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CC#C

CCCCC#CC#CCOc1ccc(C(=O)OCC)cc1
Reaction #2735
ethyl 4-(2,4-nonadiynyloxy)-benzoate
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC#CC1(O)C(=O)Nc2ccc(Br)cc21
Reaction #7087
5-bromo-3-hydroxy-3-prop-1-ynyl-1,3-dihydroindol-2-one
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(C#Cc3ccccc3)c2c1
Reaction #7340
2-(3-Fluoro-4-hydroxyphenyl)-4-(phenylethynyl)quinolin-6-ol
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccccc1C1(OCCCOC2(c3ccccc3C#C)C=CN3C(=O)c4cc(OC)ccc4N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]32)C=CN2C(=O)c3cc(OC)ccc3N(C(=O)OCC(Cl)(Cl)Cl)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]21
Reaction #47142
17
Выход 92.7%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(COC2(C)CC2)c(C(C)C)c1
Reaction #52543
4-Ethynyl-2-isopropyl-1-(1-methyl-cyclopropoxymethyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc(COC3(C)CC3)c(C(C)C)c2)cc1
Reaction #52544
title compound
Выход 60.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CCC#CC(O)CC2=C(C)CCC2=O)c1
Reaction #55935
3-methyl-2-[6-(m-methoxyphenyl)-2-hydroxy-3-hexynyl]-2-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCCc2cn(C#Cc3ccccc3)c3cccc1c23
Reaction #61564
17
Выход 55.2%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1cccc2[nH]ncc12
Reaction #66501
4-(trimethylsilyl)ethynyl-1H-indazole
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN(Cc1cc2c(=O)n(C)c(CN(CC)CC)nc2cc1Cl)c1ccc(C(=O)OC(C)(C)C)cc1
Reaction #76131
tert-Butyl 4-[N-[2-Diethylaminomethyl-7-chloro-3-methyl-4-oxo-3,4-dihydroquinazolin-6-ylmethyl]-N-(prop-2-ynyl)amino]benzoate
DOI: 10.6084/m9.figshare.5104873.v1
C#CCN(Cc1cc2c(=O)n(C)c(CN(CC)CC)nc2cc1Cl)c1ccc(C(=O)NCc2cccnc2)cc1
Reaction #76141
4-[N-[2-Diethylaminomethyl-7-chloro-3-methyl-4-oxo-3,4-dihydroquinazolin-6-ylmethyl]-N-(prop-2-ynyl)amino]-N-(3-pyridylmethyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nc(C#Cc2cccc(C)c2)n1C
Reaction #77221
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nc(C#Cc2ccc(Cl)cc2)n1C
Reaction #77227
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nc(C#Cc2ccc(F)cc2)n1C
Reaction #77228
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(COC2(C)CC2)c(C(C)C)c1
Reaction #80109
4-Ethynyl-2-isopropyl-1-(1-methyl-cyclopropoxymethyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1nc(C#Cc2cccc(NS(=O)(=O)C(F)(F)F)c2)ccc1OCCCC/C=C/c1ccc(OC)cc1
Reaction #83587
3-{3-[6-(4-methoxyphenyl)-(5E)-5-hexenyloxy]-6-[2-(3-trifluoromethanesulfonamidophenyl)-ethinyl]-2-pyridyl}-propionic acid methyl ester
Выход 32.7%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2c(F)cccc2Cl)nn1-c1ccc(C#Cc2ccccc2C(F)(F)F)cc1
Reaction #87698
desired product
Выход 27.4%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
O=c1[nH]c(-c2c(F)cccc2Cl)nn1-c1ccc(C#Cc2ccc(Cl)cc2F)cc1
Reaction #87701
desired product
Выход 31.9%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2c(F)cccc2Cl)nn1-c1ccc(C#Cc2ccc(C(F)(F)F)cc2Cl)cc1
Reaction #87702
desired product
Выход 25.5%DOI: 10.6084/m9.figshare.5104873.v1
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