部分構造検索

1386849

CCn1nc(CC(=O)N2CCCC2)cc1NC(=O)C(F)(F)F
Reaction #90776
product
収率 44.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161951
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methylalanyl-N-[(3R,4S,5S)-3-methoxy-5-methyl-1-oxo-1-(pentafluorophenoxy)heptan-4-yl]-N-methyl-L-valinamide
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161983
#174
収率 92.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)[C@@]1(C)CCCN1C)C(C)C
Reaction #161992
compound #197
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)[C@]1(C)CCCN1C)C(C)C
Reaction #161995
compound #204
収率 125.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCCC(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #201549
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)CCCOC(=O)CCC(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #217780
4
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1c(F)c(F)c(F)c(F)c1F)C1Cc2c(ccc3c2ccn3C(=O)OCC2c3ccccc3-c3ccccc32)N1
Reaction #217782
ester
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(C(=O)NN)c(Nc2ccc(I)cc2F)cc1=O
Reaction #228129
DOI: 10.1039/C8SC04228D
CNC(=O)c1cc(C(=O)Oc2c(F)c(F)c(F)c(F)c2F)c(Nc2ccc(I)cc2C)c(F)c1F
Reaction #251877
DOI: 10.1039/C8SC04228D
CCCCc1nnc(C(=O)Oc2c(F)c(F)c(F)c(F)c2F)cc1-c1ccc(OC2CCCCC2)cc1
Reaction #256497
DOI: 10.1039/C8SC04228D
CCc1ccc(Nc2cc(=O)n(C)cc2C(=O)NCCO)c(F)c1
Reaction #263911
DOI: 10.1039/C8SC04228D
O=C(Oc1c(F)c(F)c(F)c(F)c1F)C(c1c2c(nn1-c1ccc(Cl)cc1)CCC2)C1CCCCC1
Reaction #265617
DOI: 10.1039/C8SC04228D
O=C(NC1CC1)c1ccc(-c2csc(NC(=O)C3COCN3C(=O)OCc3ccccc3)n2)cc1
Reaction #267948
DOI: 10.1039/C8SC04228D
O=C(Cn1cc(Nc2ncnc3cc(OCCCCl)ccc23)cn1)Nc1ccccc1F
Reaction #269634
DOI: 10.1039/C8SC04228D
c1ccc2[nH]cnc2c1
Reaction #310087
compound 3
収率 193.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc(C(=O)Oc2c(F)c(F)c(F)c(F)c2F)cc1C#N
Reaction #310091
6
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OCCCN(CCCC(=O)Oc2c(F)c(F)c(F)c(F)c2F)c2ccc(N=Nc3ccc([N+](=O)[O-])cc3Cl)cc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #401527
DOI: 10.1039/C8SC04228D
COc1cc(CC(=O)Oc2c(F)c(F)c(F)c(F)c2F)ccc1NC(=O)Nc1ccccc1C
Reaction #437527
pentafluorophenyl 3-methoxy-4-[N′-(2-methylphenyl) ureido]phenylacetate
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC[C@@H]1CN(c2ccc(C(=O)Oc3c(F)c(F)c(F)c(F)c3F)c(F)c2)C(=O)O1
Reaction #439056
product
収率 90.1%DOI: 10.6084/m9.figshare.5104873.v1
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