Solvent free one pot syntheses of highly substituted propargyl ethers and propargyl amines from propargyl alcohols catalyzed by recyclable alumina-sulfuric acid

[1]  S. Biswas,et al.  An Eco-friendly, One pot Synthesis of Tri-substituted Imidazoles in Aqueous Medium Catalyzed by RGO Supported Au Nano-catalyst and Computational Studies , 2021 .

[2]  A. Das,et al.  Chemoselective and ligand‐free aerobic oxidation of benzylic alcohols to carbonyl compounds using alumina‐supported mesoporous nickel nanoparticle as an efficient recyclable heterogeneous catalyst , 2021 .

[3]  A. Pramanik,et al.  Hydroarylation of alkynes and alkenes through alumina-sulfuric acid catalyzed regioselective C C bond formation , 2019, Tetrahedron Letters.

[4]  E. Bauer,et al.  Ruthenium complexes of the general formula [RuCl2(PHOX)2] as precatalysts in propargylic substitution reactions , 2018 .

[5]  S. Bhar,et al.  Catalysis by β‐Cyclodextrin Hydrate – Synthesis of 2,2‐Disubstituted 2H‐Chromenes in Aqueous Medium , 2016 .

[6]  U. Jana,et al.  Synthesis of Fused Dibenzofuran Derivatives via Palladium-Catalyzed Domino C-C Bond Formation and Iron-Catalyzed Cycloisomerization/Aromatization. , 2016, The Journal of organic chemistry.

[7]  S. Bhar,et al.  Chemoselective and ligand-free synthesis of diaryl ethers in aqueous medium using recyclable alumina-supported nickel nanoparticles , 2014 .

[8]  A. Pramanik,et al.  Eco-friendly synthesis of 2-aryl-1-arylmethyl-1H-benzimidazoles using alumina-sulfuric acid as a heterogeneous reusable catalyst , 2014 .

[9]  A. Pramanik,et al.  Alumina-sulfuric acid catalyzed eco-friendly synthesis of xanthenediones , 2012 .

[10]  Mukut Gohain,et al.  Al(OTf)3: an efficient recyclable catalyst for direct nucleophilic substitution of the hydroxy group of propargylic alcohols with carbon- and heteroatom-centered nucleophiles to construct C–C, C–O, C–N and C–S bonds , 2012 .

[11]  Etsuko Tokunaga,et al.  A New Synthetic Approach to Efavirenz through Enantioselective Trifluoromethylation by Using the Ruppert–Prakash Reagent , 2011 .

[12]  P. Lu,et al.  Tandem reaction of propargyl alcohol and N-sulfonylhydrazone: synthesis of dihydropyrazole and its utility in the preparation of 3,3-diarylacrylonitrile. , 2011, Organic letters.

[13]  P. Cozzi,et al.  Direct Nucleophilic SN1‐Type Reactions of Alcohols , 2011 .

[14]  Xiaodong Shi,et al.  Iron-catalyzed C-O bond activation for the synthesis of propargyl-1,2,3-triazoles and 1,1-bis-triazoles. , 2010, Organic letters.

[15]  M. Bao,et al.  New Application of N-Halosuccinimide/PPh3 for the Halogenation of Propargyl Alcohols to Haloallenes , 2009 .

[16]  J. M. Clancy,et al.  Prodrugs for Amines , 2008, Molecules.

[17]  J. Yadav,et al.  Iodine-catalyzed C- and O-nucleophilic substitution reactions of aryl-propargyl methanols , 2007 .

[18]  Tohru Yamada,et al.  Carbon Dioxide-Mediated Catalytic Rearrangement of Propargyl Alcohols into α,β-Unsaturated Ketones , 2007 .

[19]  U. Jana,et al.  An FeCl3-catalyzed highly C3-selective Friedel–Crafts alkylation of indoles with alcohols , 2007 .

[20]  J. Yadav,et al.  Sc(OTf)3-catalyzed alkylation of indoles with propargyl alcohols: an expeditious synthesis of 3-substituted indoles , 2007 .

[21]  H. Mayr,et al.  Electrophilic allylations and benzylations of indoles in neutral aqueous or alcoholic solutions. , 2006, Organic letters.

[22]  G. Dudley,et al.  Olefination of ketones using a gold(III)-catalyzed Meyer-Schuster rearrangement. , 2006, Organic letters.

[23]  Zhuang-Ping Zhan,et al.  BiCl3-catalyzed propargylic substitution reaction of propargylic alcohols with C-, O-, S- and N-centered nucleophiles. , 2006, Chemical communications.

[24]  Xichen Lin,et al.  Explorations on the total synthesis of the unusual marine alkaloid chartelline A. , 2006, The Journal of organic chemistry.

[25]  J. Campagne,et al.  Gold(III)-catalyzed nucleophilic substitution of propargylic alcohols. , 2005, Journal of the American Chemical Society.

[26]  Arijit Das,et al.  Selective reductive cleavage of 2,3-epoxybromides by the InCl3–NaBH4 reagent system , 2004 .

[27]  F. Toste,et al.  Rhenium-catalyzed aromatic propargylation. , 2004, Organic letters.

[28]  M. Bandini,et al.  New catalytic approaches in the stereoselective Friedel-Crafts alkylation reaction. , 2004, Angewandte Chemie.

[29]  彭志华,et al.  Palladium-Catalyzed Functionalization of Indoles with 2-Acetoxymethyl-Substituted Electron-Deficient Alkenes , 2004 .

[30]  M. Youdim,et al.  The importance of propargylamine moiety in the anti‐ Parkinson drug rasagiline and its derivatives for MAPK‐ dependent amyloid precursor protein processing , 2003, The FASEB Journal.

[31]  B. Trost,et al.  On inventing reactions for atom economy. , 2002, Accounts of chemical research.

[32]  D. MacMillan,et al.  Enantioselective organocatalytic indole alkylations. Design of a new and highly effective chiral amine for iminium catalysis. , 2002, Journal of the American Chemical Society.

[33]  S. G. Nelson,et al.  Ligand-Modified Catalysts for the McMurry Pinacol Reaction , 1997 .

[34]  B. M. Trost Atomökonomische Synthesen – eine Herausforderung in der Organischen Chemie: die Homogenkatalyse als wegweisende Methode , 1995 .

[35]  D. Egan,et al.  Design of a well-absorbed renin inhibitor. , 1991, Journal of medicinal chemistry.

[36]  K. Gates,et al.  5-(Aminomethyl)-3-aryl-2-oxazolidinones. A novel class of mechanism-based inactivators of monoamine oxidase B , 1990 .

[37]  K. Furuta,et al.  Regio- and Stereocontrolled Synthesis of Allenic and Acetylenic Derivatives. Organotitanium and Boron Reagents , 1984 .