بحث البنية الفرعية

16760302

COC(=O)c1cc(Br)ccc1N1CCOCC1
Reaction #501
المردود 17.9%
O=C(OCc1ccccc1)c1cc(Br)cc2c1NCCCC2
Reaction #5028
compound
المردود 99.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)cc([N+](=O)[O-])c1N
Reaction #40531
title compound
المردود 87.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C2CC2)ccc1N
Reaction #70276
expected product
المردود 88.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C2CC2)ccc1N
Reaction #70315
expected product
المردود 88.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Br)cc1CO
Reaction #72467
(2-amino-5-bromophenyl)methanol
المردود 59.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(Cl)cc2)ccc1N
Reaction #159380
4-Amino-4′-chlorobiphenyl-3-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(C(=O)O)cc(Br)c2ccccc12
Reaction #169619
1-amino-4-bromo-2-naphthoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cc2ccc(Cl)cc2)c2ccccc2c1N
Reaction #169648
methyl 1-amino-4-(4-chlorobenzyl)-2-naphthoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)c2ccccc2c1/N=C/N(C)C
Reaction #169653
methyl 4-bromo-1-{[(1E)-(dimethylamino)methylene]amino}-2-naphthoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)ccc1N
Reaction #182219
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(Br)cc2c1N(C(=O)OC(C)(C)C)CC2
Reaction #195085
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(C#C[Si](C)(C)C)c(F)c(F)c1Nc1ccccc1F
Reaction #200908
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(-c2cccnc2)ccc1NC(=O)COCC(=O)N1CCN(C(c2ccccc2)c2ccccc2)CC1
Reaction #201252
DOI: 10.1039/C8SC04228D
Cc1cc(Br)cc(C(=O)OC(C)(C)C)c1N
Reaction #207398
DOI: 10.1039/C8SC04228D
NC(=O)c1cc(Br)c([N+](=O)[O-])cc1N
Reaction #227760
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(Br)ccc1NC(=O)OC(C)C
Reaction #231762
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(Br)ccc1NC(=O)COCC(=O)O
Reaction #235515
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(-c2ccc(C#N)cc2)ccc1NC(=O)COCC(=O)N1CCN(C(c2ccccc2)c2ccccc2)CC1
Reaction #241262
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(C#C[Si](C)(C)C)c(F)c(F)c1Nc1ccccc1F
Reaction #241714
DOI: 10.1039/C8SC04228D
الصفحة 1التالي