Synthesis of oxytocin analogues modified in the tripeptide side-chain by condensation of aminoterminal linear hexapeptide with the carboxyterminal tripeptide
1979 ◽
Vol 44
(1)
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pp. 275-287
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For the synthesis of oxytocin (Ia) analogues modified in the carboxyterminal part of the molecule, a method based on the condensation of protected aminoterminal hexapeptide with tripeptides by the action of dicyclohexylcarbodiimide and pentafluorophenol in the presence of 1-hydroxybenzotriazole was devised. Using this method [7-[U-13C]proline]oxytocin (Ib), des-9-glycine-oxytocin (Ic) and methyl ester of oxytocinoic acid ([9-glycine methyl ester]oxytocin) (Id) were prepared.
2009 ◽
Vol 24
(6)
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pp. 588-596
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2010 ◽
Vol 39
(5)
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pp. 639-653
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1995 ◽
Vol 51
(11)
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pp. 2362-2364
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Keyword(s):
2000 ◽
Vol 3
(3)
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pp. 381-387
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Keyword(s):
1974 ◽
Vol 52
(11)
◽
pp. 1018-1023
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Keyword(s):