子结构搜索

98099

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Reaction #2243
oil
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OCc4cccc(CO[Si](C)(C)C(C)(C)C)c4)C(OC)C3)C(C)C(O[Si](C)(C)C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #6392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CC1OC
Reaction #6393
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #6394
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6395
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(Oc4cccc(C=O)c4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6401
title compound
收率 31.5%DOI: 10.6084/m9.figshare.5104873.v1
ClCCl.N
Reaction #61996
ammonia DCM
收率 2.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)N1CCCC2CCCCC21
Reaction #67493
ethyl 3-(octahydroquinolin-1-yl)-3-oxopropionate
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OC(=O)CCC(=O)O)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #83379
17-allyl-12-[2-[4-(3-carboxypropionyloxy)-3-methoxycyclohexyl]-1-methylvinyl]-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O[Si](c4ccccc4)(c4ccccc4)C(C)(C)C)C(OC)C3)C(C)C=CC1=O)C(C)CC2OC
Reaction #83381
17-allyl-12-[2-(4-tert-butyl-diphenylsilyloxy-3-methoxycyclohexyl)-1-methylvinyl]-1-hydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacosa-14,18-diene-2,3,10,16-tetraone
收率 72.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OC(=O)NCCCC(=O)OCC[Si](C)(C)C)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #83383
17-allyl-12-[2-[3-methoxy-4-{3-(2-trimethylsilylethoxycarbonyl)propylcarbamoyloxy}cyclohexyl]-1-methylvinyl]-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)N1CCCC2CCCCC21
Reaction #155510
yellow oil
收率 78.9%DOI: 10.6084/m9.figshare.5104873.v1
COCCC(=O)N1CCC(F)(F)CC1CNc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162089
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3C(O[SiH](C)C)CCCC3C(=O)OC(C(C)=CC3CCC(O)(C(C(C)=O)c4ccccc4)C(OC)C3)C(C)C(C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #175097
DOI: 10.1039/C8SC04228D
O=C1CCCC2CC=CC(c3cc(F)c(F)c(F)c3)N12
Reaction #182717
DOI: 10.1039/C8SC04228D
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1N=[N+]=[N-]
Reaction #185119
DOI: 10.1039/C8SC04228D
Cc1nc2ccc3c(c2o1)OC(CN1C2CCC1CC(O)(c1ccccc1)C2)CO3
Reaction #185435
DOI: 10.1039/C8SC04228D
Clc1ccc(OCc2nc3c(OCCCN4CCCCC4CCN4CCCCC4)cccc3n2CCCC2CCNCC2)cc1
Reaction #186557
DOI: 10.1039/C8SC04228D
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1NC(=O)C1CC1
Reaction #190231
DOI: 10.1039/C8SC04228D
C=CCC1(C)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CC)CC(C)(C)O)C1=O
Reaction #201190
DOI: 10.1039/C8SC04228D
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