ethenoxyethane

O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1033
4-bromo-3-chloro-3,4,4-trifiuorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC1CCC(C(C)=O)=NO1
Reaction #4372
title compound
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
C=COC1CCC=C1Br
Reaction #9365
1-bromo-5-vinyloxy-cyclopentene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(OCCI)[C@@H](CO[Si](C)(C)C(C)(C)C)NC(=O)OC(C)(C)C
Reaction #48617
desired compound
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(C)OC[C@H]1CCC(=O)N1
Reaction #51243
(5R)-5-(1-ethoxyethoxymethyl)pyrrolidin-2-one
収率 102.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(C)OC(/C=C/I)C1CC(CC)C1
Reaction #55573
title compound
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOC(C)OC(CC=C(C)C)C(C)CCOC(C)=O
Reaction #55929
8-acetoxy-2,6-dimethyl-5-[(1-ethoxyethoxy)]-2-octene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
C=COC1CCC=C1Br
Reaction #57006
1-bromo-5-vinyloxy-cyclopentene
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
CC1=C2OC(C)OC2CC(C)(C)C1=O
Reaction #83997
2,4,6,6-tetramethyl-7,7a-dihydro-6H-benzo[1,3]dioxol-5-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(C)OC(C#N)C(OC)c1ccc(N2CCOCC2)cc1
Reaction #84859
2-(1-ethoxyethoxy)-3-methoxy-3-(4-morpholinophenyl)propanenitrile
収率 35.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(C)O[C@H](COS(=O)(=O)c1ccc(C)cc1)CN(Cc1ccccc1)[C@@H](CC(=O)OC)C(=O)OCc1ccccc1
Reaction #89716
1-benzyl 4-methyl(2S)-2-[benzyl((2S)-2-(1-ethoxyethoxy)-3-[(4-methylphenyl)sulfony]oxypropyl)amino]succinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(C)O[C@@H](COS(=O)(=O)c1ccc(C)cc1)CN(Cc1ccccc1)[C@@H](CC(=O)OC)C(=O)OCc1ccccc1
Reaction #89729
1-benzyl 4-methyl(2S)-2-[benzyl((2R)-2-(1-ethoxyethoxy)-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=CCCC(OC=C)C(c1ccccc1)c1ccccc1
Reaction #166076
1,1-diphenyl-2-(1-ethenoxy)-hex-5-ene
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC1CC(=O)N1C
Reaction #179383
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(C)OCc1cc(F)ccc1Br
Reaction #182293
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(C)OC(CBr)COc1ccc2cnn(CC(C)O[Si](C)(C)C(C)(C)C)c2c1Br
Reaction #184300
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(C)Oc1ccc(C#N)cc1OC
Reaction #190518
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(C)OCc1cc(OC)ccc1Br
Reaction #193588
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCCC=P(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #197603
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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