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CN(C)CCOCC=C

CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC)C3)C(C)C(O[Si](C)(C)C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #6398
title compound
Ausbeute 58.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O[Si](C)(C)C(C)(C)C)C2C)C(OC)CC3C)CC1OC
Reaction #6399
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H]1C[C@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)C(=O)N2C(=O)OC[C@@H]2Cc2ccccc2)N(C(=O)OC(C)(C)C)C1
Reaction #49212
(2R,4R)-tert-butyl 2-((1S,2S)-2-(3,5-difluorobenzyl)-3-((S)-4-benzyl-2-oxooxazolidin-3-yl)-1-hydroxy-3-oxopropyl)-4-(allyloxy)pyrrolidine-1-carboxylate
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #49214
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #49215
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cccc(C(=O)O)c1
Reaction #49224
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2CC(O)(c3ccccc3)CN2)c1
Reaction #49236
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CN(C(=O)OC(C)(C)C)CCC1=O
Reaction #71935
title compound
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)COC1CN(C(=O)OC(C)(C)C)CCC1(OC)OC
Reaction #71955
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)COC1CN(C(=O)OC(C)(C)C)CCC1=O
Reaction #71956
title compound
Ausbeute 68.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NCc1ccccc1
Reaction #71957
title compound
Ausbeute 78.7%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC1CN(C(=O)OC(C)(C)C)CCC1=O
Reaction #71961
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/CO[C@H]1C[C@@H](NCc2ccccc2)CCN1C(=O)OC(C)(C)C
Reaction #71962
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1=C(SC2CC(COCCCl)N(C(=O)OCC=C)C2)C(C)C2C(C(C)O)C(=O)N12
Reaction #177857
DOI: 10.1039/C8SC04228D
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1N=[N+]=[N-]
Reaction #185119
DOI: 10.1039/C8SC04228D
C=CCOC1CN(C(=O)OCC)CCC1N
Reaction #192875
DOI: 10.1039/C8SC04228D
C=CCOC(=O)CN1C(=O)C(C(C)O[Si](C)(C)C(C)(C)C)C1SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #196196
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccccc1)C1CC2(c3ccccc3)N(Cc3ccccc3)C1CCC21CC(c2cc(OC(F)(F)F)ccc2OCc2ccccc2)CO1
Reaction #211705
DOI: 10.1039/C8SC04228D
CCCOC[C@H]1CN(C2=Nc3ccccc3Nc3sc(C)cc32)CCN1C
Reaction #218644
title compound
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H]1CCN([C@@H](CCc2ccccc2)C(=O)O)C1=O
Reaction #220118
desired product
DOI: 10.6084/m9.figshare.5104873.v1
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