Busqueda de Subestructura

6463

C=CCC(=O)CNC(=O)OCC1c2ccccc2-c2ccccc21
Reaction #1845
Fmoc-Gly-Allyl
DOI: 10.6084/m9.figshare.5104873.v1
N=C(NC(=O)OCC(Cl)(Cl)Cl)c1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #2848
title compound
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4535
3-acetoxymethyl-5-dichloromethyl-2-phthalimidopyrazine
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4536
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Rendimiento 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4537
colorless crystals
Rendimiento 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C1N=CC(C(Cl)Cl)=NC1=NO
Reaction #4538
colorless crystals
Rendimiento 67.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4540
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Rendimiento 47.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7122
(1S,2R)-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide
Rendimiento 53.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)Nc1ccccc1)CC2
Reaction #11064
18b
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)N=[N+]=[N-]
Reaction #11067
intermediate
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(N(Cc4cccc(C(F)(F)F)c4)C(=O)OCc4ccccc4)c(=O)n32)cc1
Reaction #11083
intermediate 25b
Rendimiento 79.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H]1C[C@@H](C(=O)NCc2ccc(C(=N)NC(=O)OCc3ccccc3)cc2)n2c1ncc(N(CC=C)C(=O)OCc1ccccc1)c2=O
Reaction #11087
intermediate 28e
Rendimiento 20.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOc1ccc(-c2nnc(-c3cc(Cl)ccc3Cl)n2-c2ccc(OC)cc2)cc1
Reaction #11283
3-(2,5-dichlorophenyl)-4-(4-methoxyphenyl)-5-[4-(octyloxy)phenyl]-4H-1,2,4-triazole
Rendimiento 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)n1ncc(C(=O)NC2C3CC4CC(C3)CC2C4)c1Cl
Reaction #41136
1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)n1ncc(C(=O)NC2C3CC4CC2CC(O)(C4)C3)c1C(F)(F)F
Reaction #41143
1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (5-hydroxy-adamantan-2-yl)-amide
Rendimiento 32.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CNC[C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)OC)c2)c1
Reaction #42354
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CNc1ccc(/C=C/C(=O)N(C)Cc2c(C)[nH]c3ccccc23)cn1
Reaction #46601
title compound
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(-c3cncnc3)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #52119
title compound
Rendimiento 44.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(-c3cncnc3)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1)C(=O)O
Reaction #52120
title compound
Rendimiento 44.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(Cc2ccc(-c3cncnc3)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(S(=O)(=O)N3CCC[C@H]3C(=O)NCCC(N)=O)n21
Reaction #52121
title compound
Rendimiento 10.3%DOI: 10.6084/m9.figshare.5104873.v1
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