A novel, facile methodology for the synthesis of N,N′-bis(tert-butoxycarbonyl)-protected guanidines using polymer-supported carbodiimide
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Guisado, O
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Johnson & Johnson Pharmaceut Res & Dev, High Throughput Chem Grp, Ctr Invest Quim, Toledo 45007, SpainJohnson & Johnson Pharmaceut Res & Dev, High Throughput Chem Grp, Ctr Invest Quim, Toledo 45007, Spain
Guisado, O
[1
]
Martínez, S
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Johnson & Johnson Pharmaceut Res & Dev, High Throughput Chem Grp, Ctr Invest Quim, Toledo 45007, SpainJohnson & Johnson Pharmaceut Res & Dev, High Throughput Chem Grp, Ctr Invest Quim, Toledo 45007, Spain
Martínez, S
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]
Pastor, J
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Johnson & Johnson Pharmaceut Res & Dev, High Throughput Chem Grp, Ctr Invest Quim, Toledo 45007, SpainJohnson & Johnson Pharmaceut Res & Dev, High Throughput Chem Grp, Ctr Invest Quim, Toledo 45007, Spain
Pastor, J
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]
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[1] Johnson & Johnson Pharmaceut Res & Dev, High Throughput Chem Grp, Ctr Invest Quim, Toledo 45007, Spain
A novel methodology for the synthesis of guanidines front amines has been developed using polymer assisted synthesis, potentially allowing the preparation of series of compounds in a high throughput Manner. The methodology comprises the use of polymer-supported carbodiimide as the activating agent for N,N'-bis(tert-butoxycarbonyl) thiourea with polymer-supported trisamine as a scavenger, followed by deprotection with trifluoroacetic acid. For the first time, polymer-supported carbodiimide has been utilized as an activating agent to synthesize guanidines. (C) 2002 Elsevier Science Ltd. All rights reserved.