Teilstruktursuche

C=CCN

CC1=c2cc(Br)ccc2=NC1=O
Reaction #7077
title compound
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1=c2cc(Br)ccc2=NC1=O
Reaction #7078
title compound
Ausbeute 60.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=c2ccccc2=NC1=O
Reaction #7081
title compound
Ausbeute 2.9%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(C(=O)OCc2ccccc2)N(C(=O)OC(C)(C)C)C1
Reaction #7736
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CNN(C(=O)OCc2ccccc2)C1
Reaction #7737
desired product
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=c2ccccc2=NC1=O
Reaction #9422
3-ethyl-indol-2-one
Ausbeute 2.9%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)C(=O)Nc2ccccc21
Reaction #9423
3,3-diethylindol-2-one
Ausbeute 47.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC=C(CO)C1
Reaction #40778
colorless oil
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #42664
title compound
Ausbeute 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #42665
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
C[NH+]1CCC=C(C(=O)O)C1.[Cl-]
Reaction #47744
product
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #48408
title compound
Ausbeute 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #48409
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(CO[Si](C)(C)C(C)(C)C)[C@@H]1[C@@H]([C@@H](C)OC(=O)OCc2ccccc2)C(=O)N1C(Cc1ccc(OC)cc1)Cc1ccc(OC)cc1
Reaction #49995
(3S,4S)-4-(1-t-butyldimethylsilyloxymethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(Cc2ccc(OC)cc2)N2C(=O)[C@H]([C@@H](C)OC(=O)OCc3ccccc3)[C@@H]2C(C)CO[Si](C)(C)C(C)(C)C)cc1
Reaction #49996
(3S,4S)-4-(1-t-butyldimethylsilyloxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di-(p-anisyl)methyl-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(C(=O)OCc2ccccc2)N(C(=O)OC(C)(C)C)C1
Reaction #50944
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CNN(C(=O)OCc2ccccc2)C1
Reaction #50945
desired product
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCCOc1ccccc1CN(CCc1ccc(N)cc1)C(=O)C=Cc1ccccc1.O=C(O)C(=O)O
Reaction #55239
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C=C[C@H](NC(C)=O)C1
Reaction #56068
methyl(+)-cis-4-acetamidocyclopent-2-ene carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=CCCN(C)C1
Reaction #63429
Arecoline
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter