228 件の反応に参加

349571

COc1ccc(C#CCCCO)cc1
Reaction #53378
product 16
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN1C(=O)C(c2ccc(OC(F)F)cc2)(c2cccc(C#CCCCO)c2)N=C1N
Reaction #58883
title compound
収率 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)N1CCCc2cc(C#CCCCO)ccc21
Reaction #77767
6-(5-Hydroxy-pent-1-ynyl)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester
収率 93.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)OC(=O)N1CCc2cc(C#CCCCO)ccc21
Reaction #77783
5-(5-Hydroxy-pent-1-ynyl)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester
収率 105.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)OC(=O)n1ccc2cc(C#CCCCO)c(F)cc21
Reaction #77791
6-Fluoro-5-(5-hydroxy-pent-1-ynyl)-indole-1-carboxylic acid tert-butyl ester
収率 455.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)CCc1nc(C#CCCCO)ccc1O
Reaction #83591
3-[3-hydroxy-6-(5-hydroxy-1-pentynyl)-2-pyridyl]-propionic acid methyl ester
収率 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
—
Reaction #159285
60
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OCCCC#Cc1ccc(-c2ccccc2)cc1
Reaction #171527
title compound
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[Si](C)(C)C#Cc1ccc(-n2ccc3cc(C#CCCCO)ccc32)cc1
Reaction #174034
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C(=O)C(F)(F)F)c1ccc(C#CCCCO)cc1
Reaction #177726
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCc2cc(C#CCCCO)ccc21
Reaction #186659
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCCCOC(=O)NC(=O)C(c1ccccc1)c1ccccc1
Reaction #195122
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(C#CCCCO)cc1
Reaction #201390
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc[nH]c1C=C1C(=O)Nc2cccc(C#CCCCO)c21
Reaction #202273
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCCC#Cc1ccc(OC(F)(F)F)cc1
Reaction #208514
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCCCO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #215942
yellow oil
収率 1265.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
OCCCC#Cc1ccccn1
Reaction #224131
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCCCC#Cc1cccc2ccccc12
Reaction #230002
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CCCC(O)c1ccccc1
Reaction #232501
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CCCCO[Si](C)(C)C(C)(C)C
Reaction #232774
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
1 ページ次のページ