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122562

CON1C(C)(C)CC(OC(=O)CCc2cc(-n3nc4ccc(Cl)cc4n3)c(O)c(C(C)(C)C)c2)CC1(C)C
Reaction #56602
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)CON1C(C)(C)CC(OC(=O)c2ccc3nn(-c4cc(C(C)(C)C)cc(C(C)(C)c5ccc(Cl)cc5)c4O)nc3c2)CC1(C)C
Reaction #56604
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(CCC(=O)OC2CC(C)(C)N(Oc3ccc(Br)cc3Br)C(C)(C)C2)cc(-n2nc3ccc(Cl)cc3n2)c1O
Reaction #56607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(CCC(=O)OC2CC(C)(C)N(Oc3ccc(Cl)cc3[N+](=O)[O-])C(C)(C)C2)cc(-n2nc3ccc(Cl)cc3n2)c1O
Reaction #56608
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CC(C)(C)N(OC2CCCCC2)C(C)(C)C1
Reaction #80666
1-Cyclohexyloxy-2,2,6,6-tetramethyl-4-acetoxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #80667
1-Cyclohexyloxy-2,2,6,6-tetramethyl-4-hydroxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCON1C(C)(C)CC(OCC2CO2)CC1(C)C
Reaction #80668
1-Octyloxy-2,2,6,6-tetramethyl-4-(2,3-epoxypropoxy)piperidine
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1
Reaction #174031
DOI: 10.1039/C8SC04228D
CC(C)(CON1C(C)(C)CC(OC(=O)c2ccccc2)CC1(C)C)c1ccccc1
Reaction #181384
DOI: 10.1039/C8SC04228D
CC1(C)CC(OC(=O)c2ccccc2)CC(C)(C)N1OC(N)=O
Reaction #198035
DOI: 10.1039/C8SC04228D
CC(=O)N1C(C)(C)CC(Oc2nc(OC3CC(C)(C)N(O)C(C)(C)C3)nc(N3C(C)(C)CCCC3(C)C)n2)CC1(C)C
Reaction #199608
DOI: 10.1039/C8SC04228D
CC1(ON2C(C)(C)CC(OC(=O)c3ccccc3)CC2(C)C)CCCCC1
Reaction #207784
DOI: 10.1039/C8SC04228D
CC1(C)CC(OC(=O)c2ccccc2)CC(C)(C)N1OC1CCCCC1O
Reaction #212183
DOI: 10.1039/C8SC04228D
CON1C(C)(C)CC(OC(=O)NNC(=O)OC2CC(C)(C)N(OC)C(C)(C)C2)CC1(C)C
Reaction #217139
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(OC(=O)NNC(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1
Reaction #217140
title compound
Ausbeute 54.5%DOI: 10.6084/m9.figshare.5104873.v1
CON1C(C)(C)CC(OC(=O)N=NC(=O)OC2CC(C)(C)N(OC)C(C)(C)C2)CC1(C)C
Reaction #217142
desired product
Ausbeute 113.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCON1C(C)(C)CC(OC(=O)NNC(=O)OC2CC(C)(C)N(OCCCCCCCC)C(C)(C)C2)CC1(C)C
Reaction #217143
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCON1C(C)(C)CC(OC(=O)N=NC(=O)OC2CC(C)(C)N(OCCCCCCCC)C(C)(C)C2)CC1(C)C
Reaction #217145
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(OC(=O)N=NC(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1
Reaction #217146
title compound
Ausbeute 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CON1C(C)(C)CC(OC(=O)Cl)CC1(C)C
Reaction #217147
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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