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235943

CCC[CH2][Sn]([C]#CC1CCN(C(=O)OC(C)(C)C)CC1)([CH2]CCC)[CH2]CCC
Reaction #198421
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(CCCO)CC1
Reaction #225091
DOI: 10.1039/C8SC04228D
COC(=O)C#CC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #227609
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OCC#CC1CCNCC1
Reaction #232254
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(C#Cc2ccc3ncnc(Cl)c3c2)CC1
Reaction #236480
DOI: 10.1039/C8SC04228D
COC(=O)C#CC1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #238840
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(C#Cc2ccccc2)CC1
Reaction #244704
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(O)(C#CCO)CC1
Reaction #246195
DOI: 10.1039/C8SC04228D
Cl
Reaction #293571
DOI: 10.1039/C8SC04228D
CCC[CH2][Sn]([C]#CC1CCN(C(=O)OC(C)(C)C)CC1)([CH2]CCC)[CH2]CCC
Reaction #365382
title compound
Ausbeute 86.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C#Cc2ncccn2)CC1
Reaction #382104
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(C#Cc2ccccc2)CC1
Reaction #387249
DOI: 10.1039/C8SC04228D
C(#CC1CCNCC1)c1ccccc1
Reaction #388607
DOI: 10.1039/C8SC04228D
C#CC1(O)CCN(C(=O)OC(C)(C)C)CC1
Reaction #453915
N-Boc-4-hydroxy-4-ethynyl-piperidine
DOI: 10.6084/m9.figshare.5104873.v1
C#CC1(O)CCN(C(=O)OC(C)(C)C)CC1
Reaction #468077
N-Boc-4-hydroxy-4-ethynyl-piperidine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C#CC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #546684
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C#CC1(O)CCN(C(=O)OC(C)(C)C)CC1
Reaction #546685
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C#CC1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #546686
title compound
Ausbeute 54.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(C#CCO[Si](C)(C)C(C)(C)C)CC1
Reaction #602029
title compound
Ausbeute 121.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)OC1(C#CCO[Si](C)(C)C(C)(C)C)CCN(C(=O)OC(C)(C)C)CC1
Reaction #602030
title compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
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