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73767

Cc1ccc(-c2cccc(C(O)Cc3cc(Cl)c4cccnc4c3OCc3ccccc3)c2)s1
Reaction #205003
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2cccc(C(O)Cc3cc(Cl)c4cccnc4c3OCc3ccccc3)c2)s1
Reaction #638306
final product
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC(Cc1cc(Cl)c2cccnc2c1OCc1ccccc1)c1cccc(CN2CCCC2)c1
Reaction #638310
N-[2-(8-benzyloxy-5-chloro-quinolin-7-yl)-1-(3-pyrrolidin-1-ylmethyl-phenyl)-ethyl]-2-phenoxy-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccc(C(Cc3cc(Cl)c4cccnc4c3O)NC(=O)COc3ccccc3)c2)s1
Reaction #638313
title compound
Ausbeute 84.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccc(C(Cc3cc(Cl)c4cccnc4c3O)NC(=O)COCc3ccccc3)c2)s1
Reaction #638314
title compound
Ausbeute 57.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccc(C(Cc3cc(Cl)c4cccnc4c3O)NC(=O)C(C)(C)Oc3ccc(Cl)cc3)c2)s1
Reaction #638315
title compound
Ausbeute 132.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccc(C(Cc3cc(Cl)c4cccnc4c3O)NC(=O)COc3ccc(C(C)(C)C)cc3)c2)s1
Reaction #638316
title compound
Ausbeute 126.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccc(C(Cc3cc(Cl)c4cccnc4c3OCc3ccccc3)NC(=O)C(C)(C)Oc3ccc(Cl)cc3)c2)s1
Reaction #889283
DOI: 10.1039/C8SC04228D
O=C(COc1ccccc1)NC(Cc1cc(Cl)c2cccnc2c1OCc1ccccc1)c1cccc(CN2CCCC2)c1
Reaction #2410182
DOI: 10.1039/C8SC04228D