Regioselectivity in intramolecular nucleophilic aromatic substitution. Synthesis of the potent anti HIV-I 8-halo TIBO analogs
KA Parker, CA Coburn
Index: Parker, Kathlyn A.; Coburn, Craig A. Journal of Organic Chemistry, 1992 , vol. 57, # 1 p. 97 - 100
Full Text: HTML
Citation Number: 36
Abstract
In a recent communication,'we described the synthesis of TIBO R82150 (la), an inhibitor of HIV-1 replication: by a four-step sequence. A key transformation in that four-step preparation was the conversion of intermediate 2a to bicyclic 3a by intramolecular nucleophilic aromatic substit~ tion.~
Related Articles:
[Ho; Kukla; Breslin; Ludovici; Grous; Diamond; Miranda; Rodgers; De Clercq; Pauwels; Andries; Janssen Journal of Medicinal Chemistry, 1995 , vol. 38, # 5 p. 794 - 802]
[Ho; Kukla; Breslin; Ludovici; Grous; Diamond; Miranda; Rodgers; De Clercq; Pauwels; Andries; Janssen Journal of Medicinal Chemistry, 1995 , vol. 38, # 5 p. 794 - 802]
[Ho; Kukla; Breslin; Ludovici; Grous; Diamond; Miranda; Rodgers; De Clercq; Pauwels; Andries; Janssen Journal of Medicinal Chemistry, 1995 , vol. 38, # 5 p. 794 - 802]
[Ho; Kukla; Breslin; Ludovici; Grous; Diamond; Miranda; Rodgers; De Clercq; Pauwels; Andries; Janssen Journal of Medicinal Chemistry, 1995 , vol. 38, # 5 p. 794 - 802]
[Ho; Kukla; Breslin; Ludovici; Grous; Diamond; Miranda; Rodgers; De Clercq; Pauwels; Andries; Janssen Journal of Medicinal Chemistry, 1995 , vol. 38, # 5 p. 794 - 802]