1-heptyne

CCCC#Cc1ccc2c(Cl)c(O)ccc2c1
Reaction #40268
1-chloro-6-(1-pentynyl)-2-naphthol
수율 88.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCC#Cc1cc(OC)ccc1C(=O)OC
Reaction #231012
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCC#CCC(OC)OC
Reaction #372844
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCC#CC(O)(Cn1cncn1)C(C)(C)C
Reaction #446110
title compound
수율 26.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
CCCCCC#Cc1sccc1Br
Reaction #508016
2-heptynyl 3-bromothiophene
수율 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CCCCCC#Cc1ccccc1NC(C)=O
Reaction #538434
N-(2-Hept-1ynyl-phenyl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCCCCC#Cc1ccc(C(=O)OC)cc1NC(C)=O
Reaction #538440
3-Acetylamino-4-hept-1-ynyl-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCCCCC#Cc1ccc(C(C)=O)cc1OC
Reaction #538441
1-(4-Hept-1-ynyl-3-methoxy-phenyl)ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCCCCC#Cc1ccc(C=O)cc1
Reaction #538448
4-Hept-1-ynyl-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCCCCC#Cc1ccc(OC(F)(F)F)cc1
Reaction #538453
1-Hept-1-ynyl-4-trifluoromethoxy-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCCCCC#Cc1cc(F)cc(Cl)c1
Reaction #538458
1-Chloro-3-fluoro-5-hept-1-ynyl-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCCCCC#Cc1sccc1Br
Reaction #580626
2-heptynyl 3-bromothiophene
수율 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
C=CCC#CCCCCC
Reaction #606427
desired compound
수율 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
C=CCC#CCCCCC
Reaction #682809
desired compound
수율 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCCCCC#Cc1cn(S(=O)(=O)c2ccccc2)nc1-c1cccnc1
Reaction #747339
3-(1-phenylsulfonyl-4-hept-1-ynyl-1H-pyrazol-3-yl)-pyridine
수율 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CCCCCC#Cc1sccc1Br
Reaction #774406
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCCCC#Cc1cc(-c2ccccc2)nn1C
Reaction #896166
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCCCC#Cc1ccc(C(C)=O)cc1OC
Reaction #911773
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCCCC#C[Si]1(C)CCC1
Reaction #913542
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCCCC#Cc1ccc(C=O)cc1
Reaction #914645
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
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