Jayaraman Sivaguru
0000-0002-0446-6903
North Dakota State University
54 papers found
Refreshing results…
Enantiospecific 6π-photocyclization of atropisomeric α-substituted acrylanilides in the solid-state: role of crystalline confinement on enantiospecificity
Supramolecular photocatalysis: insights into cucurbit[8]uril catalyzed photodimerization of 6-methylcoumarin
Reactive spin state dependent enantiospecific photocyclization of axially chiral α-substituted acrylanilides
Controlling photoreactions through non-covalent interactions within zeolite nanocages
Decoding Stereocontrol During the Photooxygenation of Oxazolidinone-Functionalized Enecarbamates
Supramolecular photocatalysis by confinement - Photodimerization of coumarins within cucurbit[8]urils
Photochemical type II reaction of atropchiral benzoylformamides to point chiral oxazolidin-4-ones. Axial chiral memory leading to enantiomeric resolution of photoproducts
Enantiospecific Photochemical Norrish/Yang Type II Reaction of Nonbiaryl Atropchiral α-Oxoamides in Solution—Axial to Point Chirality Transfer
Isolation and syn Elimination of a Peterson Adduct to Obtain Optically Pure Product in the Diastereoselective Synthesis of Oxazolidinone- Functionalized Enecarbamates
Light-Induced Transfer of Molecular Chirality in Solution: Enantiospecific Photocyclization of Molecularly Chiral Acrylanilides
6π-Photocyclization of O-tert-butylacrylanilides. N-substitution dictates the regiochemistry of cyclization
Physical and chemical quenching rates and their influence on stereoselective photooxygenation of oxazolidinone-functionalized enecarbamates
Manipulating Photochemical Reactivity of Coumarins within Cucurbituril Nanocavities
Photodimerization and complexation dynamics of coumarins in the presence of cucurbit[8]urils
Vibrational deactivation of singlet oxygen: Does it play a role in stereoselectivity during photooxygenation?
Controlled diastereoselectivity at the alkene-geometry through selective encapsulation: E-Zphotoisomerization of oxazolidinone-functionalized enecarbamates within hydrophobic nano-cavities
A comparative mechanistic analysis of the stereoselectivity trends observed in the oxidation of chiral oxazolidinone-functionalized enecarbamates by singlet oxygen, ozone, and triazolinedione
Conformationally controlled (entropy effects), stereoselective vibrational quenching of singlet oxygen in the oxidative cleavage of oxazolidinone-functionalized enecarbamates through solvent and temperature variations
Control of Chirality by Cations in Confined Spaces: Photooxidation of Enecarbamates Inside Zeolite Supercages
Chiral Photochemistry Within Zeolites
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