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Density Functional Theory Mechanistic Study of the Regioselectivity of 1,3-Dipolar Cycloaddition Reaction Between Acyclic Nitrones and Norsarkomycin and Its Analogues

MOJ Drug Design Development & Therapy

doi 10.15406/mojddt.2017.01.00013

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August 24, 2017

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Density Functional Theory Mechanistic Study of the Regioselectivity of 1,3-Dipolar Cycloaddition Reaction Between Acyclic Nitrones and Norsarkomycin and Its Analogues

MOJ Drug Design Development & Therapy

doi 10.15406/mojddt.2017.01.00013

Full Text

Abstract

Date

Authors

Publisher

Related search

Ultrasonic Synthesis, Molecular Structure and Mechanistic Study of 1,3-Dipolar Cycloaddition Reaction of 1-Alkynylpyridinium-3-Olate and Acetylene Derivatives

Double 1,3-Dipolar Cycloaddition Reaction of 3-Phenylsydnone With 1,3-Dienes

The Regioselective Effect of the Allylic Silicon or Oxygen Atom in 1,3-Dipolar Cycloaddition of Nitrones

Synthesis of Oxetane/Azetidine Containing Spirocycles via the 1,3-Dipolar Cycloaddition Reaction

Α,β-Unsaturated Amides as Dipolarophiles: Catalytic Asymmetric Exo -Selective 1,3-Dipolar Cycloaddition With Nitrones

Α,β-Unsaturated Amides as Dipolarophiles: Catalytic Asymmetric Exo -Selective 1,3-Dipolar Cycloaddition With Nitrones

Strain-Promoted 1,3-Dipolar Cycloaddition of Cycloalkynes and Organic Azides

Mechanistic Investigation on the Reaction of O− With CH3CN Using Density Functional Theory

Synthesis and Characterization of 5-Substituted Novel Isoxazolidines Derived From 1,3-Dipolar Cycloaddition of Nitrones With Olefins: Studies of Antibacterial and Antifungal Activities.