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11346

CCOc1ccc(C#Cc2ccc(F)c(F)c2)cc1
Reaction #4968
3,4-difluoro-4'-ethoxytolan
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1ccc(OC2CCCCO2)cc1
Reaction #10572
4-Tetrahydropyranyloxy-1-(trimethylsilylethynyl) benzene
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(OC2CCCCO2)cc1
Reaction #10573
4-Tetrahydropyranyloxyphenylacetylene
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCCCc1ccc(OCCO)cc1
Reaction #53418
114
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1
C(#Cc1ccc(OCc2ccc3ccccc3n2)cc1)c1ccncc1
Reaction #62205
2-((4-(2-(pyridin-4-yl)ethynyl)phenoxy)methyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2nc(COc3ccc(-c4nn[nH]c4-c4ccncc4)cc3)ccc2c1
Reaction #62208
solid
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc2c(c1)CCc1cc(OCCOCCOC(=O)NCCOCCOCCNC(=O)CCCCC3SCC4NC(=O)NC43)ccc1C#C2
Reaction #74292
6b
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C#Cc2ccc(CC(C)NC(=O)OC(C)(C)C)cc2)cc1
Reaction #163350
{2-[4-(4-Ethoxy-phenylethynyl)-phenyl]-1-methyl-ethyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(C#Cc2ccc(C(C)CNC(=O)OC(C)(C)C)cc2)cc1
Reaction #163351
{2-[4-(4-Propoxy-phenylethynyl)-phenyl]propyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C#Cc2ccc(C(C)NC(=O)OC(C)(C)C)cc2)cc1
Reaction #163352
{1-[4-(4-Ethoxy-phenylethynyl)-phenyl]ethyl}-carbamic acid tert-butylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C#Cc2ccc(CC(C)N)cc2)cc1.Cl
Reaction #163354
1-(4-((4-Ethoxyphenyl)ethynyl)phenyl)propan-2-amine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C#Cc2ccc(CCNC(=O)CC)cc2)cc1
Reaction #163377
N-(4-((4-Ethoxyphenyl)ethynyl)phenethyl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(C#Cc2ccc(CC(C)NC(C)=O)cc2)cc1
Reaction #163383
N-{1-Methyl-2-[4-(4-propoxy-phenylethynyl)-phenyl]-ethyl}-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C#Cc2ccc(CCNC(C)=O)nc2)cc1
Reaction #163385
N-{2-[5-(4-Ethoxy-phenylethynyl)-pyridin-2-yl]-ethyl}-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCCCc1ccc(OCCO)cc1
Reaction #168499
114
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2cc(C(C)(C)C)c(OC(C)C)c(CBr)c2C)cc1
Reaction #178153
DOI: 10.1039/C8SC04228D
Cc1c(CCCC(=O)O)c2c(F)ccc(C#Cc3ccc(OCCCCc4c(F)cc(F)c(F)c4F)cc3)c2n1CCCC(=O)O
Reaction #184719
DOI: 10.1039/C8SC04228D
CCOc1ccc(C#Cc2ccc(F)c(F)c2)cc1
Reaction #185624
DOI: 10.1039/C8SC04228D
CC(COc1ccc(C#Cc2ccc(-c3ccc(Cl)cc3)cn2)cc1)OS(C)(=O)=O
Reaction #187283
DOI: 10.1039/C8SC04228D
C[Si](C)(C)C#Cc1ccc(OCCO)c(C2NC(=O)CC(c3cccc(Cl)c3)C23C(=O)Nc2cc(Cl)ccc23)c1F
Reaction #188903
DOI: 10.1039/C8SC04228D
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