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The Cyclisation of l-Aryl-2-Benzamidoalkan-l-Ols to 4,5-DihydroOxazoles or Isoquinolines

The cyclisation of several N-benzoyl derivatives of 2-amino-l-phenylpropan-l-ol w~e carried out employing the Pictet-Cams modification ofthe BischlerNapieralski reaction. The formation of4, 5-dihydro-oxazoles orisoquinolines depends on the substituents on the N-benzoyl group. The mode of formation...

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Main Authors: Md. Sharif, Atan, O. Fitton, Alan
Format: Article
Language:English
English
Published: 1990
Online Access:http://psasir.upm.edu.my/id/eprint/2898/1/The_Cyclisation_of_l-Aryl-2-Benzamidoalkan-l-Ols_to_4%2C5-DihydroOxazoles.pdf
http://psasir.upm.edu.my/id/eprint/2898/
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spelling my.upm.eprints.28982013-05-27T07:04:15Z http://psasir.upm.edu.my/id/eprint/2898/ The Cyclisation of l-Aryl-2-Benzamidoalkan-l-Ols to 4,5-DihydroOxazoles or Isoquinolines Md. Sharif, Atan O. Fitton, Alan The cyclisation of several N-benzoyl derivatives of 2-amino-l-phenylpropan-l-ol w~e carried out employing the Pictet-Cams modification ofthe BischlerNapieralski reaction. The formation of4, 5-dihydro-oxazoles orisoquinolines depends on the substituents on the N-benzoyl group. The mode of formation of the products is discussed. 1990 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/2898/1/The_Cyclisation_of_l-Aryl-2-Benzamidoalkan-l-Ols_to_4%2C5-DihydroOxazoles.pdf Md. Sharif, Atan and O. Fitton, Alan (1990) The Cyclisation of l-Aryl-2-Benzamidoalkan-l-Ols to 4,5-DihydroOxazoles or Isoquinolines. Pertanika, 13 (3). pp. 389-393. English
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
English
description The cyclisation of several N-benzoyl derivatives of 2-amino-l-phenylpropan-l-ol w~e carried out employing the Pictet-Cams modification ofthe BischlerNapieralski reaction. The formation of4, 5-dihydro-oxazoles orisoquinolines depends on the substituents on the N-benzoyl group. The mode of formation of the products is discussed.
format Article
author Md. Sharif, Atan
O. Fitton, Alan
spellingShingle Md. Sharif, Atan
O. Fitton, Alan
The Cyclisation of l-Aryl-2-Benzamidoalkan-l-Ols to 4,5-DihydroOxazoles or Isoquinolines
author_facet Md. Sharif, Atan
O. Fitton, Alan
author_sort Md. Sharif, Atan
title The Cyclisation of l-Aryl-2-Benzamidoalkan-l-Ols to 4,5-DihydroOxazoles or Isoquinolines
title_short The Cyclisation of l-Aryl-2-Benzamidoalkan-l-Ols to 4,5-DihydroOxazoles or Isoquinolines
title_full The Cyclisation of l-Aryl-2-Benzamidoalkan-l-Ols to 4,5-DihydroOxazoles or Isoquinolines
title_fullStr The Cyclisation of l-Aryl-2-Benzamidoalkan-l-Ols to 4,5-DihydroOxazoles or Isoquinolines
title_full_unstemmed The Cyclisation of l-Aryl-2-Benzamidoalkan-l-Ols to 4,5-DihydroOxazoles or Isoquinolines
title_sort cyclisation of l-aryl-2-benzamidoalkan-l-ols to 4,5-dihydrooxazoles or isoquinolines
publishDate 1990
url http://psasir.upm.edu.my/id/eprint/2898/1/The_Cyclisation_of_l-Aryl-2-Benzamidoalkan-l-Ols_to_4%2C5-DihydroOxazoles.pdf
http://psasir.upm.edu.my/id/eprint/2898/
_version_ 1643822454100983808
score 13.214268

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