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Dive into the research topics where Anil Saini is active.

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Featured researches published by Anil Saini.


Synthetic Communications | 2007

RuCl3 · xH2O: A New Efficient Catalyst for Facile Preparation of 1,1‐Diacetates from Aldehydes

Anil Saini; Sanjay Kumar; Jagir S. Sandhu

Abstract An efficient, facile preparation of aldehyde 1,1‐diacetates (acylals) in excellent yields catalyzed by RuCl3 · xH2O is described. Ketones do not react under these conditions.


Synthetic Communications | 2007

New Strategy for the Oxidation of Hantzsch 1,4‐Dihydropyridines and Dihydropyrido[2,3‐d]pyrimidines Catalyzed by DMSO under Aerobic Conditions

Anil Saini; Sanjay Kumar; Jagir S. Sandhu

Abstract A novel metal‐salt‐oxidant‐free, efficient, and economical method for the oxidation of Hantzsch 1,4‐dihydropyridines that uses aerial oxygen and solvent‐grade dimethylsulfoxide is described. Also, the synthesis of pyrido[2,3‐d]pyrimidines is achieved from in situ oxidation of dihydropyrido[2,3‐d]pyrimidines that arise from the reaction of 6‐aminouracils and cyano olefins in dimethylsulfoxide.


Green Chemistry Letters and Reviews | 2009

Multicomponent eco-friendly synthesis of 3,4-dihydropyrimidine-2-(1H)-ones using an organocatalyst Lactic acid

Suresh; Anil Saini; Dhruva Kumar; Jagir S. Sandhu

Abstract Biginelli compounds 3,4-dihydropyrimidine-2-(1H)-ones are synthesized in high yields via eco-friendly simple reaction procedure using Lactic acid: organocatalyst. The new method reported herein is green and is free of formation of any hazardous by products. The process has significant advantages over other reported methods.


Synthetic Communications | 2008

RuCl3·xH2O: A Novel and Efficient Catalyst for the Facile Synthesis of 1,5-Benzodiazepines Under Solvent-Free Conditions

Suresh; Anil Saini; Jagir S. Sandhu

Abstract 1,5-Benzodizepines are synthesized in excellent yields via condensation of o-phenylenediamine with ketones having a hydrogen at the α-position. The reaction is performed in solvent-free conditions and 5 mol% of RuCl3·xH2O is enough to direct the reaction to completion.


Synthetic Communications | 2007

Iron(III) Chloride-Promoted, Solvent-Free, Facile, and Efficient Friedländer Synthesis of Quinolines

Sanjay Kumar; Anil Saini; Jagir S. Sandhu

Abstract A mild, efficient, and solvent‐free version of Friedländer annulation of 2‐amino ketones and α‐methylene carbonyl compounds for the synthesis of polysubstituted quinolines using a catalytic amount of commercially available iron(III) chloride at room temperature in excellent yields is described.


Journal of Scientific & Industrial Research | 2008

Hantzsch reaction: Recent advances in Hantzsch 1,4-dihydropyridines

Anil Saini; Sanjay Kumar; Jagir S. Sandhu


Synlett | 2006

A New LiBr-Catalyzed, Facile and Efficient Method for the Synthesis of 14-Alkyl or Aryl-14H-dibenzo[a,j]xanthenes and Tetrahydrobenzo[b]pyrans under Solvent-Free Conventional and Microwave Heating

Anil Saini; Sanjay Kumar; Jagir S. Sandhu


Tetrahedron Letters | 2005

A general method for the deoxygenation of aromatic N-oxides using RuCl3·xH2O

Sanjay Kumar; Anil Saini; Jagir S. Sandhu


Arkivoc | 2007

LiBr-mediated, solvent free von Pechmann reaction: facile and efficient method for the synthesis of 2H-chromen-2-ones

Sanjay Kumar; Anil Saini; Jagir S. Sandhu


Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry | 2007

Aluminium(III) halides mediated synthesis of 5-unsustituted 3,4-dihydropyrimidin-2(1H)-ones via three component Biginelli-like reaction

Anil Saini; Sanjay Kumar; Jagir S. Sandhu

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