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1313903

NC(=O)C1CCOCC1
Reaction #9565
tetrahydropyran-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCOCC1
Reaction #9628
methyl tetrahydro-2H-pyran-4-carboxylate
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CC(=O)OC(C)(C)C)CCOCC1
Reaction #9629
methyl 4-(2-tert-butoxy-2-oxoethyl)tetrahydro-2H-pyran-4-carboxylate
Ausbeute 56.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CC(=O)c2ccc(Br)cc2)CCOCC1
Reaction #9631
methyl 4-[2-(4-bromo-phenyl)-2-oxoethyl]tetrahydro-2H-pyran-4-carboxylate
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CC(=O)c2ccc(-c3ccc([N+](=O)[O-])cc3)cc2)CCOCC1
Reaction #9632
methyl 4-[2-(4′-nitro-1,1′-biphenyl-4-yl)-2-oxoethyl]tetrahydro-2H-pyran-4-carboxylate
Ausbeute 79.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCOCC1
Reaction #41216
solid
Ausbeute 94.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(C#N)CCOCC1
Reaction #44853
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(CN)CCOCC1
Reaction #44854
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(CN2CCC(=O)CC2)CCOCC1
Reaction #44855
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(CN2CCC(C#N)CC2)CCOCC1
Reaction #44856
title compound
Ausbeute 63.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(CN2CCC(CN)CC2)CCOCC1
Reaction #44857
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)OC(C)(C)C)CCOCC3)CC2)c2ccccc21
Reaction #44858
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCOCC3)CC2)c2ccccc21
Reaction #44859
title compound
Ausbeute 92.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(O[Si](C)(C)C)=C1CCOCC1
Reaction #44861
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1CCN(CC2(C(=O)O)CCOCC2)CC1
Reaction #44862
titled compound
Ausbeute 65.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.NCC1CCN(CC2(C(=O)O)CCOCC2)CC1
Reaction #44863
titled compound
Ausbeute 87.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCOCC3)CC2)c2ccccc21
Reaction #44864
titled compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCOCC3)CC2)c2ccccc21.O=S(=O)(O)c1ccccc1
Reaction #44865
titled compound
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)C1CCOCC1
Reaction #44886
title compound
Ausbeute 70.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C(C)=O)CCOCC1
Reaction #46978
4-acetyl-4-methoxycarbonyltetrahydropyran
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
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