Ähnlichkeitssuche

8778

COC(=O)c1cccc(C=CC(=O)c2cccc(OCc3ccccc3)c2)c1
Reaction #6471
1-(3-Benzyloxyphenyl)-3-(3-(methoxycarbonyl)phenyl)-2-propen-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C(Cc1ccc2ccccc2c1)N1CCN(C(=O)C(Cc2ccc(F)cc2)NC(=O)C(Cc2ccc(O)cc2)NC(C)=O)C(CCO)C1
Reaction #8630
desired product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(NC(=O)c2cnccn2)n(-c2c(Cl)cc(C(F)(F)F)cc2Cl)n1
Reaction #51141
N-[3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole-5-yl]pyrazine-2-carboxamide
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CSCc1ccc(Cl)cc1)NO
Reaction #55076
p-Chlorobenzylmercapto-acetohydroxamic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CSCc1ccc(Cl)cc1)NO
Reaction #56444
p-Chlorobenzylmercapto-acetohydroxamic acid
DOI: 10.6084/m9.figshare.5104873.v1
CN(CC1CO1)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #59222
N-glycidyl-N-methylperfluorobutanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
c1cnc(-c2ncc[nH]2)nc1
Reaction #73096
2-(1H-imidazol-2-yl)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ocnc1C(=N)N
Reaction #91961
5-methyloxazole-4-carboxamidine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1
Reaction #172193
methyl benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)c1ccc(Cl)cc1C(F)(F)F
Reaction #172289
4-chloro-1-(dimethoxymethyl)-2-(trifluoromethyl)benzene
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)nc(N)n1
Reaction #323704
product
Ausbeute 58.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(c1nc2ccccc2c(=O)[nH]1)C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #325419
product
Ausbeute 5.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c(=S)n(Cc2cc(F)ccc2Br)c1=O
Reaction #327461
4-(2-bromo-5-fluorobenzyl)-6-methyl-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c(=S)n(Cc2cc(F)ccc2Cl)c1=O
Reaction #327473
4-(2-chloro-5-fluorobenzyl)-6-methyl-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=Cc1ccc(C(=O)C=Cc2sc3cc(C(F)(F)F)ccc3c2C)cc1C
Reaction #328546
titled compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(-c2ccccc2)nc2cc(Cl)ccc12
Reaction #331398
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(=O)N[C@@H](C)C(=O)O)c(O)c2ccc(Oc3ccc(F)cc3)cc12
Reaction #337539
title compound
Ausbeute 71.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)c1ncc2cc(Oc3ccc(F)cc3)ccc2c1O)C(=O)O
Reaction #337541
title compound
Ausbeute 49.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(=O)N[C@@H](C)C(=O)O)c(O)c2ccc(Oc3ccccc3)cc12
Reaction #337543
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(O)c2ccccc2c1OCc1ccccc1
Reaction #337617
yellow solid
Ausbeute 30.7%DOI: 10.6084/m9.figshare.5104873.v1
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