Поиск подструктуры

1446

O=C(Nc1cccc(I)c1)c1ccccc1SSc1ccccc1C(=O)Nc1cccc(I)c1
Reaction #3830
title compound
Выход 7.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)Nc2cccc(I)c2)ccc1OCCNC(=O)OC(C)(C)C
Reaction #7153
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)Nc2cccc(-c3ccccc3)c2)ccc1OCCNC(=O)OC(C)(C)C
Reaction #7168
4-[2-(tert-butoxycarbonylamino)ethoxy]-3-methoxy-N-(3-phenylphenyl)phenylacetamide
Выход 77.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)Nc2cccc(/C=C/c3cccc(C)c3)c2)ccc1OCCNC(=O)OC(C)(C)C
Reaction #7178
4-[2-(tert-butoxycarbonylamino)-ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide
Выход 152.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(I)c(O)c([N+](=O)[O-])c1
Reaction #42461
title compound
Выход 91075.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N)c(O)c(I)c1
Reaction #42462
title compound
Выход 92.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc(CCC=O)c1
Reaction #44177
title compound
Выход 60.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2ncnc(Nc3cccc(I)c3)c2cn1
Reaction #79073
7-amino-4-(3-iodoanilino)pyrido[4,3-d]pyrimidine
Выход 61.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86675
compound ( 4a )
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86676
compound ( 4a )
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(I)c(C)c([N+](=O)[O-])c1
Reaction #88078
3-iodo-4-methyl-5-nitro-benzoic acid methyl ester
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N)c(C)c(I)c1
Reaction #88079
3-amino-5-iodo-4-methyl-benzoic acid methyl ester
Выход 67.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N)c(N)c(I)c1
Reaction #88083
3,4-diamino-5-iodo-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(I)c2nc[nH]c2c1
Reaction #88084
7-Iodo-3H-benzoimidazole-5-carboxylic acid methyl ester
Выход 45.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(-c2cccnc2)ccc1S(=O)(=O)c1ccccc1
Reaction #159820
3-(3-nitro-4-(phenylsulfonyl)phenyl)pyridine
Выход 70.5%DOI: 10.6084/m9.figshare.5104873.v1
COCC(C)NC(=O)c1cc(I)cc([N+](=O)[O-])c1
Reaction #164936
3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamide
Выход 27.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(I)cc([N+](=O)[O-])c1F
Reaction #164945
2-fluoro-5-iodo-3-nitro-benzoic acid methyl ester
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(I)cc(N)c1F
Reaction #164946
3-amino-2-fluoro-5-iodo-benzoic acid methyl ester
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC(C)NC(=O)c1cc(I)cc([N+](=O)[O-])c1
Reaction #171914
3-Iodo-N-(2-methoxy-1-methyl-ethyl)-5-nitro-benzamide
Выход 27.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc[nH]c1C=C1C(=O)Nc2ccc(F)c(C#CCN3CCOCC3)c21
Reaction #173539
DOI: 10.1039/C8SC04228D
Страница 1Далее