بحث البنية الفرعية

328790

CCCCC(=CC(=O)OCC)OS(=O)(=O)C(F)(F)F
Reaction #65256
ethyl 3-trifluoromethanesulfonyloxy-2-heptenoate
DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3cccnc3CSCCN(C)C(=O)OC(C)(C)C)CCC12)c1nc(N)sc1Cl
Reaction #194813
DOI: 10.1039/C8SC04228D
Nc1nc(C(=NOC(c2ccccc2)(c2ccccc2)c2ccccc2)C(=O)NC2C(=O)N3C(C(=O)OC(c4ccccc4)c4ccccc4)=C(Sc4nnc(N)s4)CCC23)ns1
Reaction #222290
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C=C(CCCCCCc1ccc2c(n1)NCCC2)c1cc2ccccc2s1
Reaction #246740
DOI: 10.1039/C8SC04228D
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3nnc(N)s3)CCC12)c1nsc(N)n1
Reaction #263423
DOI: 10.1039/C8SC04228D
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(OS(=O)(=O)C(F)(F)F)CCC12)c1nsc(N)n1
Reaction #268716
DOI: 10.1039/C8SC04228D
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3cccnc3CNC(=O)OC(C)(C)C)CCC12)c1nc(N)sc1Cl
Reaction #281031
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C=C(CCCCCCc1ccc2c(n1)NCCC2)c1ccccc1
Reaction #293365
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C=C(CCCCCCc1ccc2c(n1)NCCC2)c1ccccc1
Reaction #466459
29-7a
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC=CC(=O)OC(C)(C)C
Reaction #466461
29-7b
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C=C(CCCCCCc1ccc2c(n1)NCCC2)c1nc2ccccc2s1
Reaction #466463
29-7c
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(SC(C)=O)CCC2(C1)OCCO2
Reaction #633518
title compound
المردود 45.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCc3ccccc3)=C(OS(=O)(=O)C(F)(F)F)CC[C@H]12
Reaction #707561
benzyl 7-phenoxyacetylamino-3-trifluoromethylsulfonyloxy-1-carba-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cccs1)N[C@@H]1C(=O)N2C(C(=O)O)=C(OS(=O)(=O)C(F)(F)F)CC[C@H]12
Reaction #707564
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(OS(=O)(=O)C(F)(F)F)CC[C@H]12)c1csc(N)n1
Reaction #707565
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCc3ccccc3)=C(OS(=O)(=O)C(F)(F)F)CC[C@H]12
Reaction #739987
benzyl 7-phenoxyacetylamino-3-trifluoromethylsulfonyloxy-1-carba-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cccs1)N[C@@H]1C(=O)N2C(C(=O)O)=C(OS(=O)(=O)C(F)(F)F)CC[C@H]12
Reaction #739990
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(OS(=O)(=O)C(F)(F)F)CC[C@H]12)c1csc(N)n1
Reaction #739991
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCSCc1ncccc1SC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)C(=NOC(c3ccccc3)(c3ccccc3)c3ccccc3)c3nsc(N)n3)C2CC1
Reaction #906414
DOI: 10.1039/C8SC04228D
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3cccnc3CSC3CCN(C(=O)OC(C)(C)C)C3)CCC12)c1nc(N)sc1Cl
Reaction #920277
DOI: 10.1039/C8SC04228D
الصفحة 1التالي