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CNC(C)c1ccccc1

Cc1ccccc1S(=O)(=O)n1ccc2c([C@@]34CN[C@H](CN3C)C4)cccc21
Reaction #8430
white solid
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(=O)N[C@@H](C)c2ccc(C)cc2)s1
Reaction #11526
(S)-5-(1-p-Tolyl-ethylcarbamoyl)-thiophene-2-carboxylic acid methyl ester
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(NC(=O)C1CC(=O)N(c2cccc(NC(=O)NCc3cccs3)c2)C1)c1cc(Cl)cc(Cl)c1O
Reaction #51182
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNc1cccc(C(=C2CN(C(c3ccccc3)c3ccccc3)C2)S(C)(=O)=O)c1
Reaction #53463
1-benzhydryl-3-[(3-methylaminophenyl)(methylsulfonyl)methylene]azetidine
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1
CNCC(=O)N1CCN(c2cccc(CS(=O)(=O)C=C3CN(C(c4ccc(Cl)cc4)c4ccc(Cl)cc4)C3)c2)CC1
Reaction #53503
1-{4-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)phenyl]piperazin-1-yl}-2-methylaminoethanone
Ausbeute 83.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(=O)N1CCN(c2cccc(CS(=O)(=O)C=C3CN(C(c4ccc(Cl)cc4)c4ccc(Cl)cc4)C3)c2)CC1)C(=O)OC(C)(C)C
Reaction #53504
(2-{4-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)phenyl]piperazin-1-yl}-2-oxoethyl)-N-methylcarbamic acid tert-butyl ester
Ausbeute 100.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N1CCN(c2cccc(CS(=O)(=O)C=C3CN(C(c4ccc(Cl)cc4)c4ccc(Cl)cc4)C3)c2)CC1
Reaction #53507
4-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)phenyl]piperazine-1-carboxylic acid methyl ester
Ausbeute 103.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N(CC1NCCc2cc(O)c(O)cc21)c1ccc(Cl)cc1.Cl
Reaction #55427
1-(N-ethoxycarbonyl-p-chloroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1c2ccccc2-c2ccc(F)cc2N1S(=O)(=O)c1cccc(O)c1
Reaction #173679
DOI: 10.1039/C8SC04228D
CCC1c2cc(F)ccc2-c2cc(C)ccc2N1S(=O)(=O)c1ccc(OC)cc1
Reaction #175822
DOI: 10.1039/C8SC04228D
CCC1c2cc(F)ccc2-c2ccccc2N1S(=O)(=O)c1ccc(O)cc1
Reaction #176371
DOI: 10.1039/C8SC04228D
CC1c2cc(Cl)ccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(O)cc1
Reaction #178693
DOI: 10.1039/C8SC04228D
Cc1ccc(F)cc1C1NC(=O)CC(c2cc(Cl)ccc2OC2(C(=O)NS(=O)(=O)c3ccc(F)cc3)CCC2)C12C(=O)Nc1cc(Cl)ccc12
Reaction #182212
DOI: 10.1039/C8SC04228D
CCC1c2ccccc2-c2sc(-c3ccsc3)cc2N1S(=O)(=O)c1ccc(OC)cc1
Reaction #183066
DOI: 10.1039/C8SC04228D
CCC1c2c(C)cccc2-c2ccccc2N1S(=O)(=O)c1ccc(O)cc1
Reaction #188529
DOI: 10.1039/C8SC04228D
Cc1sc(NC(=O)COCC(=O)N2CCN(C(c3ccccc3)c3ccccc3)CC2)c(C(=O)O)c1-c1ccncc1
Reaction #191899
DOI: 10.1039/C8SC04228D
CN(CC(=O)N1CCN(c2cccc(CS(=O)(=O)C=C3CN(C(c4ccc(Cl)cc4)c4ccc(Cl)cc4)C3)c2)CC1)C(=O)OC(C)(C)C
Reaction #193178
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(C(=O)NC(C)c2cccc(Br)c2)s1
Reaction #196670
DOI: 10.1039/C8SC04228D
Cc1sc(NC(=O)COCC(=O)N2CCN(C(c3ccccc3)c3ccccc3)CC2)c(C(=O)[O-])c1-c1ccccc1
Reaction #197186
DOI: 10.1039/C8SC04228D
CCC1c2cc(F)ccc2-c2ccccc2N1S(=O)(=O)c1ccc(O)c(Cl)c1
Reaction #198024
DOI: 10.1039/C8SC04228D
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