meta-Chloroperbenzoic acid (mCPBA): a versatile reagent in organic synthesis
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β2, 2 -Amino Acid N-Carboxyanhydrides Relying on Sequential Enantioselective C(4)-Functionalization of Pyrrolidin-2,3-diones and Regioselective Baeyer-Villiger Oxidation.Formation of δ-Lactones with anti-Baeyer-Villiger Regiochemistry: Investigations into the Mechanism of the Cerium-Catalyzed Aerobic Coupling of β-Oxoesters with Enol Acetates.Strategic design of a ruthenium catalyst for both CO2 reduction and H2O oxidation: the electronic influence of the co-ligands.Stereoselective Alkane Oxidation with meta-Chloroperoxybenzoic Acid (MCPBA) Catalyzed by Organometallic Cobalt Complexes.ChemInform Abstract: meta-Chloroperbenzoic Acid (mCPBA): A Versatile Reagent in Organic Synthesis
P2860
meta-Chloroperbenzoic acid (mCPBA): a versatile reagent in organic synthesis
description
article
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im Jahr 2014 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована у 2014
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name
meta-Chloroperbenzoic acid (mCPBA): a versatile reagent in organic synthesis
@en
meta-Chloroperbenzoic acid
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type
label
meta-Chloroperbenzoic acid (mCPBA): a versatile reagent in organic synthesis
@en
meta-Chloroperbenzoic acid
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prefLabel
meta-Chloroperbenzoic acid (mCPBA): a versatile reagent in organic synthesis
@en
meta-Chloroperbenzoic acid
@nl
P2093
P2860
P356
P1433
P1476
meta-Chloroperbenzoic acid (mCPBA): a versatile reagent in organic synthesis
@en
P2093
Ahmed Al-Harrasi
Ghulam Abbas
Hidayat Hussain
Ishtiaq Ahmed
Ivan R. Green
Najeeb Ur Rehman
P2860
P304
12882-12917
P356
10.1039/C3RA45702H
P577
2014-01-01T00:00:00Z