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Dive into the research topics where Suleman M. Inamdar is active.

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Featured researches published by Suleman M. Inamdar.


RSC Advances | 2012

Efficient, rapid synthesis of bis(indolyl)methane using ethyl ammonium nitrate as an ionic liquid

Shafeek A. R. Mulla; A. Sudalai; Mohsinkhan Y. Pathan; Shafi A. Siddique; Suleman M. Inamdar; Santosh S. Chavan; R. Santosh Reddy

A simple and rapid protocol has been developed for an efficient synthesis of bis(indolyl)methane in excellent yields using ethyl ammonium nitrate (EAN) as reusable ionic liquid at room temperature. The protocol involves an electrophilic substitution reaction of indoles with several aldehydes.


RSC Advances | 2015

Ligand-, base-, co-catalyst-free copper fluorapatite (CuFAP) as a versatile, ecofriendly, heterogeneous and reusable catalyst for an efficient homocoupling of arylboronic acid at ambient reaction conditions

Shafeek A. R. Mulla; Santosh S. Chavan; Mohsinkhan Y. Pathan; Suleman M. Inamdar; Taufeekaslam M. Y. Shaikh

This paper describes the first report in which copper species containing copper fluorapatite (CuFAP) acts as a versatile, eco-friendly, recyclable, heterogeneous catalyst for an efficient synthesis of symmetric biaryls from the homo-coupling of arylboronic acids in methanol solvent at ambient reaction conditions. The developed protocol is ligand-, base-, and co-catalyst-free, sustainable, mild, inexpensive, and compatible with a wide range of aromatic/heterocyclic boronic acids and provides the corresponding products in excellent yields without purification. The catalyst was easily recovered from the reaction mixture and reused several times without loss of activity.


RSC Advances | 2012

Base promoted highly efficient copper fluorapatite catalyzed coupling of phenols with arylboronic acids under mild and ligand -free conditions

Shafeek A. R. Mulla; Suleman M. Inamdar; Mohsinkhan Y. Pathan; Santosh S. Chavan

A mild, general and highly efficient protocol has been developed for the synthesis of diaryl ethers in good to excellent yield under mild and ligand-free conditions. This is the first example in which a recyclable, heterogeneous copper fluorapatite catalyst is used for the arylation of phenols with arylboronic acids at room temperature in the presence of Cs2CO3 as a base and methanol as a solvent. The catalyst was recovered and reused several times without loss of catalytic activity.


Organic chemistry frontiers | 2015

Engineering ligands on the Au center: discovering broadly applicable gold catalysis with high turnover numbers

Suleman M. Inamdar; Nitin T. Patil

The research groups of Hammond/Xu and Zhang report the discovery of new ligands for gold catalysis. With these ligands, gold catalyzed reactions have been reported for a broader range of substrates with very high TONs at a level that can match the needs of large-scale applications.


Chemical Communications | 2017

[3+2]-Annulation of platinum-bound azomethine ylides with distal CC bonds of N-allenamides

Indradweep Chakrabarty; Suleman M. Inamdar; Manjur O. Akram; Amol B. Gade; Subhrashis Banerjee; Saibal Bera; Nitin T. Patil

A Pt-catalyzed, highly regioselective reaction between N-allenamides and imino-alkynes leading to pyrrolo[1,2-a]indoles is described. This represents the first example of [3+2]-annulation of Pt-bound azomethine ylides with the distal C[double bond, length as m-dash]C bond of N-allenamides. The mechanism of the reaction was established by computational studies.


RSC Advances | 2016

A unified approach to pyrrole-embedded aza-heterocyclic scaffolds based on the RCM/isomerization/cyclization cascade catalyzed by a Ru/B-H binary catalyst system

Suleman M. Inamdar; Indradweep Chakrabarty; Nitin T. Patil

An easy and straightforward preparation of pyrrole-embedded aza-heterocyclic scaffolds employing a Ru/B-H binary catalyst system has been developed. The strategy generates a diverse array of privileged scaffolds from 2-aminophenyl group appended pyrroles that can be prepared by a two-step process from corresponding aminoaryl-substituted pyrroles. The technique of incorporating 2-aminoaromatic groups in the heterocycles and their subsequent ring-closing-metathesis (RCM) isomerization followed by subsequent Pictet–Spengler type reaction should also be applicable to other heterocycles for generating a library of multi-ring compounds in an efficient manner.


Tetrahedron Letters | 2013

CuO nano-particles supported on silica, a new catalyst for facile synthesis of benzimidazoles, benzothiazoles and benzoxazoles

Suleman M. Inamdar; Vinod K. More; Sisir K. Mandal


Organic and Biomolecular Chemistry | 2015

Enantioselective cooperative catalysis

Suleman M. Inamdar; Valmik S. Shinde; Nitin T. Patil


Chemical Communications | 2014

When gold meets chiral Brønsted acid catalysts: extending the boundaries of enantioselective gold catalysis

Suleman M. Inamdar; Ashok Konala; Nitin T. Patil


Tetrahedron Letters | 2012

Ligand free, highly efficient synthesis of diaryl ether over copper fluorapatite as heterogeneous reusable catalyst

Shafeek A. R. Mulla; Suleman M. Inamdar; Mohsinkhan Y. Pathan; Santosh S. Chavan

Collaboration


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Mohsinkhan Y. Pathan

Academy of Scientific and Innovative Research

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Nitin T. Patil

Council of Scientific and Industrial Research

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Santosh S. Chavan

Academy of Scientific and Innovative Research

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Shafeek A. R. Mulla

Academy of Scientific and Innovative Research

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Indradweep Chakrabarty

Council of Scientific and Industrial Research

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Amol B. Gade

Academy of Scientific and Innovative Research

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Ashok Konala

Council of Scientific and Industrial Research

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Manjur O. Akram

Council of Scientific and Industrial Research

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Rajesh G. Gonnade

Council of Scientific and Industrial Research

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Saibal Bera

Council of Scientific and Industrial Research

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