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81254

CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1N
Reaction #47828
titled compound
収率 82.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1N
Reaction #47830
titled compound
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1NC(C)=O
Reaction #47837
titled compound
収率 71.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1NC(=O)CC
Reaction #47838
titled compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1NC(C)=O
Reaction #47839
titled compound
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC1C(C(=O)OCC)=C(c2ccccc2)c2ccc(OC)cc21
Reaction #47841
titled compound
収率 75.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1N1CCOCC1
Reaction #47842
titled compound
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1NCc1ccccc1
Reaction #47843
titled compound
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1NC1CCCCC1
Reaction #47844
titled compound
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC1(c2ccc(Br)cc2)c2ccccc2-c2nccn21
Reaction #74444
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1(c2ccc(Br)cc2)c2ccccc2-c2[nH+]ccn21.O=C([O-])C(F)(F)F
Reaction #74445
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1(c2ccc(Br)cc2)c2ccccc2-c2nccn21)N1CCCC1
Reaction #74446
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(c2ccc(Br)cc2)c2ccccc2-c2nccn21
Reaction #74447
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCc2ccccc2C1N.Cl
Reaction #92697
methyl rac-(1S,2S)-1-amino-1,2,3,4-tetrahydronaphthalene-2-carboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1Cc2ccccc2C1N.Cl
Reaction #92698
methyl rac-(1R,2R)-1-aminoindane-2-carboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C[C@@H](C(=O)OC(C)(C)C)[C@@H]2N(Cc1ccccc1)[C@H](C)c1ccccc1
Reaction #92701
tert-butyl (1S,2R)-1-{benzyl[(1R)-1-phenylethyl]amino}-5-methylindane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1Cc2cccc(F)c2[C@H]1N[S@@](=O)C(C)(C)C
Reaction #92705
tert-butyl (1S,2R)-1-{[(S)-tert-butylsulfinyl]amino}-7-fluoroindane-2-carboxylate
収率 34.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2c1[C@@H](N)[C@H](C(=O)OC(C)(C)C)C2
Reaction #92706
tert-butyl (1S,2R)-1-amino-7-methylindane-2-carboxylate
収率 89.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1Cc2cccc(F)c2[C@H]1N
Reaction #92707
methyl (1S,2R)-1-amino-7-fluoroindane-2-carboxylate
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C[C@@H](C(=O)O)[C@@H]2NC(=O)c1c(C)nc2c(OCC3CCCCC3)cccn12
Reaction #92768
(1S,2R)-1-({[8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)-5-methylindane-2-carboxylic acid
収率 87.1%DOI: 10.6084/m9.figshare.5104873.v1
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