子结构搜索

650

COc1cc(N2CCN(C(=O)OC(C)(C)C)CC2=O)ccc1[N+](=O)[O-]
Reaction #279
收率 68.4%
COc1cc(N2CCN(C(=O)OC(C)(C)C)CC2=O)ccc1[N+](=O)[O-]
Reaction #280
收率 100.3%
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])c(OC)c2)cc1
Reaction #9652
methyl 4-(3′-methoxy4′-nitro-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
收率 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(Cl)ccc1[N+](=O)[O-]
Reaction #48559
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])c(OC)c2)cc1
Reaction #59149
methyl 4-(3′-methoxy-4′-nitro-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
收率 48.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2=CCN(C(=O)OC(C)(C)C)CC2)ccc1[N+](=O)[O-]
Reaction #88645
4-(3-methoxy-4-nitro-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Oc2cc(C)[nH]n2)ccc1[N+](=O)[O-]
Reaction #183258
DOI: 10.1039/C8SC04228D
COc1cc(Cl)c(C(F)(F)F)cc1N
Reaction #194875
DOI: 10.1039/C8SC04228D
C=CCOc1cc(Cl)c(C)cc1[N+](=O)[O-]
Reaction #196912
DOI: 10.1039/C8SC04228D
Cc1cc([N+](=O)[O-])c2c(c1Cl)CC(CO)O2
Reaction #202897
DOI: 10.1039/C8SC04228D
O=C(O)c1ccccc1Oc1cc(Cl)ccc1[N+](=O)[O-]
Reaction #209254
DOI: 10.1039/C8SC04228D
COc1cccc(Oc2cc(Cl)c(Cl)cc2[N+](=O)[O-])c1OC
Reaction #219022
4,5-Dichloro-2-(2,3-dimethoxyphenoxy)-1-nitrobenzene
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)ccc1NC(=O)C(C)(C)C
Reaction #228026
DOI: 10.1039/C8SC04228D
COc1c([N+](=O)[O-])cc(C=O)c(Cl)c1O
Reaction #235356
DOI: 10.1039/C8SC04228D
CC1COc2c(ccc(Cl)c2F)N1
Reaction #245244
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCc2c(cccc2Oc2cc(Cl)ccc2N)C1
Reaction #246066
DOI: 10.1039/C8SC04228D
Cn1c(C(F)(F)F)ccc(-c2cc([N+](=O)[O-])c(O)cc2Cl)c1=O
Reaction #247875
DOI: 10.1039/C8SC04228D
COc1c(N)ccc(Cl)c1C(F)(F)F
Reaction #248773
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(Cl)cc1O
Reaction #249366
DOI: 10.1039/C8SC04228D
CC1Oc2cc(Cl)c(-c3ccc(C(F)(F)F)n(C)c3=O)cc2NC1=O
Reaction #251282
DOI: 10.1039/C8SC04228D
第 1 页下一页