0000000001317439

AUTHOR

Nisshanth Raj Dharmaraj

showing 3 related works from this author

Regio‐, Diastereo‐, and Enantioselective Organocatalytic Addition of 4‐Substituted Pyrazolones to Isatin‐Derived Nitroalkenes

2019

Hydroquinine 2,5‐diphenyl‐4,6‐pyrimidinediyl diether [(DHQ)2Pyr] catalyzed the regio‐, diastereo‐, and enantioselective addition of 4‐substituted pyrazolones to isatin‐derived nitroalkenes, providing a variety of chiral alkenylpyrazolone adducts containing a tetrasubstituted stereocenter bearing an oxindole moiety with excellent yields, regioselectivity, and diastereoselectivity, as well as a moderate enantioselectivity (up to 98 % yield, > 20:1 E/Z ratio dr and 78 % ee). The reaction harnesses a nitroalkene as an alkenylating agent through a Nucleophilic Vinylic Substitution (SNV) reaction.

CatàlisiQuímica orgànica
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Regio-, Diastereo-, and Enantioselective Organocatalytic Addition of 4-Substituted Pyrazolones to Isatin-Derived Nitroalkenes

2019

"This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving."

010405 organic chemistryIsatinOrganic ChemistryEnantioselective synthesis010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryOrganocatalysisNucleophilic substitutionOrganic chemistryPyrazolonesPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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CCDC 1899761: Experimental Crystal Structure Determination

2019

Related Article: Carlos Vila, Nisshanth Raj Dharmaraj, Antonio Faubel, Gonzalo Blay, M. Luz Cardona, M. Carmen Muñoz, Jose R. Pedro|2019|Eur.J.Org.Chem.|2019|3040|doi:10.1002/ejoc.201900328

Space GroupCrystallography3-[(34-dimethyl-5-oxo-1-phenyl-45-dihydro-1H-pyrazol-4-yl)methylidene]-1-(prop-2-en-1-yl)-13-dihydro-2H-indol-2-oneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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