Busqueda de Subestructura

1267229

C=COc1cccc2c(OC=C)cccc12
Reaction #43967
1,5-bis(vinyloxy)naphthalene
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C
Reaction #74993
rifampicin
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C
Reaction #74994
rifampicin
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C
Reaction #74995
rifampicin
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc2c(O)cccc2c1O
Reaction #157187
1,5-Dihydroxy-naphthalene-2-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1ccc2c(OCc3ccccc3)cccc2c1OCc1ccccc1
Reaction #157188
1,5-Bis-benzyloxy-naphthalene-2-carboxylic Acid Benzyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc2c(OCc3ccccc3)cccc2c1OCc1ccccc1
Reaction #157190
creamy white solid
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1c1ncc(-c2ccc(-c3cccc4c(OS(=O)(=O)C(F)(F)F)cccc34)cc2)[nH]1
Reaction #159020
2-{5-[4-(5-Trifluoromethanesulfonyloxy-naphthalen-1-yl)-phenyl]-1H-imidazol-2-yl}-pyrrolidine-1-carboxylic acid tert-butyl ester
Rendimiento 80.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1c1ncc(-c2ccc(-c3cccc4c(OS(=O)(=O)C(F)(F)F)cccc34)cc2)[nH]1
Reaction #166971
2-{5-[4-(5-Trifluoromethanesulfonyloxy-naphthalen-1-yl)-phenyl]-1H-imidazol-2-yl}-pyrrolidine-1-carboxylic acid tert-butyl ester
Rendimiento 80.3%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc2c(Oc3ccccc3)cccc12
Reaction #177177
DOI: 10.1039/C8SC04228D
COc1cc(COC2CN(C(=O)OC(C)(C)C)CCC2c2ccc(OCCCOCc3cccs3)cc2)cc2c(OC)cccc12
Reaction #185248
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cccc2c(O)cccc12
Reaction #189005
DOI: 10.1039/C8SC04228D
CCOC(=O)COc1cccc2c(O)cccc12
Reaction #209383
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(C(=O)OCC)c(-c2ccc3c(c2)OCO3)c2c3c(ccc2c1OC)OCO3
Reaction #233026
DOI: 10.1039/C8SC04228D
COc1cc(COC2CN(C(=O)OC(C)(C)C)CCC2c2ccc(OCCCSCc3ccccc3)cc2)cc2c(OC)cccc12
Reaction #241510
DOI: 10.1039/C8SC04228D
COc1cc(CO)cc2c(OC)cccc12
Reaction #255326
DOI: 10.1039/C8SC04228D
COc1ccc(OC)c2c(OC)c(C(CCC(C)C)OC(C)=O)cc(OC)c12
Reaction #298006
DOI: 10.1039/C8SC04228D
COCCCOc1cc(COC2CN(C(=O)OC(C)(C)C)CCC2c2ccc(OCCCOCc3cccs3)cc2)cc2c(OC)cccc12
Reaction #300372
DOI: 10.1039/C8SC04228D
NNC(=O)c1ccncc1
Reaction #307520
isoniazid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #313433
crude brown solid
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
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