Abstract:A Conformationally Restrained Series of AT1-Selective Angiotensin II Antagonists.-The desired target compounds (VI) are restrained analogues of known AII receptor antagonists. The optimal products are the dihydroindanyl derivatives (a series). -(CARPINO, P. A.; SNEDDON, S. F.; DA SILVA JARDINE, P.; MAGNUS-AYRITEY, G. T.; RAUCH, A. L.; BURKARD, M. R.; Bioorg. Med. Chem. Lett. 4 (1994) 1, 93-98; Dep. Med.
“…Benzonitriles are converted into aryltetrazoles, hence the connection between 121 and 125 [138]. Higher substituted derivatives of the prototype compound 121 may be available by an in situ DoM silylation-ipso-halodesilylation method [28].…”
Section: Dom-cross-coupling Tactics Involving Ar-ar Bond Formationmentioning
“…Benzonitriles are converted into aryltetrazoles, hence the connection between 121 and 125 [138]. Higher substituted derivatives of the prototype compound 121 may be available by an in situ DoM silylation-ipso-halodesilylation method [28].…”
Section: Dom-cross-coupling Tactics Involving Ar-ar Bond Formationmentioning
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