部分構造検索

CCCCO.COCCOC

COCCOCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)C(=O)OC)cc1
Reaction #5822
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccnc(C(=O)N[C@H]2COC[C@H](Cc3cccc4ccccc34)[C@@H](OC(=O)C(C)C)[C@H](C)OC2=O)c1O
Reaction #87240
(3S,6S,7R,8S)-3-(3-hydroxy-4-methoxypicolin-amido)-6-methyl-8-(naphthalen-1-ylmethyl)-4-oxo-1,5-dioxonan-7-yl isobutyrate
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccnc(C(=O)N[C@H]2COC[C@H](Cc3cccc4ccccc34)[C@@H](OC(=O)C(C)C)[C@H](C)OC2=O)c1OCOC(C)=O
Reaction #87241
(3S,6S,7R,8S)-3-(3-(acetoxymethoxy)-4-methoxypicolinamido)-6-methyl-8-(naphthalen-1-ylmethyl)-4-oxo-1,5-dioxonan-7-yl isobutyrate
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccnc(C(=O)N[C@H]2COC[C@H](Cc3cccc4ccccc34)[C@@H](OC(=O)C(C)C)[C@H](C)OC2=O)c1OC(C)=O
Reaction #87242
(3S,6S,7R,8S)-3-(3-acetoxy-4-methoxypicolinamido)-6-methyl-8-(naphthalen-1-ylmethyl)-4-oxo-1,5-dioxonan-7-yl isobutyrate
収率 93.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1OC(COCc2ccc(OC)cc2)(COCc2ccc(OC)cc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #87465
product
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1OC(COCc2ccc(OC)cc2)(COCc2ccc(OC)cc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #87485
product
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1[C@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90570
307
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OCCO)cc3)cn(CC(=O)OCC)c12
Reaction #155348
ethyl{5-fluoro-3-[4-(2-hydroxyethoxy)phenyl]-4-oxo-8-propoxy-4H-quinolin-1-yl}acetate
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=S)N[C@@]1(c2cc(Br)ccc2F)CO[C@@H](COCc2ccccc2)C[C@H]1CO)c1ccccc1
Reaction #155595
product
収率 63.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3cc(Br)ccc3F)CO[C@@H](COCc3ccccc3)C[C@H]2CS1)c1ccccc1
Reaction #155596
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC[C@H]1O[C@H](O[C@@H]2[C@H](OC(=O)c3ccccc3)[C@@H](O[C@@H]3[C@H](OC(=O)c4ccccc4)[C@@H](OCc4ccccc4)O[C@H](COC(=O)c4ccccc4)[C@H]3OC(=O)c3ccccc3)O[C@H](COC(=O)c3ccccc3)[C@H]2OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)c1ccccc1
Reaction #162021
trisaccharide
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@H]1O[C@H](CO)[C@@H](OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)c1ccccc1
Reaction #162036
white solid
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(C)(C)OCC1CCCC(O)C1
Reaction #180348
DOI: 10.1039/C8SC04228D
CC(=O)OC1OC(C)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #181485
DOI: 10.1039/C8SC04228D
COCOCCc1ccc(Cc2ccc(OC)cc2OC2OC(COC(C)=O)C(OC(C)=O)C(OC(C)=O)C2OC(C)=O)cc1
Reaction #182418
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1cccc(OCC(=O)OC(C)(C)C)c1)OC
Reaction #188242
DOI: 10.1039/C8SC04228D
COC1(c2ccc(Cl)c(Cc3ccc(OCCOC4CC4)cc3)c2)OC(C=O)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #189706
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O
Reaction #191410
DOI: 10.1039/C8SC04228D
COC1(c2ccc(Cl)c(Cc3ccc(OC(F)(F)F)cc3)c2)OC(CO)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #191865
DOI: 10.1039/C8SC04228D
CCc1oc(-c2ccc(C(F)(F)F)cc2)nc1COCC1CCCC(COC(C)(C)C(=O)OC(C)(C)C)C1
Reaction #196328
DOI: 10.1039/C8SC04228D
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