Anhydrous zirconium(IV) sulfate and tin(IV) sulfate: solid Lewis acid catalysts in liquid-phase hydro-acyloxy-addition reactions?

Ivo J. Dijs; Roene de Koning; John W. Geus; Leonardus W. Jenneskens

doi:10.1039/b105049b

Anhydrous zirconium(IV) sulfate and tin(IV) sulfate: solid Lewis acid catalysts in liquid-phase hydro-acyloxy-addition reactions?

Physical Chemistry Chemical Physics ◽

10.1039/b105049b ◽

2001 ◽

Vol 3 (19) ◽

pp. 4423-4429 ◽

Cited By ~ 7

Author(s):

Ivo J. Dijs ◽

Roene de Koning ◽

John W. Geus ◽

Leonardus W. Jenneskens

Keyword(s):

Liquid Phase ◽

Lewis Acid ◽

Addition Reactions ◽

Acid Catalysts ◽

Lewis Acid Catalysts

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Carbocations as Lewis Acid Catalysts in Diels-Alder and Michael Addition Reactions

Chemistry - A European Journal ◽

10.1002/chem.201304160 ◽

2013 ◽

Vol 20 (4) ◽

pp. 1066-1072 ◽

Cited By ~ 51

Author(s):

Juho Bah ◽

Johan Franzén

Keyword(s):

Lewis Acid ◽

Michael Addition ◽

Diels Alder ◽

Addition Reactions ◽

Acid Catalysts ◽

Lewis Acid Catalysts

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ChemInform Abstract: Carbocations as Lewis Acid Catalysts in Diels-Alder and Michael Addition Reactions.

ChemInform ◽

10.1002/chin.201427035 ◽

2014 ◽

Vol 45 (27) ◽

pp. no-no

Author(s):

Juho Bah ◽

Johan Franzen

Keyword(s):

Lewis Acid ◽

Michael Addition ◽

Diels Alder ◽

Addition Reactions ◽

Acid Catalysts ◽

Lewis Acid Catalysts

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Hydrothermal synthesis of Sn-Beta zeolites in F−-free medium

Inorganic Chemistry Frontiers ◽

10.1039/c8qi00672e ◽

2018 ◽

Vol 5 (11) ◽

pp. 2763-2771 ◽

Cited By ~ 5

Author(s):

Hao Xu ◽

Xudong Wang ◽

Peng Ji ◽

Haihong Wu ◽

Yejun Guan ◽

...

Keyword(s):

Hydrothermal Synthesis ◽

Lewis Acid ◽

Crystal Size ◽

Acid Catalysts ◽

Free Medium ◽

Lewis Acid Catalysts ◽

Structure Directing Agent ◽

Highly Active ◽

Beta Zeolites

Sn-Beta zeolites, with high Sn content and smaller crystal size, hydrothermally synthesized in F−-free medium using N-cyclohexyl-N,N-dimethylcyclohexanaminium hydroxide as the structure-directing agent with the assistance of Na+ and seed, are highly active as Lewis acid catalysts.

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Metal-Dependent Reactivity of Electrophilic Platinum Group Metal Lewis Acid Catalysts: Competitive Alkene Dimerization, Intramolecular Friedel−Crafts Alkylation, and Carbonyl-Ene Reactivity

Organometallics ◽

10.1021/om7006612 ◽

2007 ◽

Vol 26 (24) ◽

pp. 5961-5966 ◽

Cited By ~ 17

Author(s):

Simon Doherty ◽

Julian G. Knight ◽

Catherine H. Smyth ◽

Ross W. Harrington ◽

William Clegg

Keyword(s):

Lewis Acid ◽

Platinum Group Metal ◽

Acid Catalysts ◽

Lewis Acid Catalysts ◽

Group Metal ◽

Platinum Group

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Stereo- and Regio-Control of 1, 3-Dipolar Cycloaddition Reactions by the Aid of Lewis Acid Catalysts—Nitrone and aci-Nitro Compound Cycloadditions—

NIPPON KAGAKU KAISHI ◽

10.1246/nikkashi.2000.155 ◽

2000 ◽

Vol 2000 (3) ◽

pp. 155-165 ◽

Cited By ~ 1

Author(s):

Shuji KANEMASA

Keyword(s):

Lewis Acid ◽

Nitro Compound ◽

Dipolar Cycloaddition ◽

Acid Catalysts ◽

Cycloaddition Reactions ◽

Lewis Acid Catalysts

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A structural, DFT and experimental investigation of the ring stability and ring-opening polymerization behaviour of cyclic thionylphosphazenes in the presence of lewis acid catalysts

Polymer ◽

10.1016/j.polymer.2021.124196 ◽

2021 ◽

pp. 124196

Author(s):

Rachele N. Carafa ◽

Kristy V. Halnan ◽

R. Stephen Wylie ◽

Daniel A. Foucher ◽

Alan J. Lough ◽

...

Keyword(s):

Experimental Investigation ◽

Lewis Acid ◽

Ring Opening ◽

Ring Opening Polymerization ◽

Acid Catalysts ◽

Lewis Acid Catalysts ◽

Ring Stability

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Application of arylboron difluoride Lewis acid catalysts to the Diels-Alder reaction: Convenient, non-volatile alternatives to boron trifluoride

Tetrahedron ◽

10.1016/s0040-4020(99)00472-x ◽

1999 ◽

Vol 55 (28) ◽

pp. 8547-8554 ◽

Cited By ~ 6

Author(s):

Maria Fé de la Torre ◽

M.Cruz Caballero ◽

Andrew Whiting

Keyword(s):

Lewis Acid ◽

Boron Trifluoride ◽

Alder Reaction ◽

Diels Alder ◽

Acid Catalysts ◽

Lewis Acid Catalysts ◽

Diels Alder Reaction

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Assessment of fluoroalkyltin compounds as fluorous Lewis acid catalysts

Applied Organometallic Chemistry ◽

10.1002/aoc.517 ◽

2003 ◽

Vol 17 (10) ◽

pp. 795-799 ◽

Cited By ~ 5

Author(s):

Yasuo Imakura ◽

Satoru Nishiguchi ◽

Akihiro Orita ◽

Junzo Otera

Keyword(s):

Lewis Acid ◽

Acid Catalysts ◽

Lewis Acid Catalysts

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ChemInform Abstract: Calcium-Based Lewis Acid Catalysts

ChemInform ◽

10.1002/chin.201340223 ◽

2013 ◽

Vol 44 (40) ◽

pp. no-no

Author(s):

Jeanne-Marie Begouin ◽

Meike Niggemann

Keyword(s):

Lewis Acid ◽

Acid Catalysts ◽

Lewis Acid Catalysts

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Catalyzed Orientation Reversals in Diels–Alder Reactions

Canadian Journal of Chemistry ◽

10.1139/v75-086 ◽

1975 ◽

Vol 53 (4) ◽

pp. 616-618 ◽

Cited By ~ 35

Author(s):

Žarko Stojanac ◽

Robert A. Dickinson ◽

Nada Stojanac ◽

Ronald J. Woznow ◽

Zdenek Valenta

Keyword(s):

Lewis Acid ◽

Diels Alder ◽

Acid Catalysts ◽

Acid Salt ◽

Lewis Acid Catalysts ◽

Preferential Formation ◽

Orientation Reversal

Lewis acid catalysts cause an orientation reversal in the Diels–Alder additions of 2,6-di-methyl-1,4-quinone (1) and toluquinone (12) to 1-substituted 1,3-butadienes and to 1,2- and 1,3-dialkyl dienes. These results are explained by the preferential formation of one reactive quinone–Lewis acid salt.

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