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Miscellaneous Reactions Involving Silver Carbenoids

Mechanistically, most alkyne cyclizations of this type have been interpreted in terms of the catalyst serving as a Lewis acid, activating the n bond to nucleophilic attack,53-57 and while this pathway is feasible, the authors preferred one involving the intermediacy of a silver carbene.52 Control studies ruled out a pathway involving [Pg.253]

Our own endeavors in this area have been possible because of the hard work and valuable intellectual contributions of a number of coworkers, whose names appear in the references. Financial support has generously been provided by The Robert A. Welch Foundation (Y-1362). [Pg.255]

Issue number 8 of Chemical Reviews (Chem. Rev. 2008,108) was devoted to the utility of coinage metals in synthesis. [Pg.255]

We use the term carbene transfer to represent the net chemical transformation and not necessarily to imply that this is a reactive intermediate (either a free carbene or a metallo-carbene). [Pg.255]

Migita, T. Ando, W. Kondo, S. Matsuyama, H. Kosugi, M., Nippon Kagaku Zasshi 1970, 91, 374-377. [Pg.256]


See other pages where Miscellaneous Reactions Involving Silver Carbenoids is mentioned: [Pg.229]    [Pg.253]    [Pg.253]    [Pg.531]    [Pg.229]    [Pg.253]    [Pg.253]    [Pg.531]   


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Carbenoid

Carbenoid reactions

Carbenoids

Miscellaneous reactions

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