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446524

COC(=O)c1sc(C#CC(C)(C)C)cc1N(C(=O)[C@H]1CC[C@H](C)CC1)[C@@H](C)CCNC(=O)OC1COC2OCCC12
Reaction #67574
5-(3,3-Dimethyl-but-1-ynyl)-3-[[3-(hexahydro-furo[2,3-b]furan-3-yloxycarbonylamino)-1-(S)-methyl-propyl]-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(C#CC(C)(C)C)cc1N(C(=O)[C@H]1CC[C@H](C)CC1)C1CCC(NC(=O)OC2COC3OCCC23)CC1
Reaction #67575
5-(3,3-Dimethyl-but-ynyl)-3-[[4-(hexahydro-furo[2,3-b]furan-3-yloxycarbonylamino)-cyclohexyl]-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)Oc1ccc([N+](=O)[O-])cc1
Reaction #71558
butyl 4-nitrophenyl carbonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)N=C(N)c1ccc(OCCCC2CCN(CCCOc3ccc(C(N)=NC(=O)OCCCC)cc3)CC2)cc1
Reaction #71560
4-{3-[4-(3-{4-[amino(butoxycarbonylimino)methyl]phenoxy}propyl)-1-piperidinyl]propoxy}-N′-(butoxycarbonyl)benzamidine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)cn2C1CCC(OC(=O)Oc2ccc([N+](=O)[O-])cc2)C1
Reaction #79793
3-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopentyl (4-nitrophenyl) carbonate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)cn2C1CCC(OC(=O)NCCN2CCOCC2)C1
Reaction #79794
3-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopentyl N-(2-morpholinoethyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCCCOC(=O)N1CCC2(CCCC2)CC1)OC1CCN(C(=O)Oc2ccc(Oc3ccccc3)cc2)CC1
Reaction #177871
DOI: 10.1039/C8SC04228D
CCC1CC(OC(=O)Oc2ccc([N+](=O)[O-])cc2)CC1c1nnc2cnc3c(ccn3S(=O)(=O)c3ccc(C)cc3)n12
Reaction #178312
DOI: 10.1039/C8SC04228D
CC(C)CN(CC(O)C(Cc1ccc(OCc2ccccc2)cc1)NC(=O)OC1COC2OCCCC12)S(=O)(=O)c1ccc2c(c1)OCO2
Reaction #191339
DOI: 10.1039/C8SC04228D
COC(=O)C(CCCc1ccc(OCc2nc(-c3ccco3)oc2C)c(OC)c1)OC(N)=O
Reaction #244243
DOI: 10.1039/C8SC04228D
COC(=O)c1sc(C#CC(C)(C)C)cc1N(C(=O)C1CCC(C)CC1)C(C)CCNC(=O)OC1COC2OCCC12
Reaction #245001
DOI: 10.1039/C8SC04228D
O=C(NCCCCCCOC(=O)N1CCC(O)CC1)Oc1ccc(Oc2ccccc2)cc1
Reaction #260815
DOI: 10.1039/C8SC04228D
COC(=O)c1sc(C#CC(C)(C)C)cc1N(C(=O)C1CCC(C)CC1)C1CCC(NC(=O)OC2COC3OCCC23)CC1
Reaction #263707
DOI: 10.1039/C8SC04228D
CC12CCC(OC(=O)OCCN3CCCC3)CC1CCC1C2CCC2(C)C(c3ccc(=O)oc3)CCC12O
Reaction #266004
DOI: 10.1039/C8SC04228D
Cc1cn(C2CC(O[Si](C)(C)C(C)(C)C)C(COC(=O)Oc3ccc([N+](=O)[O-])cc3)O2)c(=O)[nH]c1=O
Reaction #287505
DOI: 10.1039/C8SC04228D
Cc1nc2ccccc2n1C1CC2CCC(C1)N2CCC1(c2ccccc2)CCN(C(=O)OC2COC3OCCC23)CC1
Reaction #291302
DOI: 10.1039/C8SC04228D
O=C(OCCCCC(CO[N+](=O)[O-])O[N+](=O)[O-])Oc1ccc([N+](=O)[O-])cc1
Reaction #294157
DOI: 10.1039/C8SC04228D
O=C(NCCCCCCOC(=O)N1CCC(O)CC1)Oc1ccc(Oc2ccccc2)cc1
Reaction #347518
yellow oil
収率 158.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCCC(C)C1CCC2C3CCC4CC(OC(=O)Oc5ccc([N+](=O)[O-])cc5)CCC4(C)C3CCC12C
Reaction #370307
DOI: 10.1039/C8SC04228D
O=C(OC1CN2CCC1CC2)N1CCc2ccccc2C1c1ccccc1
Reaction #376823
DOI: 10.1039/C8SC04228D
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