部分構造検索

1853

O=C(OCc1ccccc1)N1CCC(N2C(=O)c3ccccc3C2=O)CC1
Reaction #1173
1-benzyloxycarbonyl-4-phthalimidylpiperidine
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC(=O)C2CCOCC2)cc1OC
Reaction #1770
methyl 4-(4-tetra-hydropyranoyloxy)-2-methoxy-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC(=O)[C@@H]2CCCC[C@@H]2c2ccccc2)cc1OC
Reaction #1773
methyl 4-(cis-2-phenyl-1-cyclohexanoyloxy)-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC(=O)C2CCOc3ccccc32)cc1OC
Reaction #1778
methyl 4-(4-chromanoyloxy)-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC(=O)[C@H]2CC[C@@H](NC(=O)OC(C)(C)C)CC2)cc1OC
Reaction #1790
methyl 4-[N-Boc-cis-1-amino-4-cyclohexanoyloxy]-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC(=O)c2cc(=S(=O)=O)cco2)cc1OC
Reaction #1793
methyl 4-[4-sulfonylpyranoyloxy]-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(F)nc(F)c(F)c1OC(C)(C)C
Reaction #1971
title product
収率 85.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](C)Oc1ccccc1C=Cc1cc2ccccc2n1C
Reaction #2244
(S)-2-{2[2-(1-methoxycarbonylethoxy)phenyl]vinyl}-1-methylindole
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(OC2CCN(c3ccncc3)CC2)cc1
Reaction #2322
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(COc1ccc(N2CCN(c3ccncc3)CC2)cc1)CC(=O)OC
Reaction #2341
methyl 4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenoxy]-3-vinylbutyrate
収率 19.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(CN2C(=O)CCC2=O)cc1
Reaction #2570
title compound
収率 66.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2nnn[nH]2)cc1Br
Reaction #3074
5-(3'-bromo-4'-methylphenyl)tetrazole
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1ccccc1SSc1ccccc1C(=O)c1ccccc1
Reaction #3842
title compound
収率 50.7%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #5043
compound
収率 71.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SC1CNC(=O)C1
Reaction #5215
4-acetylthio-2-pyrrolidinone
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)(CN=[N+]=[N-])NC(=O)OCc1ccccc1
Reaction #5652
1-Azido-2-(benyloxycarbonylamino)-2-methylbutane
DOI: 10.6084/m9.figshare.5104873.v1
CN(CC=Cc1ccc(Cl)cc1)CCN(CCN1CCCCC1)S(=O)(=O)c1cccc2cnccc12
Reaction #5841
title compound
収率 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CO[C@@H](COn1cnc2c(OC)nc(N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)nc21)CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)OCC
Reaction #6361
(S)-2-[bis-(t-butoxycarbonyl)amino]-9-[3-(t-butyldiphenylsilyloxy)-2-(diethoxyphosphorylmethoxy)propoxy]-6-methoxypurine
収率 32.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CO[C@@H](COCc1ccccc1)COn1cnc2c(OC)nc(N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)nc21)OCC
Reaction #6365
(S)-2-[bis-(t-butoxycarbonyl)amino]-9-[3-benzyloxy-2-(diethoxyphosphorylmethoxy)propoxy]-6-methoxypurine
収率 88.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1cn2c(n1)C(CCSC(c1ccccc1)(c1ccccc1)c1ccccc1)N(C(=O)OC(C)(C)C)CC2
Reaction #6869
foam
収率 111.0%DOI: 10.6084/m9.figshare.5104873.v1
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