3-Methyl-4H-[1,2,4]-oxadiazol-5-one: A versatile synthon for protecting monosubstituted acetamidines

Tetrahedron

Volumn 60, Issue 48, 2004, Pages 10907-10914

  Moormann, Alan E ^a   Wang, Jane L ^a   Palmquist, Katherine E ^a   Promo, Michele A ^a   Snyder, Jeffery S ^a   Scholten, Jeffrey A ^a   Massa, Mark A ^a   Sikorski, James A ^a,b   Webber, R Keith ^a  

^a PFIZER INC   (United States)

^b AtheroGenics Inc   (United States)

Author keywords

3 Methyl 4H 1,2,4 oxadiazol 5 one; Protected amidine

Indexed keywords

3 METHYL 4H [1,2,4]OXADIAZOL 5 ONE; ACETAMIDINE DERIVATIVE; ACID; ALKYL GROUP; AMIDINE; BASE; HYDROXYL GROUP; KETONE DERIVATIVE; OXADIAZOLE DERIVATIVE; POTASSIUM SALT; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; HYDROGENATION; HYDROLYSIS; MASS SPECTROMETRY; MICHAEL ADDITION; MITSUNOBU REACTION; MOLECULAR STABILITY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 14344260557     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.09.030     Document Type: Article

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