The Birch reduction of heterocyclic compounds. IV. Birch reduction of 3- acylfurans. Competition between ring reduction, carbonyl Reduction, and dimer formation

DOI: 10.1002/jhet.5570350608

Source and publish data:

Journal of Heterocyclic Chemistry p. 1285 - 1293 (1998)

Update date:2022-08-05

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Authors:

Takano, Daisuke

Nakajima, Yoshitaka

Miyahara, Ikuko

Hirotsu, Ken

Tanaka, Rika

Okada, Keiji

Morimoto, Yoshiki

Kinoshita, Takamasa

Yoshihara, Kazuo

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Article abstract of DOI:10.1002/jhet.5570350608

The Birch reduction of 3-acylfurans 1, 3 and 10 and their reaction path ways are described.

Full text of DOI:10.1002/jhet.5570350608

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Article Doi

The Birch reduction of heterocyclic compounds. IV. Birch reduction of 3- acylfurans. Competition between ring reduction, carbonyl Reduction, and dimer formation

DOI: 10.1002/jhet.5570350608

Source and publish data:

Authors:

Article abstract of DOI:10.1002/jhet.5570350608

Full text of DOI:10.1002/jhet.5570350608

Products guided by the article

R&D Labs maybe for 160805-71-0

Relevant to this article

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