#COCCI

COCCC(CC1(C(=O)O)CCCC1)C(=O)OC(C)(C)C
Reaction #51187
crude title compound
수율 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COCCOc1ccc2[nH]ccc2c1
Reaction #69340
5-(2-methoxyethoxy)-1H-indole
수율 86.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCCC1(C(=O)OC(C)(C)C)SCCCS1
Reaction #85044
tert-Butyl 2-(2-methoxyethyl)-1,3-dithiane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COCCOc1cccc(Br)c1
Reaction #195548
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCn1ccc2ccccc21
Reaction #267664
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCC1(C(=O)OC)C=CC(NC(=O)OC(C)(C)C)C1
Reaction #296577
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCC[C@]1(C(=O)OC)C=C[C@@H](NC(=O)OC(C)(C)C)C1
Reaction #357785
desired product
수율 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COCCN1CCC(=O)CC1
Reaction #389161
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COCCC(CC1(C(=O)O)CCCC1)C(=O)OC(C)(C)C
Reaction #518949
crude title compound
수율 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
COCC[P+](CCC#N)(CCC#N)CCC#N
Reaction #755434
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COCCC(CC1(C(=O)O)CCCC1)C(=O)OC(C)(C)C
Reaction #889903
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COCCn1ccc2ccccc21
Reaction #1096191
1-(2-methoxy-ethyl)-1H-indole
수율 92.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
COCCOc1cccc2ccsc12
Reaction #1096193
7-(2-methoxy-ethoxy)-benzo[b]thiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
COCC[C@]1(C(=O)OC)C=C[C@@H](NC(=O)OC(C)(C)C)C1
Reaction #1131802
desired product
수율 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
[I-]
Reaction #1223224
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COCCOc1ccc2[nH]ccc2c1
Reaction #1307588
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COCC[C@]1(C(=O)OC)C=C[C@@H](NC(=O)OC(C)(C)C)C1
Reaction #1348873
desired product
수율 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
COCCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)[C@@H]2CCC(=O)O2)cc1
Reaction #1464380
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
COCC[P+](CCC#N)(CCC#N)CCC#N.[I-]
Reaction #1477357
Tris-(β-cyanoethyl)-2-methoxyethyl-phosphonium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_02
COCC[PH+](CCC#N)c1ccccc1.[I-]
Reaction #1477359
β-cyanoethyl-2-methoxyethyl-phenylphosphonium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_02
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