4-N-aryl(benzyl)amino-4-hetaryl-1-butenes as building blocks in heterocyclic synthesis. 1. New route to 4,6-dimethyl-2-pyridylquinolines from the 4-N-p-methylphenylamino-4-pyridyl-1-butenes

DOI: 10.1515/HC.2001.7.4.323

Source and publish data:

Heterocyclic Communications p. 323 - 326 (2001)

Update date:2022-07-30

Topics:

Authors:

Vargas Mendez, Leonor Y.

Kouznetsov, Vladimir

Stashenko, Elena

Bahsas, Al

Amaro-Luis, Juan

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Article abstract of DOI:10.1515/HC.2001.7.4.323

Mediated-acid intramolecular cyclisation of 4-N-p-methylphenylamino-4-pyridyl-1-butenes 4-6 was used to obtain new C-2 pyridyl substituted 4,6-dimethyl-1,2,3,4-tetrahydroquinolines 7-9, which were oxidised then to their aromatic analogues 10-12 in good yi

Full text of DOI:10.1515/HC.2001.7.4.323

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Brought to you by | University of Sussex (University of Sussex)

Authenticated | 172.16.1.226

Download Date | 6/24/12 10:24 PM

Brought to you by | University of Sussex (University of Sussex)

Authenticated | 172.16.1.226

Download Date | 6/24/12 10:24 PM

Brought to you by | University of Sussex (University of Sussex)

Authenticated | 172.16.1.226

Download Date | 6/24/12 10:24 PM

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Article Doi

4-N-aryl(benzyl)amino-4-hetaryl-1-butenes as building blocks in heterocyclic synthesis. 1. New route to 4,6-dimethyl-2-pyridylquinolines from the 4-N-p-methylphenylamino-4-pyridyl-1-butenes

DOI: 10.1515/HC.2001.7.4.323

Source and publish data:

Authors:

Article abstract of DOI:10.1515/HC.2001.7.4.323

Full text of DOI:10.1515/HC.2001.7.4.323

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