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222950

OC1(C#Cc2ccc(-c3ccccn3)cc2)CN2CCC1CC2
Reaction #398678
DOI: 10.1039/C8SC04228D
C#Cc1ccc(-c2nc(C(=O)OC)c(OC)c(N)c2F)cc1
Reaction #494418
title compound
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(-c2ccc(C#C[Si](C)(C)C)cc2)c(C)c(N)c1Cl
Reaction #603761
title compound
Ausbeute 21.1%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(-c2nc(C(=O)OC)c(Cl)c(N)c2C)cc1
Reaction #603762
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(-c2ccc(C#C[Si](C)(C)C)cc2)c(F)c(N)c1Cl
Reaction #603763
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(-c2nc(C(=O)OC)c(Cl)c(N)c2F)cc1
Reaction #603764
title compound
Ausbeute 97.6%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(-c2nc(C(=O)OC)c(Cl)c(N)c2F)cc1F
Reaction #603765
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(-c2nc(C(=O)OC)c(Cl)c(N)c2C)cc1F
Reaction #603766
title compound
Ausbeute 69.9%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(-c2nc(C(=O)OC)c(C=C)c(N)c2F)cc1
Reaction #603767
title compound
Ausbeute 61.8%DOI: 10.6084/m9.figshare.5104873.v1
OC1(C#Cc2ccc(-c3ccccn3)cc2)CN2CCC1CC2
Reaction #948587
3-[2-(4-[2-pyridyl]phenyl)ethynyl]-3-hydroxyquinuclidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C#Cc2ccc(-c3nc4nc(O[C@@H]5CO[C@H]6[C@@H]5OC[C@H]6O[Si](C)(C)C(C)(C)C)n(COCC[Si](C)(C)C)c4cc3Cl)cc2)CC1
Reaction #1016348
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@@H]1CO[C@H]2[C@@H]1OC[C@H]2Oc1nc2nc(-c3ccc(C#CC4CCNCC4)cc3)c(Cl)cc2n1COCC[Si](C)(C)C
Reaction #1016349
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(C1CC1)N1CCC(C#Cc2ccc(-c3nc4nc(O[C@@H]5CO[C@H]6[C@@H]5OC[C@H]6O)[nH]c4cc3Cl)cc2)CC1
Reaction #1016419
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2cc3cnc(-c4ccc(C(C)=O)cc4)cc3s2)CC1
Reaction #1094123
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2nc(-c3ccc(C#CCO)cc3)cc3sccc23)CC1.c1ccncc1
Reaction #1094230
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(-c2nc3nc(O[C@H]4CO[C@H](CO)[C@@H](O)C4)[nH]c3cc2Cl)cc1
Reaction #1137440
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nnc(C#Cc2ccc(-c3nc4nc(O[C@H]5CO[C@H](CO)[C@@H](O)C5)[nH]c4cc3Cl)cc2)n1
Reaction #1137456
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(-c2cc3sc(N4CCN(CC)CC4)cc3cn2)cc1
Reaction #1338356
title compound
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2cc3cnc(-c4ccc(C(C)=O)cc4)cc3s2)CC1
Reaction #1338357
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1ccc(-c2ccccn2)cc1
Reaction #1609892
2-(4-trimethylsilylethynylphenyl)pyridine
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
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