Frustrated Lewis pairs-assisted reduction of carbonyl compounds (original) (raw)
A novel reduction reaction for the conversion of aldehydes, ketones and primary, secondary and tertiary alcohols into their corresponding alkanes
Christopher McRae
Tetrahedron letters, 2006
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NaBH4/DOWEX(R)50WX4: A Convenient Reducing System for Fast and Efficient Reduction of Carbonyl Compounds to Their Corresponding Alcohols
awat alipouramjad
Journal of the Chinese Chemical Society, 2013
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NaBH4/(NH4)2SO4: A Convenient System for Reduction of Carbonyl Compounds to their Corresponding Alcohols in wet-THF
Davood Setamdideh
Oriental Journal of Chemistry, 2014
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Al(OiPr)3 as an Effective Catalyst for the Enhancement of Meerwein−Ponndorf−Verley (MPV) Reductions of Morita-Baylis-Hillman (MBH) cyclic alcohols
haitham elleuch
Journal of molecular structure, 2024
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ChemInform Abstract: REDUCTION OR ALKYLATIVE REDUCTION OF THE CARBONYL GROUP
Mireille Sevrin
Chemischer Informationsdienst, 1976
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Lanthanoids in organic syntheses 7. selective reductions of carbonyl groups in aqueous ethanol solution
Andre Gemal
Tetrahedron Letters, 1981
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A GENERAL METHOD FOR THE SELECTIVE REDUCTION OF KETONES IN THE PRESENCE OF ENONES
Sebastian Gallegos
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Lewis Acid-Catalyzed Oxidative Allylation: A New Approach for the Synthesis of Homoallylic Alcohols and Amines Directly from Alcohols
VISHNU P SRIVASTAVA
Advanced Synthesis & Catalysis, 2011
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Efficient One-Pot Reductive Aminations of Carbonyl Compounds with Aquivion-Fe as a Recyclable Catalyst and Sodium Borohydride
Stefano Paganelli
European Journal of Organic Chemistry, 2019
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Carbonyl Reduction of Functionalized Aldehydes and Ketones by Tri-n-Butyltin Hydride and SiO2
Xavier Franck
The Journal of Organic Chemistry, 1994
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Regioselective Catalytic Dehydrogenation of Aldehydes and Ketones
Anan Arisha
The Journal of Organic Chemistry, 1998
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Synthesis of Aldehydes by Rosenmund Reduction
vasanti yadav
Organic Process Research & Development, 1997
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Lithium n-butylborohydride as a selective reducing agent for the reduction of enones, cyclic ketones, and selected carbonyl compounds
Young-choon Moon
The Journal of Organic Chemistry, 1982
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Screening method for the evaluation of asymmetric catalysts for the reduction of aliphatic ketones
saoussen ZEROR
Tetrahedron Letters, 2011
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Direct reductive amination and selective 1,2-reduction of α,β-unsaturated aldehydes and ketones by NaBH4 using H3PW12O40 as catalyst
Mahmood Tajbakhsh
Tetrahedron Letters, 2007
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Expanding the Boundaries of Water-Tolerant Frustrated Lewis Pair Hydrogenation: Enhanced Back Strain in the Lewis Acid Enables the Reductive Amination of Carbonyls
Márk Szabó
Angewandte Chemie (International ed. in English), 2017
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Titanocene-catalysed, selective reduction of ketones in aqueous media. A safe, mild, inexpensive procedure for the synthesis of secondary alcohols via radical chemistry
Antonio Rosales
Tetrahedron Letters, 2003
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ChemInform Abstract: An Efficient and Heterogeneous Recyclable Palladium Catalyst for Chemoselective Conjugate Reduction of α,β-Unsaturated Carbonyls in Aqueous Medium
Ziyauddin Qureshi
ChemInform, 2011
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Direct reductive amination and selective 1, 2-reduction of-unsaturated aldehydes and ketones by NaBH4 using H3PW12O40 as catalyst
Jafar Akbari
Tetrahedron …, 2007
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An efficient and heterogeneous recyclable palladium catalyst for chemoselective conjugate reduction of α,β-unsaturated carbonyls in aqueous medium
Ziyauddin Qureshi
Green Chemistry, 2011
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A Simple Method for the Reduction of Carboxylic Acids to Aldehydes or Alcohols Using H 2 and Pd/C
Andrea Porcheddu
Journal of Organic Chemistry, 1999
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Laboratory evolution of an alcohol dehydrogenase towards enantioselective reduction of difficult-to-reduce ketones
Thao Chu
Bioresources and Bioprocessing, 2019
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An expedient route for the reduction of carboxylic acids to alcohols employing 1-propanephosphonic acid cyclic anhydride as acid activator
Nagendra G
Tetrahedron Letters, 2012
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Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles
Zheng-Wang Qu
Angewandte Chemie (International ed. in English), 2016
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A new catalytic enantioselective reducing reagent system from (−)-α,α-diphenylpyrrolidinemethanol and 9-borabicyclo[3.3.1]nonane, especially effective for hindered and substituted aralkylketones
Kanth Josyula
Tetrahedron, 2002
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Highly diastereoselective reduction of α-alkyl-β-hydroxy ketones with sodium and lithium boron hydrides via their titanium alcoholates
Marcella Bosco
Tetrahedron Letters, 1999
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Highly atom-efficient and chemoselective reduction of ketones in the presence of aldehydes using heterogeneous catalysts
Tomoo Mizugaki
Green Chemistry, 2013
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Development of silica-supported frustrated Lewis pairs: highly active transition metal-free catalysts for the Z-selective reduction of alkynes
Cyril Godard
Catalysis Science & Technology, 2016
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Regioselective and Chemoselective Reduction of ,-Unsaturated Carbonyl Compounds by /Ba as a Reducing System
Davood Setamdideh
Organic Chemistry International, 2013
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Roles of the Lewis Acid and Base in the Chemical Reduction of CO 2 Catalyzed by Frustrated Lewis Pairs
Aaron Holder, Chern-Hooi Lim
Inorganic Chemistry, 2013
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Efficient and Convenient Reduction of Organic Carbonyl Compounds to their Corresponding Alcohols by Zn(BH4)2/Charcoal in THF
Davood Setamdideh
Journal of the Mexican Chemical Society, 2012
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Selective Aldehyde Reduction in Ketoaldehydes with NaBH4-Na2CO3-H2O at Room Temperatures
Sosale Chandrasekhar
Synthetic Communications, 2014
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Oxazaborolidine-catalysed reduction of alk-2-ene-1,4-diones. A convenient access to chiral 1,4-diols
Jordi Garcia
Tetrahedron, 1998
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Highly Enantioenriched Propargylic Alcohols by Oxazaborolidine-Mediated Reduction of Acetylenic Ketones
Jordi Garcia
The Journal of Organic Chemistry, 1996
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Benzylation via Tandem Grignard Reaction - Iodotrimethylsilane (TMSI) Mediated Reduction
Reda Benhocine
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