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164800

CN1Cc2c(Br)cc3c(c2C1)NC(=O)C3=O
Reaction #5033
5-bromo-1,6,7,8-tetrahydro-7-methylbenzo[2,1-b:3,4-c']dipyrrole-2,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C#N)c(C)c(Br)c1F
Reaction #45580
compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C#N)c(C)c(-c2ccccc2)c1F
Reaction #45581
4-Amino-3-cyano-6-fluoro-5-methoxy-2-methylbiphenyl
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(F)c(O)c(N)c1C#N
Reaction #45605
compound
Ausbeute 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1c(N)c(C#N)c(C)c(Br)c1F
Reaction #45606
compound
Ausbeute 97.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45607
6-Bromo-2-cyclopropyl-7-fluoro-5-methyl-1,3-benzoxazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(C#N)c(C)c(Br)c(F)c2o1
Reaction #45635
compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(F)c(O)c(NC(=O)C(C)(C)COCc2ccccc2)c1C#N
Reaction #45641
compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(F)c(O)c(NC(=O)C(C)(C)CO)c1C#N
Reaction #45642
compound
Ausbeute 50.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(F)c2oc(C(C)(C)CO)nc2c1C#N
Reaction #45643
compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc2c(C#N)c(C)c(Br)c(F)c2o1
Reaction #45670
compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(F)c2oc(Cl)nc2c1C#N
Reaction #45715
compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(F)cc(N)c1C#N
Reaction #45828
compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(F)c([N+](=O)[O-])c(N)c1C#N
Reaction #45829
2-Amino-5-bromo-4-fluoro-6-methyl-3-nitrobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(N2CC[C@H](N(C)C)C2)c([N+](=O)[O-])c(N)c1C#N
Reaction #45830
compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c([N+](=O)[O-])c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45831
compound
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C#N)CC(c2cccc(Cl)c2)=C(F)C(O)=C1N
Reaction #45877
compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Br)c2c1C(=O)NC2=O
Reaction #49271
3-amino-6-bromophthalimide
Ausbeute 74.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(N)c3c2C(=O)NC3=O)cc2ccccc21
Reaction #49272
3-amino-6-[1-(tert-butoxycarbonyl)indol-2-yl]phthalimide
Ausbeute 67.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(I)cc(Br)c2c1C(=O)NC2=O
Reaction #49274
3-amino-4-iodo-6-bromophthalimide
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
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