An 17 Reaktionen beteiligt

10063

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.v1uspto-grants-1993_09

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.v1uspto-grants-1997_01

Reaction #371321

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction #394953

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction #588960

cyclohexyl 1-iodoethyl carbonate

Ausbeute 81.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08

Reaction #980103

title compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_06

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.v1uspto-grants-1992_06

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.v1uspto-grants-2002_10

Reaction #1117309

title compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_04

Reaction #1448226

carbonic acid cyclohexyl ester 1-iodo-ethyl ester

Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02

$CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2scnc2COCCO)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12$

Reaction #1886887

title compound

Ausbeute 20969.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01

$CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2nc(CO)cs2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12$

Reaction #1886888

title compound

Ausbeute 89.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01

$CC(=O)OCc1ncsc1/C=C\SC1=C(C(=O)OC(C)OC(=O)OC2CCCCC2)N2C(=O)[C@H]([C@@H](C)O)[C@H]2[C@H]1C$

Reaction #1886903

title compound

Ausbeute 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01

$C/C=C\C1=C(C(=O)OC(C)OC(=O)OC2CCCCC2)N2C(=O)C(NC(=O)/C(=N\OC(c3ccccc3)(c3ccccc3)c3ccccc3)c3csc(N)n3)[C@H]2SC1$

Reaction #2195028

product

Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_06

$CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2scnc2COCCO)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12$

Reaction #2333288

title compound

Ausbeute 20969.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_03

$CC(OC(=O)OC1CCCCC1)OC(=O)C1=C(S/C=C\c2nc(CO)cs2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12$

Reaction #2333289

title compound

Ausbeute 89.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_03

$CC(=O)OCc1ncsc1/C=C\SC1=C(C(=O)OC(C)OC(=O)OC2CCCCC2)N2C(=O)[C@H]([C@@H](C)O)[C@H]2[C@H]1C$

Reaction #2333304

title compound

Ausbeute 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_03