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Noor-ul H. Khan

Researcher at Central Salt and Marine Chemicals Research Institute

Publications -  224
Citations -  5151

Noor-ul H. Khan is an academic researcher from Central Salt and Marine Chemicals Research Institute. The author has contributed to research in topics: Catalysis & Enantioselective synthesis. The author has an hindex of 36, co-authored 224 publications receiving 4615 citations. Previous affiliations of Noor-ul H. Khan include Charotar University of Science and Technology & Council of Scientific and Industrial Research.

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Chiral Mn(III) salen complexes covalently bonded on modified MCM-41 and SBA-15 as efficient catalysts for enantioselective epoxidation of nonfunctionalized alkenes

TL;DR: In this paper, a chiral Mn(III) salen complex supported onto modified mesoporous supports (MCM-41 and SBA-15) was prepared using 3-aminopropyltriethoxysilane as a reactive surface modifier by a covalent grafting method.
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Metal catalyzed asymmetric cyanation reactions

TL;DR: In this article, the authors discuss the various methods for catalytic asymmetric synthesis of cyanohydrins derived from both aldehydes and ketones using different sources of cyanide.
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Synthesis, characterization, and EPR studies of stable ruthenium(III) Schiff base chloro and carbonyl complexes

TL;DR: In this paper, the oxidation state of the metal ion in these complexes is confirmed to be +3 by electrochemical, magnetic susceptibility, and EPR measurements using elemental analysis and IR, UV-visible, differential-pulse polarography.
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Dicationic chiral Mn(III) salen complex exchanged in the interlayers of montmorillonite clay: a heterogeneous enantioselective catalyst for epoxidation of nonfunctionalized alkenes

TL;DR: In this article, a chiral MnIII salen complexes 1−4 were obtained from the reaction of 1S,2S-(+)-1,2-diaminocyclohexane/1S, 2S-(−)-diphenyldiamine with 2-hydroxy-3-t-Bu-5-(triisooctylaminomethyl) benzaldehyde chloride/2-hydroxyl-3t-bu-5-branched-benzaldehyde chloride and were exchanged in montmorillonite clay
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Enantioselective epoxidation of non-functionalised alkenes using a urea–hydrogen peroxide oxidant and a dimeric homochiral Mn(III)-Schiff base complex catalyst

TL;DR: The catalytic enantioselective epoxidation of chromenes, indene and styrene using a urea-hydrogen peroxide adduct as an oxidising agent and the novel dimeric homochiral Mn(III)-Schiff base catalyst 1 has been investigated in the presence of carboxylate salts and nitrogen and oxygen coordinating co-catalysts as mentioned in this paper.