Towards benign syntheses of bipyridines: Versatile approach to supramolecular building blocks

Gareth W.V. Cave; Colin L. Raston

doi:10.1016/j.tetlet.2005.02.081

Towards benign syntheses of bipyridines: Versatile approach to supramolecular building blocks

Gareth W.V. Cave, Colin L. Raston

Research output: Contribution to journal › Article › peer-review

16 Citations (Scopus)

Abstract

Chiral and achiral bipyridines are readily accessible via a solvent-free Michael addition involving solid NaOH, followed by treatment with ammonium acetate in acetic acid, as a 'one pot' more benign protocol, affording pure products in high yield, typically >80%.

Original language	English
Pages (from-to)	2361-2363
Number of pages	3
Journal	Tetrahedron Letters
Volume	46
Issue number	14
DOIs	https://doi.org/10.1016/j.tetlet.2005.02.081
Publication status	Published - 4 Apr 2005
Externally published	Yes

Keywords

Green chemistry
Ketones
Pyridines
Solvent free

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10.1016/j.tetlet.2005.02.081Licence: In Copyright

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abstract = "Chiral and achiral bipyridines are readily accessible via a solvent-free Michael addition involving solid NaOH, followed by treatment with ammonium acetate in acetic acid, as a 'one pot' more benign protocol, affording pure products in high yield, typically >80%.",

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AU - Raston, Colin L.

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KW - Green chemistry

KW - Ketones

KW - Pyridines

KW - Solvent free

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JO - Tetrahedron Letters

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IS - 14

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Towards benign syntheses of bipyridines: Versatile approach to supramolecular building blocks

Abstract

Keywords

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