子结构搜索

3806

CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@](C)(O)C[C@@H](C)CN(C)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #52549
Azithromycin monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Cc2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)nn1
Reaction #74471
title compound
收率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1nnc(Cc2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)s1
Reaction #74474
title compound
收率 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nnc(Cc2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)s1
Reaction #74475
title compound
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc(C3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)nn1
Reaction #74485
3-(2-Chloro-5-((3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyl)-6-ethoxypyridazine
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cnc(Cc2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)nn1
Reaction #74492
title compound
收率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1c(-c2ccc(OC3CCOCC3)cc2)nn2c1NCCC2c1ccccc1N
Reaction #92565
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC1OC(c2ccc(Cl)c(Cc3ccc(-c4ccc(C=O)c(F)c4)s3)c2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #173799
DOI: 10.1039/C8SC04228D
COC1(c2cnc(Sc3ccc4c(c3)CCC(=O)N4C)s2)CCOC(C)(C)C1
Reaction #174591
DOI: 10.1039/C8SC04228D
COc1nc(N)ncc1-c1nc(OC2CCOCC2)cc(N2CCOCC2)n1
Reaction #179425
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(Oc2cccc3occ(CCc4ccc(NS(C)(=O)=O)cc4)c23)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #179459
DOI: 10.1039/C8SC04228D
Clc1nnc(Cc2cc(C3OC(COCc4ccccc4)C(OCc4ccccc4)C(OCc4ccccc4)C3OCc3ccccc3)ccc2Cl)s1
Reaction #187054
DOI: 10.1039/C8SC04228D
COC1(c2cccc(Sc3ccc(N(C)S(C)(=O)=O)cn3)c2)CCOCC1
Reaction #199429
DOI: 10.1039/C8SC04228D
—
Reaction #217188
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(CCCC(C)C1CCC2C3CCC4CCCCC4(C)C3CCC12C)COC1OC(COC(=O)C(C)(C)C)C(OCc2ccccc2)C(O)C1OCc1ccccc1
Reaction #223180
DOI: 10.1039/C8SC04228D
OC1(c2cc(Cc3cc4ccccc4s3)cc3ccccc23)OC(COCc2ccccc2)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #241533
DOI: 10.1039/C8SC04228D
C=CC1(COS(=O)(=O)c2ccc(C)cc2)OC(OC2C(COCc3ccccc3)OC(OC)C(OCc3ccccc3)C2OCc2ccccc2)C(OC(C)=O)C(OC)C1O
Reaction #241911
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(c2ccc(C)c(Cc3ccc(-c4cncnc4)s3)c2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #246157
DOI: 10.1039/C8SC04228D
COC1(c2cc(F)cc(Sc3ccc4c(c3)CCC(=S)N4C)c2)CCOCC1
Reaction #260734
DOI: 10.1039/C8SC04228D
CC(=O)OCC1OC(n2cc(C(=O)c3ccc(I)cc3)c3c(Cl)cccc32)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #275467
DOI: 10.1039/C8SC04228D
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