Hydroboration of 1-allyl-1, 2, 3, 4-tetrahydroquinoline
S Kafka, M Ferles, M Richter
Index: Kafka, Stanislav; Ferles, Miloslav; Richter, Miloslav Collection of Czechoslovak Chemical Communications, 1985 , vol. 50, # 5 p. 1194 - 1200
Full Text: HTML
Citation Number: 1
Abstract
Abstract Hydroboration of 1-allyl-1, 2, 3, 4-tetrahydroquinoline (I) with triethylamine-borane in the molar ratio 1: 1 afforded a product from which 6, 7-benzo-5-aza-1-boraspiro [4, 5] decane (II) was isolated. Ethanolysis of II gave diethyl 3-(1, 2, 3, 4-tetrahydro-1-quinolyl) propylboronate (III). Acid hydrolysis of the crude hydroboration product and subsequent oxidation with alkaline hydrogen peroxide led to a mixture of 3-(1, 2, 3, 4-tetrahydro-1- ...
Related Articles:
A facile one-pot synthesis of N-substituted tetrahydroquinolines
[Babu, Thelagathoti Hari; Shanthi, Gnanamani; Perumal, Paramasivan T. Tetrahedron Letters, 2009 , vol. 50, # 24 p. 2881 - 2884]