allyl alcohol

C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2009
N-(t-Butoxycarbonyl)-D-homophenylalanine allyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@@H](COCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2018
N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOCC1=C(C(=O)O)N2C(=O)C(N)[C@H]2SC1
Reaction #5254
3-allyloxymethyl-7-amino-ceph-3-eme-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCOc1nc(-c2ccncc2)nc(NS(=O)(=O)Nc2ccc(C(C)C)cc2)c1Oc1ccccc1OC
Reaction #10345
4-i-propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CS(=O)(=O)Nc1cccc(CCC=O)c1
Reaction #44177
title compound
Yield 60.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=C(CO)c1c(-c2ccccc2)c(C)c(C#N)c2nc(C3CC3)oc12
Reaction #45895
compound
Yield 32.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CCOC(=O)[C@H](C)Nc1ccc(Cl)c(Cl)c1
Reaction #51311
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCOC(=O)COc1ccc(Cl)c(Cl)c1
Reaction #51866
title compound
Yield 96.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCOCc1csc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51916
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccccc1-c1ccc2c(c1)C(CNc1ccccc1)=CC(C)(C)N2
Reaction #54034
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCOC(=O)CC1(CN)CCCCC1.Cl
Reaction #58793
product ( 13 )
Yield 88.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CCC(C)(C=O)c1cc([N+](=O)[O-])ccc1F
Reaction #59103
2-(2-fluoro-5-nitrophenyl)-2-methylpent-4-enal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CCOC(=O)CCCOc1cc([N+](=O)[O-])c(CO)cc1OC
Reaction #62268
product
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CCOC(C)OCC
Reaction #63005
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
C=CCOC(=N)N1Cc2ccccc2-c2ccccc2C1
Reaction #63441
allyl 5,7-dihydro-6H-dibenz[c,e]azepine-6-carboximidate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
C=CCO.C=CCOC(C)=O
Reaction #65607
Allyl Alcohol Allyl Acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C=CCOC(=N)C(Cl)(Cl)Cl
Reaction #81082
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=CCOC(=O)CP(=O)(OCC)OCC
Reaction #81150
allyl diethylphosphonoacetate
Yield 82.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=CCOC[C@H](NC(=O)OC(C)(C)C)C(=O)OC
Reaction #86651
(S)-3-Allyloxy-2-tert-butoxycarbonylamino-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=CCOC1O[C@H](CO)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #87464
((2R,3R,4S,5R)-6-allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yl)-methanol
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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