elucidation of the de Vries behavior in terms of the orientational order parameter, apparent tilt angle, and field-induced tilt angle for smectic liquid crystals by polarized infrared spectroscopy.


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10.1103/PhysRevD.99.095029

Origin of Yukawa couplings for Higgs and leptoquarks.


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10.1103/PhysRevD.99.075008

Minimal radiative Dirac neutrino mass models


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10.1016/j.physletb.2019.134837

A perturbative study of holographic mABJM theory


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10.1002/anie.201902565

Reversing the Handedness of Self-Assembled Porous Molecular Networks through the Number of Identical Chiral Centres.


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