5-hexynoic acid

C#CCCCC(=O)N1NCCCC1C(=O)C(=O)C(C)(C)CC
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DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)CCCC#CCc1ccccc1
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DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)CCCC#Cc1cccc(OC)c1
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oil
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C#CCCCC(=O)N1C(=O)OC[C@@H]1c1ccccc1
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title compound
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O=C1CCC/C(=C\Br)O1
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product
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Cc1noc(-c2ccc(C#CCCCC(=O)O)cc2)c1NC(=O)OC(C)c1ccccc1Cl
Reaction #383691
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C#CCCCC(=O)OC
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methyl 5-hexynoate
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C#CCCCC(=O)OC
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methyl 5-hexynoate
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C#CCCCC(=O)N1CCOCC1
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title compound ( 11 )
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C#CCCCC(=O)N1C(=O)OC[C@@H]1c1ccccc1
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title compound
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C#CCCCC(=O)N1C(=O)OC[C@@H]1Cc1ccccc1
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title compound
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
C#CCCCC(=O)OCC1(C)COC1
Reaction #520065
title compound
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—
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Intermediate B
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C#CCCCC(=O)N1CCOCC1
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title compound ( 11 )
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CC(CO)NC(=O)c1cccc(C#CCCCC(=O)O)c1
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CC(CO)NC(=O)c1cccc(C#CCCCC(=O)O)c1
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( 4 )
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C#CCCCC(=O)N1C(=O)OC[C@@H]1c1ccccc1
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title compound
Rendimiento 85.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
O=C(O)CCCC#CCc1ccccc1
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C#CCCCC(=O)OC
Reaction #897675
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C#CCCCC(=O)N1C(=O)OCC1c1ccccc1
Reaction #913179
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