Articles with "secondary alcohols" as a keyword



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An Engineered Cholesterol Oxidase Catalyses Enantioselective Oxidation of Non‐steroidal Secondary Alcohols

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Published in 2022 at "ChemBioChem"

DOI: 10.1002/cbic.202200075

Abstract: The enantioselective oxidation of 2° alcohols to ketones is an important reaction in synthetic chemistry, especially if it can be achieved using O2‐driven alcohol oxidases under mild reaction conditions. However to date, oxidation of secondary… read more here.

Keywords: enantioselective oxidation; oxidation; cholesterol oxidase; secondary alcohols ... See more keywords
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CpNiBr(NHC) complexes as pre-catalysts in the chemoselective anaerobic oxidation of secondary aryl alcohols: Experimental and DFT studies

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Published in 2017 at "Molecular Catalysis"

DOI: 10.1016/j.mcat.2016.12.023

Abstract: Abstract Nine Ni(II)-NHC complexes of the type [CpNiBr(NHC)], each containing either a symmetric or asymmetric alkyl/benzyl/phenylethyl imidazolium ligand, effectively catalysed the anaerobic oxidation of a series of secondary alcohols, including 1-phenylethanol to yield acetophenone. Catalytic… read more here.

Keywords: secondary alcohols; nhc complexes; anaerobic oxidation; cpnibr nhc ... See more keywords
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Application of deuterated THENA for assigning the absolute configuration of chiral secondary alcohols

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Published in 2019 at "Tetrahedron Letters"

DOI: 10.1016/j.tetlet.2019.01.013

Abstract: Abstract The structure of a constrained bicyclic chiral derivatizing agent (CDA), 1,2,3,4-tetrahydro-1,4-epoxynaphthalene-1-carboxylic acid, THENA 1, was modified by replacing both exo-methylene protons with deuterium atoms. The modified CDA, THENA-d2 2, could be used to assign… read more here.

Keywords: secondary alcohols; absolute configuration; configuration chiral; chiral secondary ... See more keywords
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Switchable β-alkylation of Secondary Alcohols with Primary Alcohols by a Well-Defined Cobalt Catalyst

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Published in 2021 at "Organometallics"

DOI: 10.1021/acs.organomet.1c00147

Abstract: β-alkylation of secondary alcohols with primary alcohols to selectively generate alcohols by a well-defined Co catalyst is presented. Remarkably, a low catalyst loading of 0.7 mol % can be employed... read more here.

Keywords: secondary alcohols; primary alcohols; alcohols well; catalyst ... See more keywords
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Compartmentalized Nanoreactors for One-Pot Redox-Driven Transformations

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Published in 2019 at "ACS Catalysis"

DOI: 10.1021/acscatal.8b04667

Abstract: This contribution introduces poly(2-oxazoline)-based shell cross-linked micelles (SCMs) as nanoreactors to realize one-pot redox-driven deracemizations of secondary alcohols in aqueous media. TEMPO and Rh-TsDPEN moieties are spatially positioned into the hydrophilic corona and the hydrophobic… read more here.

Keywords: redox driven; secondary alcohols; one pot; pot redox ... See more keywords
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Hydrogen Borrowing Catalysis with Secondary Alcohols: A New Route for the Generation of β-Branched Carbonyl Compounds.

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Published in 2017 at "Journal of the American Chemical Society"

DOI: 10.1021/jacs.6b12840

Abstract: A hydrogen borrowing reaction employing secondary alcohols and Ph* (Me5C6) ketones to give β-branched carbonyl products is described (21 examples). This new C-C bond forming process requires low loadings of [Cp*IrCl2]2, relatively low temperatures, and… read more here.

Keywords: borrowing catalysis; hydrogen borrowing; alcohols new; catalysis secondary ... See more keywords
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Aldehyde/ketone-catalyzed highly selective synthesis of 9-monoalkylated fluorenes by dehydrative C-alkylation with primary and secondary alcohols

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Published in 2017 at "Green Chemistry"

DOI: 10.1039/c6gc02518h

Abstract: By using aldehydes or ketones as the catalyst and screening CsOH out as the more effective base than KOH in many instances, an efficient 9-C-alkylation of fluorenes with alcohols was achieved to provide a green… read more here.

Keywords: monoalkylated fluorenes; aldehyde ketone; primary secondary; secondary alcohols ... See more keywords
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Ni-Catalyzed dehydrogenative coupling of primary and secondary alcohols with methyl-N-heteroaromatics

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Published in 2018 at "Organic chemistry frontiers"

DOI: 10.1039/c8qo00764k

Abstract: Here we report the first base-metal catalyzed dehydrogenative coupling of primary (aromatic, heteroaromatic, and aliphatic) and secondary alcohols with methyl-N-heteroaromatics to form various C(sp3)-alkylated N-heteroaromatics. The reaction is enabled by Earth abundant, non-precious NiBr2 as… read more here.

Keywords: coupling primary; catalyzed dehydrogenative; methyl heteroaromatics; secondary alcohols ... See more keywords
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Ruthenium(ii)-catalysed direct synthesis of ketazines using secondary alcohols.

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Published in 2019 at "Chemical communications"

DOI: 10.1039/c9cc01383k

Abstract: Direct one-pot synthesis of ketazines from secondary alcohols and hydrazine hydrate catalyzed by a ruthenium pincer complex is reported, which proceeds through O-H bond activation of secondary alcohols via amine-amide metal-ligand cooperation in the catalyst.… read more here.

Keywords: direct synthesis; secondary alcohols; synthesis ketazines; catalysed direct ... See more keywords
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Catalytic deoxygenation of bio-based 3-hydroxydecanoic acid to secondary alcohols and alkanes

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Published in 2020 at "Green Chemistry"

DOI: 10.1039/d0gc00691b

Abstract: This work comprises the selective deoxygenation of bio-derivable 3-hydroxydecanoic acid to either linear alkanes or secondary alcohols in aqueous phase and H2-atmosphere over supported metal catalysts. Among the screened catalysts, Ru-based systems were identified to… read more here.

Keywords: deoxygenation bio; hydroxydecanoic acid; catalytic deoxygenation; secondary alcohols ... See more keywords
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Assignment of the Absolute Configuration of Secondary Alcohols by 13C NMR and its Correlation with Methyl-1-(chloromethyl)-oxopyrrolidine-2-carboxylate and Quantum-Mechanical GIAO Calculations

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Published in 2023 at "New Journal of Chemistry"

DOI: 10.1039/d2nj05887a

Abstract: Analysis of the effect of steric compression on the chemical shifts of carbons (13C NMR) in diastereoisomers is an accessible strategy for assigning the absolute configuration of secondary alcohols. Here... read more here.

Keywords: absolute configuration; secondary alcohols; assignment absolute; configuration secondary ... See more keywords