子结构搜索

CO.O

CC(C)(N)COc1ccc(O)c(C(N)=O)c1
Reaction #4638
5-(2-amino-2-methylpropoxy)salicylamide
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)c1ccc(OCc2ccccc2)cc1F
Reaction #62175
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccncc1)c1ccc(OCc2ccccc2)cc1F
Reaction #62176
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCc1ccc([N+](=O)[O-])cc1
Reaction #62263
product
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(C(=O)/C=C/C(=O)O)c2cc([N+](=O)[O-])ccc2O1
Reaction #65390
trans-4-(3,4-dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)-4-oxo-2-butenoic acid
收率 67.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(NC)C(=O)N1CC(C)(C)Oc2ccc([N+](=O)[O-])cc21
Reaction #65399
ethyl 4-(3,4-dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)-3-methylamino-4-oxobutanoate
收率 36.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)=NOCc2cccc(F)c2)cc1F
Reaction #70236
3′-fluoro-4′-methoxyacetophenone-O-3-fluorobenzyloxime
收率 90.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H]1Cc2ccccc2N(OC)C1=O
Reaction #75425
title compound
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(CCC(=O)CCc2ccccc2)[N+](=O)[O-])cc1OC
Reaction #94743
crude oil
收率 113.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(CCC2(CCc3ccccc3)OCCO2)[N+](=O)[O-])cc1OC
Reaction #94744
oil
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CC(O)CCC2[N+](=O)[O-])cc1OC
Reaction #160676
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CC(=O)CCC2[N+](=O)[O-])cc1OC
Reaction #160677
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc(C(C)(C)C)c(N)c1
Reaction #161210
(3-amino-4-tert-butyl-phenyl)-carbamic acid tert-butyl ester
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1-c1nnc(-c2nc(-c3ccc(C(=O)N(C)C)cc3)cnc2N)o1
Reaction #165801
product
收率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(-c3nnc(-c4ccccc4OCCN)o3)n2)cc1
Reaction #165807
product
收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(C2(C(=O)Nc3ccc(N4CCC(NCC(C)=O)C4)cc3)CC2)cc1
Reaction #173250
DOI: 10.1039/C8SC04228D
CC1(c2cc(Br)cc([N+](=O)[O-])c2)COCC(=O)N1
Reaction #178651
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCC(Oc2cc(C(F)(F)F)ccc2F)CC1)c1cc(-c2ccccc2)[nH]n1
Reaction #184045
DOI: 10.1039/C8SC04228D
C#Cc1cc(CNC(=O)C=Cc2ccc(C(F)(F)F)cc2OCCC)cc(F)c1NS(C)(=O)=O
Reaction #193682
DOI: 10.1039/C8SC04228D
COC(=O)c1cc([N+](=O)[O-])c(C(F)(F)F)cc1NC(C)=O
Reaction #198916
DOI: 10.1039/C8SC04228D
第 1 页下一页