بحث البنية الفرعية

Cc1nn(C)cc1N

CNC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1C#N
Reaction #129
المردود 50.0%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #131
المردود 7.3%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #132
المردود 54.9%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #133
المردود 43.8%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #134
المردود 15.6%
CONC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #146
المردود 14.3%
CNC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #157
المردود 53.3%
CONC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1C(F)(F)F
Reaction #170
المردود 11.2%
CNC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1C(F)(F)F
Reaction #172
المردود 33.7%
CNC(=O)c1ccc(F)cc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #174
المردود 3.9%
CONC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #90782
desired product
المردود 18.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C)c(C(N)=O)c1[N+](=O)[O-]
Reaction #159366
desired product
المردود 51.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C)c(C(N)=O)c1N
Reaction #159367
desired product
المردود 97.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCCC(C)(C)P1c1ccnn1-c1c(-c2ccccc2)nn(-c2ccccc2)c1-c1ccccc1
Reaction #166160
1′,3′,5′-Triphenyl-5-(2,2,6,6-tetramethylphosphinan-1-yl)-1′H-1,4′-bipyrazole
المردود 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N[SH](=O)=O)c(C(=O)NN)nn1C
Reaction #173113
DOI: 10.1039/C8SC04228D
COC(=O)c1nn(C)cc1NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #176300
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1C)C(c1ccccc1Cl)=NC1=C(C)NNC1=N2
Reaction #176353
DOI: 10.1039/C8SC04228D
O=C1c2nn(-c3ccccc3Cl)c(-c3ccc(Cl)cc3)c2NCC2CCCN12
Reaction #198968
DOI: 10.1039/C8SC04228D
CNC(=O)c1cc(F)ccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #198975
DOI: 10.1039/C8SC04228D
Cc1nn(-c2cc(OC(C)C)c(Cl)cc2F)c(C)c1N
Reaction #204845
DOI: 10.1039/C8SC04228D
الصفحة 1التالي