3-butyn-1-ol

Cc1ccn2cc(-c3ccc(C#CCCO)cc3)nc2c1
Reaction #8473
title compound
Rendement 71.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccc(NC(=O)Nc2ccc(-c3csc4c(C#CCCO)cnc(N)c34)cc2)c1
Reaction #45413
desired product
Rendement 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C#CCCOC1CCCCO1
Reaction #45465
title compound
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2ccc(N)c3c2C(=O)NC3=O)c(C#CCCO)c2ccccc21
Reaction #49385
3-amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimide
Rendement 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)c(C#CCCO)c2ccccc21
Reaction #49387
4-chloro-7-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]isoindolinone
Rendement 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2ccc(C#CCCO)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49492
4-(4-hydroxy-1-butynyl)-7-[1-(tert-butoxycarbonyl)-5-(piperidino methyl)indol-2-yl]isoindolinone
Rendement 51.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC#CCO[Si](C)(C)C(C)(C)C
Reaction #50201
title compound ( h )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
OCCC#Cc1cccnc1
Reaction #50762
4-(3-pyridyl)-1-but-3-ynol
Rendement 12.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1ccc(C#CCCO)c(OC)c1
Reaction #53385
Compound 75
Rendement 44.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
OCCC#Cc1cccc(Br)c1
Reaction #58844
4-(3-bromophenyl)but-3-yn-1-ol
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
OCCC#Cc1cnc2ccccc2c1
Reaction #81917
oil
Rendement 136.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C#CCCO[Si](C)(C)C(C)(C)C
Reaction #160489
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1ccc(C#CCCO)cc1
Reaction #187606
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(C(=O)c1ccc(F)c(C#CCCO)c1)c1ccc(OC(F)F)cc1
Reaction #196338
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1cc(C(=O)NCc2ccc(Cl)cc2)c(=O)c2cccc(C#CCCO)c21
Reaction #202612
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCCOc1ncccn1
Reaction #205667
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCCOC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #215381
4-triphenylmethyloxybut-1-yne
Rendement 53.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
OCCC#Cc1cnc2ccccc2c1
Reaction #216128
oil
Rendement 136.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
C#CCCOCC(=O)O
Reaction #216474
2-(But-3-ynyloxy)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
C#CCCOCCC(=O)OCC
Reaction #216483
Ethyl 3-(but-3-ynyloxy)propionate
Rendement 90.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
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