Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles

Angewandte Chemie ◽

10.1002/ange.202013062 ◽

2020 ◽

Author(s):

Hai Huang ◽

Tianyu Zhang ◽

Jianwei Sun

Keyword(s):

Ring Opening ◽

Bond Formation ◽

Carbon Nucleophiles ◽

Acid Catalyzed ◽

Soft Carbon ◽

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Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles

Angewandte Chemie International Edition ◽

10.1002/anie.202013062 ◽

2020 ◽

Author(s):

Hai Huang ◽

Tianyu Zhang ◽

Jianwei Sun

Keyword(s):

Ring Opening ◽

Bond Formation ◽

Carbon Nucleophiles ◽

Acid Catalyzed ◽

Soft Carbon ◽

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Synthesis of Medium-Sized Carbocycles via a Bidentate Lewis Acid-Catalyzed Inverse Electron-Demand Diels–Alder Reaction Followed by Photoinduced Ring-Opening

Organic Letters ◽

10.1021/acs.orglett.1c00249 ◽

2021 ◽

Author(s):

Julia Ruhl ◽

Sebastian Ahles ◽

Marcel A. Strauss ◽

Christopher M. Leonhardt ◽

Hermann A. Wegner

Keyword(s):

Ring Opening ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Acid Catalyzed ◽

Electron Demand

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Transition Metal-based Lewis Acid Catalyzed Ring Opening of Epoxides Using Amines Under Solvent-Free Conditions

Synlett ◽

10.1055/s-2004-822910 ◽

2004 ◽

pp. 1122-1122

Author(s):

Li-Wen Xu ◽

Chun-Gu Xia ◽

Pei-Qing Zhao

Keyword(s):

Transition Metal ◽

Ring Opening ◽

Solvent Free ◽

Solvent Free Conditions ◽

Ring Opening Of Epoxides ◽

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A Mild Procedure for the Lewis Acid-Catalyzed Ring-Opening of Activated Cyclopropanes with Amine Nucleophiles

Organic Letters ◽

10.1021/ol8009286 ◽

2008 ◽

Vol 10 (13) ◽

pp. 2809-2812 ◽

Author(s):

Olga Lifchits ◽

André B. Charette

Keyword(s):

Ring Opening ◽

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ChemInform Abstract: Lewis Acid Catalyzed Ring-Opening Reactions of Semicyclic N,O-Acetals Possessing an Exocyclic Nitrogen Atom: Mechanistic Aspect and Application to Piperidine Alkaloid Synthesis.

10.1002/chin.200221061 ◽

2010 ◽

Vol 33 (21) ◽

pp. no-no

Author(s):

Masaharu Sugiura ◽

Hiroyuki Hagio ◽

Ryoji Hirabayashi ◽

Shu Kobayashi

Keyword(s):

Nitrogen Atom ◽

Ring Opening ◽

Alkaloid Synthesis ◽

Ring Opening Reactions ◽

Acid Catalyzed ◽

Mechanistic Aspect ◽

Exocyclic Nitrogen Atom

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Synthesis of medium-sized cyclic γ-haloketones by radical mediated ring-opening reaction of Lewis acid catalyzed (2+2)-cycloaddition products

Tetrahedron Letters ◽

10.1016/j.tetlet.2004.12.024 ◽

2005 ◽

Vol 46 (6) ◽

pp. 1005-1008 ◽

Author(s):

Kiyosei Takasu ◽

Satoshi Nagao ◽

Masataka Ihara

Keyword(s):

Ring Opening ◽

Ring Opening Reaction ◽

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The Tsuji–Trost Reaction and Related Carbon–Carbon Bond Formation Reactions: Palladium-Catalyzed Reactions of Soft Carbon Nucleophiles with Dienes, Vinylcyclopropanes, and Related Compounds

Handbook of Organopalladium Chemistry for Organic Synthesis ◽

10.1002/0471212466.ch78 ◽

2005 ◽

pp. 1833-1844 ◽

Author(s):

Hiroyuki Nakamura ◽

Yoshinori Yamamoto

Keyword(s):

Bond Formation ◽

Carbon Bond ◽

Carbon Nucleophiles ◽

Carbon Carbon Bond ◽

Palladium Catalyzed ◽

Soft Carbon ◽

Catalyzed Reactions ◽

Related Compounds ◽

Bond Formation Reactions

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Lewis Acid Catalyzed Ring-Opening 1,3-Aminothiolation of Donor–Acceptor Cyclopropanes Using Sulfenamides

Organic Letters ◽

10.1021/acs.orglett.0c00483 ◽

2020 ◽

Vol 22 (6) ◽

pp. 2276-2280 ◽

Author(s):

Avishek Guin ◽

Thukaram Rathod ◽

Rahul N. Gaykar ◽

Tony Roy ◽

Akkattu T. Biju

Keyword(s):

Ring Opening ◽

Donor Acceptor ◽

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ChemInform Abstract: A NOVEL CARBON-CARBON BOND FORMATION BY THE LEWIS ACID CATALYZED REACTION OF β-STYRYLSILANE WITH ACETAL

Chemischer Informationsdienst ◽

10.1002/chin.198204155 ◽

1982 ◽

Vol 13 (4) ◽

Author(s):

T. HIRAO ◽

S. KOHNO ◽

J. ENDA ◽

Y. OHSHIRO ◽

T. AGAWA

Keyword(s):

Bond Formation ◽

Carbon Bond ◽

Carbon Carbon Bond ◽

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ChemInform Abstract: Lewis Acid-Catalyzed Ring-Opening Addition Reactions of Alcohols to Vinylcyclopropane.

10.1002/chin.201621043 ◽

2016 ◽

Vol 47 (21) ◽

Author(s):

Shin-ichi Matsuoka ◽

Kazuki Numata ◽

Masato Suzuki

Keyword(s):

Ring Opening ◽

Addition Reactions ◽

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