子结构搜索

CCOC(=O)Cl

[N-]=[N+]=NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1
Reaction #952
4-(benzyloxycarbonylamidino) benzyl azide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccncc1NC(=O)c1c[nH]c2c1C(=O)CCC2
Reaction #1006
N-(4-methoxy-3-pyridyl)-4-oxo-4,5,6,7-tetrahydro-1H-indole 3-carboxamide
收率 19.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(COc1ccc(C#N)cc1)NC(=O)[C@@H](NC(=O)Oc1ccccc1)C(C)C
Reaction #1025
white powder
收率 14.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCCCC1
Reaction #1172
N-Cbz-piperidine
收率 59.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1282
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@@H]1COC(=O)N1
Reaction #1395
(R)-4-tert-butyl-2-oxazolidinone
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1414
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CCN(C(=O)OCc2ccccc2)N1
Reaction #1426
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1C(=O)[C@@H](CCO)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
Reaction #1900
trans-7-chloro-5-(2-chlorophenyl)-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-ethanol
收率 99.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)OCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl
Reaction #1938
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](OC(=O)OCc3ccccc3)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #2079
3β-benzyloxycarbonyloxy-5-androsten-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)c1cccc(N=C=O)c1
Reaction #2437
title compound
收率 78.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1NS(=O)(=O)c1ccc(CO)cc1
Reaction #2543
title compound
收率 69.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)S(=O)(=O)c1ccc(C(N)=O)cc1
Reaction #2569
title compound
收率 50.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NCc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2603
title compound
收率 72.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2604
title compound
收率 37.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]ccc2sccc12
Reaction #2856
title compound
收率 49.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](/C=C/[C@@H]1C(SCCCCCC(N)=O)=C(OC(=O)CCC)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #3133
(11R,12S,13E,15S)-9-butyryloxy-11,15-bis(tert-butyldimethylsiloxy)-7-thiaprosta-8,13-dienamide
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Cc2ccccc2C1=O
Reaction #3494
2-carbethoxy-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #3710
10,11-Dihydro-10-[4-[(3-methylpropyloxycarbonyl)amino]benzoyl]-5H-pyrrolo[2,1-c][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
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