Recherche de Sous-structure

16760063

CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1603
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #1605
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #1607
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1670
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #1673
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #1675
product
DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cc2ccccc2cc1C(=O)OC
Reaction #1714
title compound
Rendement 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2175
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #2178
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #2180
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2216
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #2219
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #2221
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2274
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #2277
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #2279
product
DOI: 10.6084/m9.figshare.5104873.v1
C#CCN(OC)C(=O)OC
Reaction #3498
methyl N-methoxy-N-propargylcarbamate
Rendement 58.7%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN(OC)C(=O)c1ccc(Cl)cc1
Reaction #3500
N-methoxy-N-propargyl-p-chlorobenzamide
Rendement 36.5%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOC(=NOC)c1ccc(Cl)cc1Cl
Reaction #3501
propargyl N-methoxy-2,4-dichlorobenzimidate
Rendement 29.8%DOI: 10.6084/m9.figshare.5104873.v1
C#CCn1c(-c2cc(Cl)nc(Cl)c2)nn(C(C)(C)C)c1=O
Reaction #3716
2-(t-butyl)-5-(2,6-dichloro-4-pyridyl)-4-propargyl-1,2,4-triazolin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
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