Substructure Search

CC#CCO

C#CCCC(=O)On1nnc2ccccc2c1=O
Reaction #40288
Pent-4-ynoic Acid 4-oxo-4H-benzo[d][1,2,3]triazin-3-yl Ester
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccccc1C#CC(C)(C)O
Reaction #42159
4-(N,N-dimethylaminophenyl)-2-methyl-3-butyne-2-ol
Yield 86.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccccc1C#CC(C)(C)O
Reaction #42178
4-(N,N-dimethylaminophenyl)-2-methyl-3-butyne-2-ol
Yield 86.1%DOI: 10.6084/m9.figshare.5104873.v1
OC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50176
4-hydroxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
Yield 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
Yield 96.1%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
CCOC(=O)C=C(c1cccc(OC)c1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52292
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2
Reaction #57294
11
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2)ON1C(=O)CCC1=O
Reaction #57295
12
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCC#CC(O)C1C(=O)C=CC1C=CC(O)C1CCCC1
Reaction #63768
4-(3-hydroxy-3-cyclopentyl-1-propenyl)-5-(1-hydroxy-6-methoxycarbonyl-2-hexyn-yl)-2-cyclopentenone
Yield 79.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1C#CC(=O)O)C(=O)c1c([nH]c3cc(C#N)ccc13)C2(C)C
Reaction #90067
title compound
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC=CC#CCOC1CCCCO1
Reaction #176091
DOI: 10.1039/C8SC04228D
C#CCn1c(=O)c(NC(=O)C#Cc2ccc(OC)c(OC)c2)c(N)n(CC)c1=O
Reaction #185257
DOI: 10.1039/C8SC04228D
CCCC(O)(C#Cc1cccc(CCCN)c1)CCC
Reaction #193330
DOI: 10.1039/C8SC04228D
COC(=O)C#CC(=O)c1ccc2c(c1)OCO2
Reaction #202930
DOI: 10.1039/C8SC04228D
O=C1CC2SC=CN12
Reaction #204668
DOI: 10.1039/C8SC04228D
Cc1cccc(OCC#CCC#CCC#CCC#CCCCC(=O)O)c1
Reaction #208062
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(COCC#CC(=O)O)NC(C)=C(C(=O)OC)C1c1cccc(Cl)c1Cl
Reaction #210664
DOI: 10.1039/C8SC04228D
O=C(O)CCCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2
Reaction #210788
DOI: 10.1039/C8SC04228D
CC#CCOc1cc(-c2ccc(F)cc2)ncn1
Reaction #211712
DOI: 10.1039/C8SC04228D
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