部分構造検索

CCCC(=O)O

CCCC/C=C\CCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5342
4-hydroxy-3-((Z)-1-oxo-9-tetradecenyl)-2(5H)-furanone
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC/C=C\CCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5343
4-hydroxy-3-((Z)-1-oxo-9-hexadecenyl)-2(5H)-furanone
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC#CCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5344
4-hydroxy-3-(1-oxo-9-octadecynyl)-2(5H)-furanone
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5345
4-hydroxy-3-(1-oxooctadecyl)-2(5H)-furanone
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5367
4-hydroxy-3-[1-oxohexadecyl]-2(5H)-furanone
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc2c(c1)NC(=O)[C@H](c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)NC(=O)OC(C)(C)C
Reaction #41850
(S)-2-tert-Butoxycarbonylamino-3-{(S)-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl}-propionic acid methyl ester
収率 56.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc2c(c1)N(C)C(=O)[C@H](c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)NC(=O)OC(C)(C)C
Reaction #41851
(S)-2-tert-Butoxycarbonylamino-3-{(S)-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl}-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC2CCCC(C1)C2N1CC(CO)C(C)(C)C1=O
Reaction #44499
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2(F)CCN(CC3(C(=O)OCc4ccccc4)CCOCC3)CC2)c2ccccc21
Reaction #44889
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(Cc2ccc(N/C(=C3\C(=O)Nc4ccc([N+](=O)[O-])cc43)c3ccccc3)cc2)CC1
Reaction #53155
(Z)-3-{1-[4-(4-ethoxycarbonyl-piperidinomethyl)-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCC1CCCCCCCCCCC1)C1=C(O)COC1=O
Reaction #65578
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCC1CCCCCCCCCCC1)C1=C(O)COC1=O
Reaction #65579
3-(3-Cyclododecyl-1-oxopropyl)-4-hydroxy-2(5H)-furanone
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc2c(c1)NC(=O)[C@H](c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)NC(=O)OC(C)(C)C
Reaction #67335
(S)-2-tert-Butoxycarbonylamino-3-{(S)-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl}-propionic acid methyl ester
収率 56.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc2c(c1)N(C)C(=O)[C@H](c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)NC(=O)OC(C)(C)C
Reaction #67336
(S)-2-tert-Butoxycarbonylamino-3-{(S)-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl}-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1Nc2ccccc2C[C@@H]1C
Reaction #80793
cis-2-methoxycarbonyl-3-methyltetrahydroquinoline
収率 78.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1Nc2ccccc2C[C@@H]1C
Reaction #80794
cis-2-methoxycarbonyl-3-methyltetrahydroquinoline
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCN(c2ccc(Br)cc2)CC1
Reaction #85866
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(Cc2cccc(Nc3nc(Cl)ncc3F)c2)CC1
Reaction #158498
2-chloro-N4-[3-[[4-(ethoxycarbonyl)piperidino]methyl]phenyl]-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](N)Cc1ccc2c(c1)CCCN2
Reaction #162000
#215
収率 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(Cc2cccc(Nc3nc(Cl)ncc3F)c2)CC1
Reaction #163608
2-chloro-N4-[3-[[4-(ethoxycarbonyl)piperidino]methyl]phenyl]-5-fluoro-4-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
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