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C#CCCCO

C#CCC1C(=O)N(C)OC1c1ccccc1
Reaction #907
2-methyl-5-phenyl-4-propargylisoxazolin-3-one
Ausbeute 34.5%DOI: 10.6084/m9.figshare.5104873.v1
C#CCCCOC1CCCCO1
Reaction #2031
1-(Tetrahydopyran-2-yloxy)-4-pentyne
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC#CCCCOC1CCCCO1
Reaction #2037
title compound ( 15 )
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[O-].CC(=O)[O-].[Ni+2]
Reaction #2038
nickel acetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC#Cc1ccccc1
Reaction #6818
5-phenylpent-4-ynoic acid
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCC#Cc1ccccc1
Reaction #6819
(4-phenyl-but-3-ynyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C#CCCCN=[N+]=[N-])cc1
Reaction #49890
product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50176
4-hydroxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
Ausbeute 88.3%DOI: 10.6084/m9.figshare.5104873.v1
COC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50177
4-methoxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
Ausbeute 96.1%DOI: 10.6084/m9.figshare.5104873.v1
COC1(C#CCO)CCOCC1
Reaction #50178
4-methoxy-4-(3-hydroxyprop-1-ynyl)tetrahydropyran
Ausbeute 47.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOCO[C@H]1CC[C@@]2(C)[C@H](CC[C@@H]3[C@@H]2CC[C@]2(C)C(O)(CCC(=O)O)CC[C@]32O)C1
Reaction #50277
17-hydroxy-17-(2-carboxyethyl)-3beta-ethoxymethoxy-14-hydroxy-5beta,14beta-androstane
DOI: 10.6084/m9.figshare.5104873.v1
OCCCC#Cc1cc2cc[nH]c2cc1F
Reaction #77792
5-(6-Fluoro-1H-indol-5-yl)-pent-4-yn-1-ol
Ausbeute 843.9%DOI: 10.6084/m9.figshare.5104873.v1
OCCCC#Cc1cc2c(cc1F)NCC2
Reaction #77793
5-(6-Fluoro-2,3-dihydro-1H-indol-5-yl)-pent-4-yn-1-ol
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(O)CCC#CC
Reaction #94185
2-methyloct-1-en-6-yn-3-ol
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #162528
( 4.66 )
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C#CCCC(=O)O)cc1
Reaction #188675
DOI: 10.1039/C8SC04228D
CCC(CC)(c1ccc(O)c(C)c1)c1ccc(C=CC2(O)CCOCC2)c(C)c1
Reaction #191434
DOI: 10.1039/C8SC04228D
CC#CC(CC(=O)O)c1ccc(OCC2=CC3(CCCC3)CCC2)cc1
Reaction #204010
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C1C(C#CC(=O)OCC(Cl)(Cl)Cl)C1(C)C
Reaction #208497
DOI: 10.1039/C8SC04228D
C(#Cc1ccccc1)C1=NOC2(CCC3(CC2)OCCO3)C1
Reaction #208820
DOI: 10.1039/C8SC04228D
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