部分構造検索

Cc1ccc(O)cc1N

CN1CC[C@@]2(C)c3cc(Br)c(O)cc3N(C)[C@@H]12
Reaction #1864
cis-(±)-5-Bromo-1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo[2,3-b]indol-6-ol
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)=O)c(N)cc1OCc1ccccc1
Reaction #43791
product
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCCO/N=C/c2ccc(-c3ccccc3)cc2)cc1NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #57955
4-[3-({[(1E)-1,1′-biphenyl-4-ylmethylidene]amino}oxy)propoxy]-2-{[4-(trifluoromethoxy)benzoyl]amino}benzoic acid methyl ester
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(OCCCO/N=C/c2ccc(-c3ccccc3)cc2)ccc1C(=O)O)c1ccc(OC(F)(F)F)cc1
Reaction #57956
4-[3-({[(1E)-1,1′-biphenyl-4-ylmethylidene]amino}oxy)propoxy]-2-{[4-(trifluoromethoxy)benzoyl]amino}benzoic acid
収率 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCCO/N=C/c2ccc(C(F)(F)F)cc2)cc1NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #57957
2-{[4-(trifluoromethoxy)benzoyl]amino}-4-{3-[({(1E)-[4-(trifluoromethyl)phenyl]methylidene}amino)oxy]propoxy}benzoic acid methyl ester
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(OCCCO/N=C/c2ccc(-c3ccccc3)cc2)ccc1C(=O)O)c1ccc(OC(F)(F)F)cc1
Reaction #57958
4-[3-({[(1E)-1,1′-biphenyl-4-ylmethylidene]amino}oxy)propoxy]-2-{[4-(trifluoromethoxy)benzoyl]amino}benzoic acid
収率 192.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCCO/N=C/c2ccc(C(C)(C)C)cc2)cc1NC(=O)c1ccc(-c2ccccc2)cc1
Reaction #57973
2-[(1,1′-biphenyl-4-ylcarbonyl)amino]-4-[3-({[(1E)-(4-tert-butylphenyl)methylidene]amino}oxy)propoxy]benzoic acid methyl ester
収率 131.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(/C=N/OCCCOc2ccc(C(=O)O)c(NC(=O)c3ccc(-c4ccccc4)cc3)c2)cc1
Reaction #57974
2-[(1,1′-biphenyl-4-ylcarbonyl)amino]-4-[3-({[(1E)-(4-tert-butylphenyl)methylidene]amino}oxy)propoxy]benzoic acid
収率 63616.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)N(CCN1CCC(NCc3ccc4c(c3)OCCO4)CC1)C(=O)CC2.Cl
Reaction #68288
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-3,4-dihydroquinolin-2(1H)-one hydrochloride
収率 135.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(-c3cccc([N+](=O)[O-])c3)[nH]c(=O)c2cc1OCc1ccccc1
Reaction #89922
6-(benzyloxy)-7-methoxy-2-(3-nitrophenyl)quinazolin-4(3H)-one
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)C)c([N+](=O)[O-])cc1O
Reaction #161166
2,4-di-tert-butyl-5-nitro-phenol
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)C)c(O)cc1N
Reaction #161167
5-amino-2,4-di-tert-butyl-phenol
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1-c1cc(C(C)(C)C)c(O)cc1N
Reaction #161186
2-tert-butyl-4-(2-ethoxyphenyl)-5-aminophenol
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc(-c2cc(C(C)(C)C)c(O)cc2N)c1
Reaction #161187
2-tert-Butyl-4-(3-ethoxyphenyl)-5-aminophenol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)c1cc(C(C)(C)C)c([N+](=O)[O-])cc1O
Reaction #163962
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)CO)c(O)cc1[N+](=O)[O-]
Reaction #163963
4-tert-butyl-2-(1-hydroxy-2-methylpropan-2-yl)-5-nitrophenol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)C)c([N+](=O)[O-])cc1O
Reaction #173238
DOI: 10.1039/C8SC04228D
COC(=O)C=C(Nc1cc(CCCl)c([N+](=O)[O-])cc1OCc1ccccc1)C(F)(F)F
Reaction #174845
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)Nc2cc(NC(=O)c3ccccc3)ccc2Cl)c(N)c1
Reaction #178061
DOI: 10.1039/C8SC04228D
Cc1nc(C(=O)Nc2cc(Oc3ccc4nc(NC(=O)C5CC5)nn4c3)ccc2C)c(C)o1
Reaction #182022
DOI: 10.1039/C8SC04228D
1 ページ次のページ