ChemInform Abstract: Detritylation with Ytterbium Triflate.

Rong Jian Lu; Daipei Liu; Roger W. Giese

doi:10.1002/chin.200031076

ChemInform Abstract: Detritylation with Ytterbium Triflate.

ChemInform ◽

10.1002/chin.200031076 ◽

2010 ◽

Vol 31 (31) ◽

pp. no-no

Author(s):

Rong Jian Lu ◽

Daipei Liu ◽

Roger W. Giese

Keyword(s):

Ytterbium Triflate

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Ytterbium Triflate: A Green Catalyst

Synlett ◽

10.1055/s-0029-1218515 ◽

2009 ◽

Vol 2010 (01) ◽

pp. 161-162

Author(s):

Carina Crucho

Keyword(s):

Green Catalyst ◽

Ytterbium Triflate

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ChemInform Abstract: Ytterbium Triflate Promoted Coupling of Phenols and Propiolic Acids: Synthesis of Coumarins.

ChemInform ◽

10.1002/chin.201643129 ◽

2016 ◽

Vol 47 (43) ◽

Author(s):

Serena Fiorito ◽

Francesco Epifano ◽

Vito A. Taddeo ◽

Salvatore Genovese

Keyword(s):

Ytterbium Triflate

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ChemInform Abstract: Ytterbium Triflate Catalyzed Ring Opening of Aziridines with Amines.

ChemInform ◽

10.1002/chin.199712095 ◽

2010 ◽

Vol 28 (12) ◽

pp. no-no

Author(s):

M. MEGURO ◽

Y. YAMAMOTO

Keyword(s):

Ring Opening ◽

Ytterbium Triflate

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Ytterbium Triflate Promoted Synthesis of Benzimidazole Derivatives.

ChemInform ◽

10.1002/chin.200451096 ◽

2004 ◽

Vol 35 (51) ◽

Author(s):

Massimo Curini ◽

Francesco Epifano ◽

Francesca Montanari ◽

Ornelio Rosati ◽

Sara Taccone

Keyword(s):

Benzimidazole Derivatives ◽

Ytterbium Triflate

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ChemInform Abstract: Ytterbium Triflate Catalyzed Meerwein-Ponndorf-Verley (MPV) Reduction.

ChemInform ◽

10.1002/chin.201222068 ◽

2012 ◽

Vol 43 (22) ◽

pp. no-no

Author(s):

Adriano Mollica ◽

Salvatore Genovese ◽

Francesco Pinnen ◽

Azzurra Stefanucci ◽

Massimo Curini ◽

...

Keyword(s):

Ytterbium Triflate ◽

Mpv Reduction

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ChemInform Abstract: Ytterbium Triflate-Assisted Catalytic Oxidative Cross-Coupling of 2-Naphthol Derivatives.

ChemInform ◽

10.1002/chin.200811091 ◽

2008 ◽

Vol 39 (11) ◽

Author(s):

Shigeki Habaue ◽

Tomohisa Temma ◽

Yukihiro Sugiyama ◽

Pei Yan

Keyword(s):

Cross Coupling ◽

Ytterbium Triflate ◽

Naphthol Derivatives

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Selective conversion of glucose into lactic acid with immobilized ytterbium triflate

Reaction Kinetics Mechanisms and Catalysis ◽

10.1007/s11144-018-1448-3 ◽

2018 ◽

Vol 125 (2) ◽

pp. 923-936 ◽

Cited By ~ 1

Author(s):

Wang Shiwei ◽

Wang Qibao

Keyword(s):

Lactic Acid ◽

Selective Conversion ◽

Ytterbium Triflate

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Ytterbium Triflate Catalyzed Reactions of Epoxide with Nitrogen Heterocycles Under Solvent-Free Condition

Synthetic Communications ◽

10.1081/scc-120022472 ◽

2003 ◽

Vol 33 (17) ◽

pp. 2989-2994 ◽

Cited By ~ 12

Author(s):

Sanzhong Luo ◽

Baolian Zhang ◽

Peng G. Wang ◽

Jin-Pei Cheng

Keyword(s):

Nitrogen Heterocycles ◽

Solvent Free ◽

Free Condition ◽

Solvent Free Condition ◽

Ytterbium Triflate ◽

Catalyzed Reactions

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Ytterbium Triflate Catalyzed Synthesis of Alkoxy-Substituted Donor−Acceptor Cyclobutanes and Their Formal [4 + 2] Cycloaddition with Imines: Stereoselective Synthesis of Piperidines

Organic Letters ◽

10.1021/ol102062t ◽

2010 ◽

Vol 12 (21) ◽

pp. 4732-4735 ◽

Cited By ~ 72

Author(s):

Mahmoud M. Abd Rabo Moustafa ◽

Brian L. Pagenkopf

Keyword(s):

Stereoselective Synthesis ◽

Ytterbium Triflate ◽

Donor Acceptor

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Cationic Polymerization ofp-Methoxystyrene in Water with Dodecylbenzenesulfonic Acid and Ytterbium Triflate: Evidence for an Inverse Emulsion Process

Macromolecules ◽

10.1021/ma035942d ◽

2004 ◽

Vol 37 (9) ◽

pp. 3214-3221 ◽

Cited By ~ 26

Author(s):

Séverine Cauvin ◽

François Ganachaud ◽

Virginie Touchard ◽

Patrick Hémery ◽

Frédéric Leising

Keyword(s):

Cationic Polymerization ◽

Dodecylbenzenesulfonic Acid ◽

Inverse Emulsion ◽

Ytterbium Triflate ◽

Emulsion Process

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