Pd-catalysed regiospecific reductive ring opening of epoxides and glycidic esters

Article abstract of DOI:10.1080/00397919508011782

The regiospecific ring opening of epoxides was achieved by Pd-catalysed transfer hydrogenolysis using ammonium formate as hydrogen source.

Full text of DOI:10.1080/00397919508011782

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Pd-Catalysed Regiospecific
Reductive Ring Opening of
Epoxides and Glycidic Esters
Jos P. Varghese a , Arumugam Sudalai a & Suresh Iyer
a
a National Chemical Laboratory , Pune, 411-008,
INDIA
Published online: 23 Sep 2006.
To cite this article: Jos P. Varghese , Arumugam Sudalai & Suresh Iyer (1995) Pd-
Catalysed Regiospecific Reductive Ring Opening of Epoxides and Glycidic Esters,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 25:15, 2267-2273, DOI: 10.1080/00397919508011782
To link to this article: http://dx.doi.org/10.1080/00397919508011782
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