部分構造検索

3758

N#CCCCCC(N)=O
Reaction #2051
desired product
DOI: 10.6084/m9.figshare.5104873.v1
N#CCCCCC(N)=O
Reaction #2052
5-cyanopentanamide
DOI: 10.6084/m9.figshare.5104873.v1
N#CCCCC1C(=O)NCCNCCCNCCNC1=O
Reaction #74919
3-(3-cyanopropyl)-2,4-dioxo-1,5,8,12-tetraaza-cyclotetradecane
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCC(=O)N1C(CO)c1cc(F)c(F)c(F)c1
Reaction #178960
DOI: 10.1039/C8SC04228D
N#CCCCC1C(=O)NCCNCCCNCCNC1=O
Reaction #243413
DOI: 10.1039/C8SC04228D
N#CCCCC1Sc2ccccc2NC1=O
Reaction #271135
DOI: 10.1039/C8SC04228D
NCCCCCC(N)=O
Reaction #272466
DOI: 10.1039/C8SC04228D
CN(CC(=O)c1ccc(OCC(=O)O)c(OCC(=O)O)c1)C(=O)[C@H]1CC[C@H](C(N)=S)CC1
Reaction #321333
thioamide
DOI: 10.6084/m9.figshare.5104873.v1
N#CCCCC1Sc2ccccc2NC1=O
Reaction #322825
2-(3-cyanopropyl)-2H-1,4-benzothiazin-3(4H)-one
収率 66.8%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@]1(F)[C@@H]2C[C@@H](OCc3ccc(Cl)c(Cl)c3)C(=O)[C@@H]21
Reaction #326271
(1R,3R,5R,6R)-3-[(3,4-dichloro benzyl)oxy]-6-fluoro-2-oxo bicyclo[3.1.0]hexane-6-carboxamide
収率 977.1%DOI: 10.6084/m9.figshare.5104873.v1
N#C[C@@]1(N)[C@H]2[C@@H](C[C@H]1OCc1ccc(Cl)c(Cl)c1)[C@]2(F)C(N)=O.O=C(O)[C@H](O)[C@@H](O)C(=O)O
Reaction #326272
(1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamide L-tartarate
DOI: 10.6084/m9.figshare.5104873.v1
N#C[C@@]1(N)[C@H]2[C@@H](C[C@H]1OCc1ccc(Cl)c(Cl)c1)[C@]2(F)C(N)=O.O=C(O)C(=O)O
Reaction #326273
(1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluorobicyclo[3.1.0]hexane-6-carboxamide oxalate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.N#C[C@@]1(N)[C@H]2[C@@H](C[C@H]1OCc1ccc(Cl)c(Cl)c1)[C@]2(F)C(N)=O
Reaction #326274
(1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamide p-toluene sulfonate
DOI: 10.6084/m9.figshare.5104873.v1
N#C[C@@]1(N)[C@H]2[C@@H](C[C@H]1OCc1ccc(Cl)c(Cl)c1)[C@]2(F)C(=O)O
Reaction #326275
(1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@]1(N)[C@H]2[C@@H](C[C@H]1OCc1ccc(Cl)c(Cl)c1)[C@]2(F)C(N)=O
Reaction #326276
(1R, 2R,3R,5R,6R)-2-amino-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-2,6-dicarboxamide
収率 324.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)CCC(C(C#N)=Cc1cc(Oc2ccccc2)ccc1[N+](=O)[O-])C1CCOCC1)C1CCCCC1
Reaction #339624
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)CCC(c1cc2cc(Oc3ccccc3)ccc2nc1N)C1CCOCC1)C1CCCCC1
Reaction #339625
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc([N+](=O)[O-])c(C=C(C#N)C(CCC(=O)NCCC(C)(C)C)C2CCOCC2)cc1Oc1ccccc1
Reaction #339652
5-Cyano-6-(4-ethoxy-2-nitro-5-phenoxy-phenyl)-4-(tetrahydro-pyran-4-yl)-hex-5-enoic acid (3,3-dimethyl-butyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc2nc(N)c(C(CCC(=O)NCCC(C)(C)C)C3CCOCC3)cc2cc1Oc1ccccc1.Cl
Reaction #339653
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCC(N)=O
Reaction #392273
DOI: 10.1039/C8SC04228D
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