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16615

C#CCOC(=NOC)c1ccc(Cl)cc1Cl
Reaction #3501
propargyl N-methoxy-2,4-dichlorobenzimidate
Выход 29.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])cc1Cl)N1CCc2cccn2-c2ccccc21
Reaction #3702
yellow foam
Выход 105.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nn(-c2cccc([N+](=O)[O-])c2)c1C
Reaction #8154
3,5-dimethyl-1-(3-nitrophenyl)-1H-pyrazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c1Cl.[Br-]
Reaction #11175
phosphonium
Выход 44.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CN(O)CCNC(=O)c1cccc(Cl)c1Cl
Reaction #52093
title compound
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CN(O)CCNC(=O)c1cc(Cl)ccc1Cl
Reaction #52099
title compound
Выход 33.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CN(O)CCNC(=O)c1cc(Br)ccc1Cl
Reaction #52102
title compound
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52570
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52571
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
Выход 44.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=S)SC(C[N+](=O)[O-])c1cc([N+](=O)[O-])ccc1Cl
Reaction #54422
2-chloro-5-nitro-α-(nitromethyl)benzyl dimethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #54983
N-ethyl-4-chloro-2-nitro-aniline
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CSCc1ccc(Cl)cc1)NO
Reaction #55076
p-Chlorobenzylmercapto-acetohydroxamic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Nc1ccc(C(=O)NCC(=O)NO)cc1
Reaction #55084
4-Amino-benzamido-acetohydroxamic acid hydrochloride
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)CC1Oc2ccc(Cl)cc2C(=O)N1O
Reaction #56156
6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-4H-1, 3-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC2Oc3ccc(Cl)cc3C(=O)N2O1
Reaction #56157
7-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one
Выход 57.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)CC1Oc2ccc(Cl)cc2C(=O)N1O
Reaction #56250
6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-4H-1,3-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC2Oc3ccc(Cl)cc3C(=O)N2O1
Reaction #56251
7-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one
Выход 57.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC2Oc3ccc(Cl)cc3C(=O)N2O1
Reaction #56252
7-chloro-2-methyl-3,3a-dihydro-2H, 9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CSCc1ccc(Cl)cc1)NO
Reaction #56444
p-Chlorobenzylmercapto-acetohydroxamic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CS(=O)Cc1ccc(Cl)cc1)NO
Reaction #56445
α-(p-Chlorobenzylsulphinyl)-acetohydroxamic acid
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
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