aminoalcohol

O=C1COC2(CCN(C(=O)OCc3ccccc3)CC2)C(Cc2ccc(F)cc2)N1
Reaction #40649
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1COC2(CCN(C(=O)OCc3ccccc3)CC2)C(Cc2ccc(F)cc2)N1
Reaction #836458
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_07
O=C1COC2(CCN(C(=O)OCc3ccccc3)CC2)C(Cc2ccc(F)cc2)N1
Reaction #985464
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
O=C1COC2(CCN(C(=O)OCc3ccccc3)CC2)C(Cc2ccc(F)cc2)N1
Reaction #1159740
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_06
O=C1COC2(CCN(C(=O)OCc3ccccc3)CC2)C(Cc2ccc(F)cc2)N1
Reaction #1438418
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_05
O=C1COC2(CCN(C(=O)OCc3ccccc3)CC2)C(Cc2ccc(F)cc2)N1
Reaction #1874900
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_03