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NOCc1ccc(Cl)s1

CC(=O)OC1=C(C(C)=NOCc2ccc(Cl)s2)C(=O)CC(C2CCCSC2)C1
Reaction #256729
DOI: 10.1039/C8SC04228D
CC(=NOCc1ccc(Cl)s1)c1cc(Cl)ccc1NS(=O)(=O)C(F)(F)F
Reaction #689782
N-{4-chloro-2-[1-(5-chlorothiophen-2-ylmethoxyimino)ethyl]phenyl}trifluoromethanesulfonamide
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=NOCc1ccc(Cl)s1)C1=C(O)CC(C2CCCSC2)CC1=O
Reaction #708552
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1=C(C(C)=NOCc2ccc(Cl)s2)C(=O)CC(C2CCCSC2)C1
Reaction #708553
title compound
Ausbeute 61.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1=C(C(C)=NOCc2ccc(Cl)s2)C(=O)CC(C2CCCSC2)C1
Reaction #708555
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=NOCc1ccc(Cl)s1)C1=C(O)CC(C2CCCSC2)CC1=O
Reaction #916845
DOI: 10.1039/C8SC04228D
CC(=NOCc1ccc(Cl)s1)c1cc(Cl)ccc1NS(=O)(=O)C(F)(F)F
Reaction #1058041
N-{4-chloro-2-[1-(5-chlorothiophen-2-ylmethoxyimino)ethyl]phenyl}trifluoromethanesulfonamide
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=NOCc1ccc(Cl)s1)C1=C(O)CC(C)(C)CC1=O
Reaction #1222848
DOI: 10.1039/C8SC04228D
CCC(=NOCc1ccc(Cl)s1)C1=C(O)CC(C)(C)CC1=O
Reaction #1475821
2-{1-[(5-chlorothien-2-ylmethoxy)imino]propyl}-3-hydroxy-5,5-dimethylcyclohex-2-en-1-one
Ausbeute 70.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=NOCc1ccc(Cl)s1)C1=C(OC(C)=O)CC(C)(C)CC1=O
Reaction #1475822
3-acetyloxy-2-{1-[(5-chlorothien-2-ylmethoxy)imino]butyl}-5,5-dimethylcyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1
NOCc1ccc(Cl)s1
Reaction #1750302
O-(5-Chloro-thiophen-2-ylmethyl)-hydroxylamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NOCc1ccc(Cl)s1)c1ccccc1NCc1ccncc1
Reaction #1750333
N-(5-Chloro-thiophen-2-ylmethoxy)-2-[(pyridin-4-ylmethyl)-amino]-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1=C(C(C)=NOCc2ccc(Cl)s2)C(=O)CC(C2CCCSC2)C1
Reaction #1848983
title compound
Ausbeute 61.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1=C(C(C)=NOCc2ccc(Cl)s2)C(=O)CC(C2CCCSC2)C1
Reaction #1848984
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=NOCc1ccc(Cl)s1)C1=C(O)CC(C2CCCSC2)CC1=O
Reaction #1848985
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NOCc1ccc(Cl)s1)c1ccccc1NCc1ccncc1
Reaction #2228929
DOI: 10.1039/C8SC04228D
CC(=NOCc1ccc(Cl)s1)c1cc(Cl)ccc1NS(=O)(=O)C(F)(F)F
Reaction #2233850
DOI: 10.1039/C8SC04228D
CC(=O)OC1=C(C(C)=NOCc2ccc(Cl)s2)C(=O)CC(C2CCCSC2)C1
Reaction #2248527
DOI: 10.1039/C8SC04228D