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COc1ccc2c(c1)C(=O)N1C=C(OS(=O)(=O)C(F)(F)F)C(OCCCOC3C(OS(=O)(=O)C(F)(F)F)=CN4C(=O)c5cc(OC)ccc5N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]34)[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)N2C(=O)OCC(Cl)(Cl)Cl
Reaction #47141
triflate
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccccc1C1(OCCCOC2(c3ccccc3C#C)C=CN3C(=O)c4cc(OC)ccc4N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]32)C=CN2C(=O)c3cc(OC)ccc3N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]21
Reaction #47142
17
Ausbeute 92.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(C)C)C(C)C
Reaction #64774
N,N-diisopropylethylamine
Ausbeute 104.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(=O)N(C)C)C3)[C@H](C)[C@H]12
Reaction #165861
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1=C(Sc2nc(C3=CC(C)N(C(=O)OCC=C)CC3)cs2)C(C)C2C(C(C)O[Si](C)(C)C)C(=O)N12
Reaction #199803
DOI: 10.1039/C8SC04228D
Cc1ccccc1S(=O)(=O)OC1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #334667
benzyl 3-toluenesulfonyloxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1S(=O)(=O)OC1=C(C(=O)OCc2ccccc2)N2C(=O)C(C(O)C(F)(F)F)C2C1
Reaction #334668
BENZYL 6-(2,2,2-TRIFLUORO-1-HYDROXYETHYL)-3-TOLUENESULFONYLOXY-1-AZABICYCLO[3.2.0]HEPT-2-EN-7-ONE-2-CARBOXYLATE
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)C1=C(N2CCOCC2)CC2C(C(O)C(F)(F)F)C(=O)N12
Reaction #334671
benzyl 6-(2,2,2-trifluoro-1-hydroxyethyl)-3-morpholino-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC2=C(C(=O)OCc3ccccc3)N3C(=O)CC3C2)cc1
Reaction #334675
benzyl 3-(p-toluenesulfonyloxy)-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #334681
benzyl 3 -methoxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
Ausbeute 20.5%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC1=C(C(=O)OCc2ccccc2)N2C(=O)C[C@H]2C1
Reaction #416845
benzyl-2-azido-carbapen-2-em-3-carboxylate
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC1=C(C(=O)OCc2ccccc2)N2C(=O)C[C@H]2C1
Reaction #416846
benzyl 2-azidocarbapen-2-em-3-carboxylate
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@H]3C[C@@H](C(=O)N4CC(NC=N)C4)N(C)C3)[C@H](C)[C@H]12
Reaction #449274
title compound
Ausbeute 7.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N4CC(N(C)C)C4)N(C(=O)OCc4ccc([N+](=O)[O-])cc4)C3)[C@H](C)[C@H]12
Reaction #449276
title compound
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(=O)NC4CNC4)C3)[C@H](C)[C@H]12
Reaction #449281
title compound
Ausbeute 14.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1S(=O)(=O)OC1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #458460
benzyl 3-toluenesulfonyloxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1S(=O)(=O)OC1=C(C(=O)OCc2ccccc2)N2C(=O)C(C(O)C(F)(F)F)C2C1
Reaction #458461
Benzyl 6-(2,2,2-trifluoro-1-hydroxyethyl)-3-toluenesulfonyloxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)C1=C(N2CCOCC2)CC2C(C(O)C(F)(F)F)C(=O)N12
Reaction #458464
benzyl 6-(2,2,2-trifluoro-1-hydroxyethyl)-3-morpholino-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC2=C(C(=O)OCc3ccccc3)N3C(=O)CC3C2)cc1
Reaction #458468
benzyl 3-(p-toluenesulfonyloxy)-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #458474
benzyl 3 -methoxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
Ausbeute 20.5%DOI: 10.6084/m9.figshare.5104873.v1
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