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C#Cc1ccc(N)cc1

CC1(C)CCNc2ccc(C#C[Si](C)(C)C)cc21
Reaction #6652
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc2c(c1)C(C)(C)CCN2
Reaction #6653
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52407
oil
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52408
oil
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Nc1cc([N+](=O)[O-])ccc1C#CC(C)C
Reaction #68396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc2ccc([N+](=O)[O-])cc2[nH]1
Reaction #68397
title compound
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
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccc(Cl)cc1)N1CCc2cc(C#CCCCO)c(F)cc21
Reaction #77794
6-Fluoro-5-(5-hydroxy-pent-1-ynyl)-2,3-dihydro-indole-1-carboxylic acid 4-chloro-phenyl ester
Выход 74.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)N2CCc3cc(C#CCCCOS(C)(=O)=O)c(F)cc32)cc1
Reaction #77798
Methanesulfonic acid 5-[6-fluoro-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-indol-5-yl]-pent-4-ynyl ester
Выход 94.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCO)CCCC#Cc1cc2c(cc1F)N(S(=O)(=O)c1ccc(C)cc1)CC2
Reaction #77799
2-(Ethyl-{5-[6-fluoro-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-indol-5-yl]-pent-4-ynyl}-amino)-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79976
oil
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79977
oil
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc2c(c1)C(C)(C)CC(=O)N2
Reaction #80716
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)Nc2cc(C#C[Si](C)(C)C)ccc21
Reaction #80724
title compound
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc2c(c1)NC(=O)CC2(C)C
Reaction #80725
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CC(=O)N3Cc2ccccc2)cc1
Reaction #80732
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCN1C(=O)CC(C)(C)c2cc(C#Cc3ccc(C(=O)OCC)cc3)ccc21
Reaction #80733
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(N)c(C#N)c1C
Reaction #80917
2-amino-5-ethynyl-6-methylbenzonitrile
Выход 106.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC#Cc1ccc(N)c([N+](=O)[O-])c1
Reaction #86436
title compound
Выход 100.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2c(F)cccc2Cl)nn1-c1ccc(C#Cc2ccc(F)nc2)cc1
Reaction #87700
desired product
Выход 23.0%DOI: 10.6084/m9.figshare.5104873.v1
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