3-iodoprop-1-ene

C=CCn1nc(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)c(Cc2ccc(CC)cc2)c1C
Reaction #7487
1-allyl-4-[(4-ethylphenyl)methyl]-3-(β-D-glucopyranosyloxy)-5-methyl-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCC1(C(=O)OC(C)(C)C)CCc2ncc(NC(=O)OCc3ccccc3)c(=O)n21
Reaction #11070
intermediate 20a
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCOC[C@H](NC(=O)OC(C)(C)C)[C@H]1CO1
Reaction #48320
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CCN(C(=O)c1ccccc1)N(C(=O)c1ccccc1)C(C)(C)C
Reaction #49907
N-allyl-N'-t-butyl-N,N'-dibenzoylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
C=CCOC1CN(C(=O)OC(C)(C)C)CCC1(OC)OC
Reaction #71934
title compound
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CCN1C(C)(c2cccc(Br)c2)COS1(=O)=O
Reaction #160456
3-allyl-4-(3-bromophenyl)-4-methyl-[1,2,3]-oxathiazolidine-2,2-dioxide
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCC1(S(=O)(=O)OCCCC)CC1
Reaction #160575
titled product
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCOc1ccc(O)cc1
Reaction #173074
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCn1c(=O)ccc2c1cc(F)c[n+]2[O-]
Reaction #174079
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOc1cccc(C(=O)OC)c1
Reaction #176475
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCN1CCN(C(=O)OCc2ccccc2)CC1=O
Reaction #180150
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOc1ccc2cn[nH]c2c1
Reaction #196088
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCC(C(=O)N1C(=O)OCC1Cc1ccccc1)c1ccccc1
Reaction #209728
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCc1cc(C(=O)OCC)ccc1NC(C)=O
Reaction #213820
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCC(C(=O)O)C(C)(C)c1ccccc1
Reaction #221027
oil
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C=CCn1nc(-c2ccc3ccccc3c2)c2c(N)ncnc21
Reaction #233704
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCC1CC(c2cccc(C(F)(F)F)c2)N(c2ccc(Oc3ccc(Cl)cc3)cc2)C1=O
Reaction #238601
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
[I-]
Reaction #239839
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCON=C(C(=O)OCC)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #243364
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCSC(=N)c1nn(-c2c(Cl)cc(C(F)(F)F)cc2Br)c(N)c1S(C)=O
Reaction #245633
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Seite 1Weiter