Hex-5-enoic acid

C=CCCCCCCCCCNC(=O)CCCC=C
Reaction #90837
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=CCCCC(=O)OC(C)(C)C
Reaction #173954
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCC=CCCCC(=O)O
Reaction #411096
5-decenoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
C=CCCCC(=O)OC(C)(C)C
Reaction #510077
t-butyl ester
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C=CCCCC(=O)N[C@@H](Cc1cc(Cl)cc(Cl)c1)[C@H](O)CN[C@H]1C[C@@H](OCC=C)c2ccc(OC)cc21
Reaction #588943
N-((2S,3R)-4-((1S,3R)-3-(allyloxy)-6-methoxy-2,3-dihydro-1H-inden-1-ylamino)-1-(3,5-dichlorophenyl)-3-hydroxy-butan-2-yl)hex-5-enamide
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
C=CCCCC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)CN[C@@H]1C[C@@H](OCC=C)c2ccc(Br)cc21
Reaction #588944
N-((2S,3R)-4-((1R,3R)-3-(allyloxy)-6-bromo-2,3-dihydro-1H-inden-1-ylamino)-1-(3,5-difluorophenyl)-3-hydroxybutan-2-yl)hex-5-enamide
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
C=CCCCC(=O)N[C@@H](CC(C)C)[C@@H](CN[C@H]1C[C@@H](OCC=C)c2ccc(OC(C)C)cc21)O[Si](C)(C)C(C)(C)C
Reaction #588945
N-((2R,3S)-1-((1S,3R)-3-(allyloxy)-6-isopropoxy-2,3-dihydro-1H-inden-1-ylamino)-2-(tert-butyldimethylsilyloxy)-5-methylhexan-3-yl)hex-5-enamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
C=CCCCC(=O)O[C@H]1C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](/C=C/[C@H](COc2cccc(C(F)(F)F)c2)O[Si](CC)(CC)CC)[C@H]1CC=C
Reaction #604563
title compound
Ausbeute 90.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
C=CCCCC(=O)OC
Reaction #742292
Hex-5-enoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
C=CCCCC(=O)NC(Cc1cc(Cl)cc(Cl)c1)C(O)CNC1CC(OCC=C)c2ccc(OC)cc21
Reaction #781512
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
C=CCCCC(=O)NC(Cc1cc(F)cc(F)c1)C(O)CNC1CC(OCC=C)c2ccc(Br)cc21
Reaction #894512
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCC=CC(=O)[C@]1(O)CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #947885
3-hexenoyl cholesterol
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_12
C=CCCCC(=O)OC
Reaction #990733
Methyl 5-hexenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_10
C=CCCCC(=O)OC
Reaction #1118770
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_09
C=CCCCC(=O)NC(CC(C)C)C(CNC1CC(OCC=C)c2ccc(OC(C)C)cc21)O[Si](C)(C)C(C)(C)C
Reaction #1238431
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
C=CCCCC(=O)CP(=O)(OC)OC
Reaction #1476229
dimethyl 2-oxo-6-heptenylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_01
C=CCCCCCCCCCNC(=O)CCCC=C
Reaction #1606097
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
C=CCCCC(=O)OC(C)(C)C
Reaction #1730586
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
C=CCCCC(=O)O[C@@H]1CO[C@H]2[C@@H]1OC[C@H]2O
Reaction #1763177
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
C=CCCCC(=O)OC(C)(C)C
Reaction #1763178
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
Seite 1Weiter