#1109071

C=CC(=O)Oc1ccccc1
Reaction #3163
reddish brown liquid
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CC(=O)OCCOCCN1C(=O)C2CCCCC2C1=O
Reaction #3165
orange-red liquid
Ausbeute 59.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CC(=O)OCC1CNC(=O)O1
Reaction #3168
5-Acryloyloxymethyl-oxazolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CC(=O)N(C1CCCCC1)C1CCCCC1
Reaction #5588
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)NC12CC3CC(CC(C3)C1)C2
Reaction #5590
N-tricyclo[3.3.1.13,7 ]dec-1-yl-2-propenamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)NC1CCC2CC1C2(C)C
Reaction #5592
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)NC1C2CC3CC(C2)CC1C3
Reaction #5593
N-tricyclo [3.3.1.13,7 ]dec-2-yl-2-propenamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)N1CC2CCC(CC2)C1
Reaction #5595
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)Nc1ccc2oc(C)nc2c1
Reaction #5602
5-acrylamido-2-methyl benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccccc21
Reaction #5920
2-(4-chlorophenyl)-4-acryloyl-3,4-dihyro-2H-1,4-benzothiazine
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccc3ccccc3c21
Reaction #5928
3-(4-chlorophenyl)-1-propenoyl-2,3-dihydro-1H-naphtho[2,1-b][1,4]thiazine
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)OCC1COC(OC)(c2ccccc2)O1
Reaction #6287
4-acryloyloxymethyl-2-methoxy-2-phenyl-1,3-dioxolane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)OC12CC3CC(CC(C3)C1C)C2
Reaction #7289
2-methyladamantyl acrylate
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(=O)Nc1c(C)cccc1C(=O)NC(C)C
Reaction #7499
product
Ausbeute 52.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(=O)N(C)Cc1c[nH]c2ccccc12
Reaction #46523
title compound
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CC(=O)N(C)Cc1cc2cccnc2n1C
Reaction #46537
title compound
Ausbeute 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CC(=O)N(C)Cc1c(C)[nH]c2ccccc12
Reaction #46587
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CC(=O)N(C)Cc1cn(C)c2ccccc12
Reaction #46600
N-(1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(O)cc1
Reaction #46941
MEHQ
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(O)cc1
Reaction #46942
MEHQ
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Seite 1Weiter