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1268252

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
収率 31.5%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2c3c1O[C@H]1[C@@H](O)CC[C@@]4(O)[C@@H](C2)N(CC2CCC2)CC[C@]314
Reaction #67605
nalbuphine
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCC(=O)[O-]
Reaction #176153
DOI: 10.1039/C8SC04228D
COCOc1ccc2c3c1OC1C(OCc4ccc(C(=O)OC)cc4)CCC4C(C2)N(C)CCC341
Reaction #179827
DOI: 10.1039/C8SC04228D
OC1CCCCC1Oc1ccccc1
Reaction #182385
DOI: 10.1039/C8SC04228D
Oc1ccc2c3c1OC1C(O)CCC4(F)C(C2)N(CC2CCC2)CCC314
Reaction #191878
DOI: 10.1039/C8SC04228D
CCC1C=C(C)C(F)C(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(Oc4ccccc4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #198075
DOI: 10.1039/C8SC04228D
COC(=O)CCCCC(=O)OC1CCC2C3Cc4ccc(OC(C)=O)c5c4C2(CCN3C)C1O5
Reaction #199747
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(Oc4ccc(Cl)cc4)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #221327
DOI: 10.1039/C8SC04228D
CCC(CC)(c1ccc(OC2CCCCC2O)c(C)c1)c1ccc2oc(C(=O)O)cc2c1
Reaction #229548
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NC1CCCCC1Oc1ccc(Br)cc1
Reaction #230259
DOI: 10.1039/C8SC04228D
COc1ccc2c3c1OC1C(O)C(COS(=O)(=O)c4ccc(C)cc4)(COS(=O)(=O)c4ccc(C)cc4)CC4C(C2)N(C)CCC341
Reaction #261679
DOI: 10.1039/C8SC04228D
CC(=O)OC1CCCCC1Oc1ccc(Br)cc1
Reaction #296586
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nc1ccccc1OC1CCCCC1=O
Reaction #300500
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(Oc4ccc(Cl)cc4)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #344871
17-ethyl-1,14-dihydroxy-12-[2' -(3"-(4'"-chlorophenyloxy)-4"-hydroxycyclohexyl)-1'-methylvinyl]-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
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(Oc4ccc(OC)cc4)C(O)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #344872
17-ethyl-1,14-dihydroxy-12-[2'-(4"-(4'"-methoxyphenyloxy)-3"-hydroxycyclohexyl)-1'-methylvinyl]-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
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(Oc4ccc(O)cc4)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #344873
17-ethyl-1,14-dihydroxy-12-[2'-(3"-(4'"-hydroxyphenyloxy)-4"-hydroxycyclohexyl)-1'-methylvinyl] 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
収率 68.4%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(Oc4ccc(O)cc4)C(O)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #344874
17-ethyl-1,14-dihydroxy-12-[2'-(4"-(4'"-hydroxyphenyloxy)-3"-hydroxycyclohexyl)-1'-methylvinyl] 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
収率 64.5%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(Oc4ccc5cc(O)ccc5c4)C(O)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #344875
17-ethyl-1,14-dihydroxy-12-[2'-(4"-(6'"-hydroxynaphth-2-yloxy)-3"-hydroxycyclohexyl)-1'-methylvinyl]-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
収率 48.0%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(Oc4ccc5cc(O)ccc5c4)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #344876
17-ethyl-1,14-dihydroxy-12-[2'-(3"-(6'"-hydroxynaphth-2-yloxy)-4"-hydroxycyclohexyl)-1'-methylvinyl]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
収率 56.2%DOI: 10.6084/m9.figshare.5104873.v1
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