TRANSFORMATIONS OF 4-N-ARYLAMINO-4-(8-QUINOLINYL)-I-BUTENES AND 3-ARYL-2-(8-QUINOLINYL)-4-THIAZOLIDINONES
✍ Scribed by Mendez, Leonor Y. Vargas; Kouznetsov, Vladimir; Poveda, Juan C.; Yolaçan, Cigdem; Öcal, Nüket; Aydogan, Feray
- Book ID
- 120668400
- Publisher
- Walter de Gruyter GmbH & Co. KG
- Year
- 2001
- Tongue
- English
- Weight
- 993 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0793-0283
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## Abstract The enantiomers of [3‐^3^H]‐2‐[[4‐[(7‐chloro‐4‐quinolinyl)amino]pentyl]ethylamino]ethanol,[3‐^3^H]‐hydroxychloroquine, (R)‐8 and (S)‐8, have been prepared in two steps from the known precursors 4,7‐dichloro‐3‐iodoquinoline, 4, and the enantiomers of 2‐[(4‐aminopentyl)ethylamino]ethanol,
Microwave Assisted Synthesis of Phenyl(2-phenyl-5,6,7,8-tetrahydro--4-quinolinyl)methanone and Its Derivatives. -The hitherto unreported title compounds (IV) are obtained from triketones (III) via an one-pot oxidative amination--cyclization-aromatization protocol. The reaction rate is promoted by mi