Поиск по сходству

18

CN(C)CCNc1ccccc1
Reaction #231
Выход 0.0%
CC(=O)Nc1cnc(N2CCN(C)CC2)cn1
Reaction #299
Выход 79.5%
O=C1NCCc2cc(NCc3ccccc3)ccc21
Reaction #341
Выход 0.0%
O=C1NCCc2cc(NCc3ccccc3)ccc21
Reaction #343
Выход 0.0%
Cc1cccc(C)c1C(=O)NC(c1ccc(N2CCOCC2)cc1)C12CCC(CC1)N2C
Reaction #359
Выход 29.6%
CC(C)(C)OC(=O)N1CCN(c2cccs2)CC1
Reaction #398
Выход 0.0%
COC(=O)Cc1cc(N2CC(F)(F)C2)ccn1
Reaction #652
Выход 39.9%
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ncc1C
Reaction #821
Выход 10.6%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #833
Выход 0.0%
Cc1cc(C=O)c(C)c2c1SCCC2(C)C
Reaction #894
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(Oc2cccc(C(F)(F)F)c2)nc(SC)n1
Reaction #897
4-ethoxy-2-methylthio-6-[3-(trifluoromethyl)phenoxy]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1
Reaction #908
N-(1,1-Dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1C=O
Reaction #916
title compound
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(Sc2ccccc2)cccc1[N+](=O)[O-]
Reaction #929
2-nitro-6-(phenylthio)benzonitrile
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)cc(Sc2cccc([N+](=O)[O-])c2C#N)c1
Reaction #931
2-[(3,5-dimethylphenyl)thio]-6-nitrobenzonitrile
Выход 73011.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN=[N+]=[N-])cc1
Reaction #951
4-cyanobenzyl azide
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #956
4-Azidoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCC1CCN(C(=N)NC(=O)OCc2ccccc2)C1
Reaction #960
product
Выход 68.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c[nH]c2c1C(=O)CCC2
Reaction #997
ethyl 4-oxo-4,5,6,7-tetrahydroindole-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c[nH]c2c1C(=O)CCCC2
Reaction #1001
ethyl 4-oxo-1,4,5,6,7,8-hexahydro-cyclohepta[b]pyrrole-3-carboxylate
Выход 50.7%DOI: 10.6084/m9.figshare.5104873.v1
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