a-Benzoyloxy- and a-methoxy-substituted glycine derivatives as atypical substrates for free-radical reactions with stannanes

Easton, Christopher; Peters, Steven C

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a-Benzoyloxy- and a-methoxy-substituted glycine derivatives as atypical substrates for free-radical reactions with stannanes

Date

1999

Authors

Easton, Christopher

Peters, Steven C

Publisher

Gordon and Breach

Abstract

α-Benzoyloxy-and α-methoxy-substituted glycine derivatives undergo homolytic reactions with tributyltin hydride to give the reduction product. With allyltributyltin they afford the product of allyl group transfer and the corresponding dimeric glycine de

Keywords

Keywords: Allyltributyltin; Benzoate; Free-radical; Hexabutylditin; Methoxide; Tributyltin hydride

URI

http://hdl.handle.net/1885/93777

Collections

ANU Research Publications

Source

Phosphorus, Sulfur, and Silicon and the Related Elements

Type

Journal article

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a-Benzoyloxy- and a-methoxy-substituted glycine derivatives as atypical substrates for free-radical reactions with stannanes

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