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O=S1CCCC1

O=C(c1ccc(Cl)cc1)c1ccc(C2CCCS2(=O)=O)cc1
Reaction #2197
desired product
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
Reaction #41843
5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-2H-indol-2-one
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
Reaction #41845
5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-2H-indol-2-one
Выход 74.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)Cl)cc1
Reaction #43888
white solid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)c2c1cccc2S(=O)(=O)Cl
Reaction #43889
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(-c2ncco2)cc1
Reaction #44750
4-(2-oxazolyl)phenyl acetate
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(C(F)(F)F)cc1Oc1cc(Oc2cc(C(F)(F)F)nn2C)nc(Oc2cc(C(F)(F)F)nn2C)c1
Reaction #51597
colorless crystals
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(F)(F)C(F)F)nc(Oc2cc(C(F)(F)F)nn2C)c1
Reaction #51599
title compound
Выход 99.2%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)OCCN(CCC#N)c1ccccc1
Reaction #54194
N-(2-cyanoethyl)-N-[2-(N-ethylcarbamoyloxy)ethyl]aniline
DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)OCCN(CCC#N)c1ccccc1
Reaction #54195
N-(2-cyanoethyl)-N-[2-(N-propylcarbamoyloxy)ethyl]aniline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(c1cnc(C(C)(C)C)nc1F)C(C)C
Reaction #62875
ethyl (RS)-2-[2-(2-methylprop-2-yl)-4-fluoropyrimidin-5-yl]-3-methylbutyrate
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2c(sc3ncnc(Cl)c23)C1
Reaction #66791
title compound
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2c(sc3ncc(C#N)c(Cl)c23)C1
Reaction #66818
title compound
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCc2c(sc3ncnc(Cl)c23)C1
Reaction #66839
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc([S+]2CCCC2)c2ccccc12.[Cl-]
Reaction #70120
4-hydroxynaphthyl-1-tetrahydrothiophenium chloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)cc2c1c(C)cn2C(C)C
Reaction #70783
methyl 6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylate
Выход 89.2%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)n1cc(C)c2c(C(=O)OC)cc(Br)cc21
Reaction #70787
methyl 6-bromo-1-sec-butyl-3-methyl-1H-indole-4-carboxylate
Выход 54.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C(=O)Nc1cccnc1N2
Reaction #72516
8-methyl-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one
Выход 70.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1c(Oc2nc(OC)cc(OC)n2)ccc2[nH]c(C)c([N+](=O)[O-])c12
Reaction #80290
desired compound
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSC2CC(CO)S(=O)(=O)C2)cc1
Reaction #83077
desired product
DOI: 10.6084/m9.figshare.5104873.v1
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