Literature DB >> 12785827

Efficient and rapid C-Si bond cleavage in supercritical water.

Kenichiro Itami1, Koji Terakawa, Jun-Ichi Yoshida, Okitsugu Kajimoto.   

Abstract

Arylsilanes, alkenylsilanes, allylic silanes, and alkylsilanes were found to undergo extremely facile and rapid C-Si bond cleavage in supercritical water. The rapid C-Si bond cleavage occurred even with robust unactivated tetraalkylsilanes. The control experiments revealed the dramatic difference between supercritical and subcritical conditions and that between supercritical water and supercritical methanol, attesting to a unique reactivity of supercritical water in C-Si bond cleavage.

Entities:  

Year:  2003        PMID: 12785827     DOI: 10.1021/ja034227g

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  4 in total

1.  Silicon-Carbon Bond Formation via Nickel-Catalyzed Cross-Coupling of Silicon Nucleophiles with Unactivated Secondary and Tertiary Alkyl Electrophiles.

Authors:  Crystal K Chu; Yufan Liang; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2016-05-17       Impact factor: 15.419

2.  Practical multigram-scale synthesis of 4,6- and 4,8-sphingadienes, chemopreventive sphingoid bases.

Authors:  Hoe-Sup Byun; Robert Bittman
Journal:  Chem Phys Lipids       Date:  2012-10-17       Impact factor: 3.329

3.  Palladium-Catalyzed Cross-Coupling of Monochlorosilanes And Grignard Reagents.

Authors:  Bojan Vulovic; Andrew P Cinderella; Donald A Watson
Journal:  ACS Catal       Date:  2017-10-30       Impact factor: 13.084

4.  Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction.

Authors:  Andrew P Cinderella; Bojan Vulovic; Donald A Watson
Journal:  J Am Chem Soc       Date:  2017-06-01       Impact factor: 15.419

  4 in total

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