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CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(SC2CNC(=O)C2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #5160
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2c(C)cc(-c3cn4c(n3)CCCC4)cc2n1Cc1ccc(-c2ccccc2C(=O)OC(C)OC(=O)OC2CCCCC2)cc1
Reaction #320189
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(I)OC(=O)OC1CCCCC1
Reaction #371321
DOI: 10.1039/C8SC04228D
CCCc1nc2c(C)cc(-c3cn4c(n3)CCCC4)cc2n1Cc1ccc(-c2ccccc2C(=O)OC(C)OC(=O)OC2CCCCC2)cc1
Reaction #394953
DOI: 10.1039/C8SC04228D
CC(I)OC(=O)OC1CCCCC1
Reaction #588960
cyclohexyl 1-iodoethyl carbonate
Ausbeute 81.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(I)OC(=O)OC1CCCCC1
Reaction #980103
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(OC(=O)OC(C)I)CC(C)(C)C1
Reaction #980104
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CC(=O)OCC1=C(C(=O)OC(C)OC(=O)OC2CCCCC2)N2C(=O)[C@@H](NC(=O)Cc3csc(N)n3)[C@H]2SC1
Reaction #980106
title compound
Ausbeute 52.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(/C(=N/O)C(=O)N[C@@H]2C(=O)N3C(C(=O)OCCOC(=O)OC4CCCCC4)=C(SCc4cn[nH]c4)CS[C@H]23)cs1
Reaction #1079894
(cyclohexyloxycarbonyloxy)ethyl 7β-[2-(2-aminothiazol-4-yl)-2-(Z)-(hydroxyimino)acetamido]-3-[(pyrazol-4-yl)methylthio]-3-cephem-4-carboxylate
Ausbeute 3.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(SC2CNC(=O)C2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #1117309
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(I)OC(=O)OC1CCCCC1
Reaction #1448226
carbonic acid cyclohexyl ester 1-iodo-ethyl ester
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2scnc2COCCO)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #1886887
title compound
Ausbeute 20969.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2nc(CO)cs2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #1886888
title compound
Ausbeute 89.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2scnc2CO)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #1886895
title compound
Ausbeute 15.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1ncsc1/C=C\SC1=C(C(=O)OC(C)OC(=O)OC2CCCCC2)N2C(=O)[C@H]([C@@H](C)O)[C@H]2[C@H]1C
Reaction #1886903
title compound
Ausbeute 91.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(C)OC(=O)OC2CCCCC2)N2C(=O)C(NC(=O)/C(=N\OC(c3ccccc3)(c3ccccc3)c3ccccc3)c3csc(N)n3)[C@H]2SC1
Reaction #2195028
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Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(OC(=O)OC(C)I)CC(C)(C)C1
Reaction #2242091
DOI: 10.1039/C8SC04228D
CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2scnc2COCCO)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #2333288
title compound
Ausbeute 20969.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2nc(CO)cs2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #2333289
title compound
Ausbeute 89.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2scnc2CO)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #2333296
title compound
Ausbeute 15.9%DOI: 10.6084/m9.figshare.5104873.v1
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