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215680

C=C(C)c1c(F)cnc2cc(F)c(OC)nc12
Reaction #43412
3,7-Difluoro-8-(1-methylethenyl)-2-(methyloxy)-1,5-naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc2c(nn1)OCCC2
Reaction #43428
product
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc2c(nn1)SCCO2
Reaction #43432
solid
Ausbeute 71.2%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc2c(nn1)OCC2
Reaction #43457
3-Ethenyl-5,6-dihydrofuro[2,3-c]pyridazine
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc2c(c1)C(=O)NCC2
Reaction #43633
product
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49495
4-vinyl-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(-c2cc3cc(CN4CCN(CCO[Si](C)(C)C(C)(C)C)CC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49499
4-vinyl-7-{1-(tert-butoxycarbonyl)-5-[4-(2-tert-butyldimethylsilyloxyethyl)pyperazin-1-ylmethyl]indol-2-yl}isoindolinone
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c(c1Cl)CNC2=O
Reaction #49588
4-chloro-5-vinyl-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ncnc(Nc2ccc(C(F)(F)F)cc2)n1
Reaction #164658
N-(4-(trifluoromethyl)phenyl)-4-vinyl-1,3,5-triazin-2-amine
Ausbeute 16.5%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cnn(C)c1-c1csc(C(=O)OC)c1
Reaction #199063
DOI: 10.1039/C8SC04228D
C=COc1cc([C@@](Cc2ccccc2)(N[S@@](=O)C(C)(C)C)c2cc(F)cc(OC(F)(F)C(F)F)c2)ccc1F
Reaction #326038
(S)—N—((R)-1-(4-fluoro-3-(vinyloxy)phenyl)-1-(3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl)-2-phenylethyl)-2-methylpropane-2-sulfinamide
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1nc(C(=O)OCCCC)c(O)c2ccc(Oc3ccccc3)cc12
Reaction #337677
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1nc(OCC)n(Cc2ccc(-c3ccccc3C(=O)OC(C)(C)C)cc2F)c1C=O
Reaction #428572
intermediate ( 15b )
Ausbeute 99.8%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(C(C)=O)cn1
Reaction #471012
1-(6-Vinylpyridin-3-yl)ethanone
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1nc(OCC)n(Cc2ccc(-c3ccccc3C(=O)OC(C)(C)C)cc2F)c1C=O
Reaction #562852
compound A
Ausbeute 209.8%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1nc(OCCC)n(Cc2ccc(-c3ccccc3C(=O)OC(C)(C)C)cc2F)c1C=NO
Reaction #562860
compound C
Ausbeute 88.8%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1c(F)c(Cl)cc(C(C)Nc2ncnc3c2ncn3C2CCCCO2)c1OC
Reaction #598187
desired compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1c(C)c(Cl)cc(C(C)NC(=O)OC(C)(C)C)c1OC
Reaction #598190
desired compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc([N+](=O)[O-])ccc1C(=O)OC
Reaction #601456
methyl 4-nitro-2-vinylbenzoate
Ausbeute 47.1%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1nc(C(=O)OCCCC)c(O)c2ccc(Oc3ccccc3)cc12
Reaction #611023
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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