بحث البنية الفرعية

1276

Cc1ccccc1CC(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #3612
desired product
المردود 53.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(C)=O)C(=O)Cc1ccccc1C
Reaction #54505
ethyl 2-acetyl-4-(2-methylphenyl)-3-oxobutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CC2c3ccccc3C1(C(=O)Cl)c1ccccc12
Reaction #56228
12-acetoxy-9,10-dihydro-9,10-ethanoanthracene-9-carboxylic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC=C(C(=O)Cl)c1ccccc1COC
Reaction #64883
title compound
المردود 96.5%DOI: 10.6084/m9.figshare.5104873.v1
CC=C(C(=O)NC)c1ccccc1COC
Reaction #64884
title compound
المردود 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)=NN(C)C(=O)Cc1c(CC)cc(C)cc1CC
Reaction #72481
title compound
المردود 49.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1CC(=O)Cl
Reaction #83440
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1CC(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #83441
desired product
المردود 53.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1CC(=O)N(Cc1ccccc1)Cc1ccc(-c2ccccc2S(=O)(=O)N=CN(C)C)cc1
Reaction #179040
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)C(=O)CC2C(=O)N1CCN(C)CC1CN1CCCC1
Reaction #196023
DOI: 10.1039/C8SC04228D
Cc1ccccc1CC(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cn1
Reaction #223405
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)=NN(C)C(=O)Cc1c(CC)cc(C)cc1CC
Reaction #227204
DOI: 10.1039/C8SC04228D
O=C(Cl)Cc1ccccc1CBr
Reaction #232513
DOI: 10.1039/C8SC04228D
Cc1ccccc1CC(=O)NC(C)(C)c1ccc(F)cc1
Reaction #236979
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(OC(=O)Cc2c(C)cc(C)cc2C)CCN(OC)CC1
Reaction #244956
DOI: 10.1039/C8SC04228D
Cc1ccccc1CC(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #249179
DOI: 10.1039/C8SC04228D
Cc1cc(C)c(C2CC2)cc1CC(=O)Cl
Reaction #250072
DOI: 10.1039/C8SC04228D
Cc1ccccc1C(=O)C(=O)Cl
Reaction #264154
DOI: 10.1039/C8SC04228D
CON1CCC(C#N)(OC(=O)Cc2c(C)cc(C)cc2C)CC1
Reaction #264617
DOI: 10.1039/C8SC04228D
Cc1ccccc1CC(=O)Cl
Reaction #280294
DOI: 10.1039/C8SC04228D
الصفحة 1التالي