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CC1(C)CC(O)CC(C)(C)N1

CC1(C)CC(OC(=O)CS(=O)(=O)C(C)(C)C)CC(C)(C)N1
Reaction #54461
2,2,6,6-tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C(C)(C)CC(OC(=O)C(Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)(Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C(C)=O)CC1(C)C
Reaction #54462
1-acetyl-2,2,6,6-tetramethyl-4-piperidinyl 2,2-bis-(3,5-di-tert-butyl-4-hydroxybenzyl)-acetoacetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCCCCC1NCC2(CC(C)(C)NC(C)(C)C2)O1
Reaction #55499
2-iso-Octyl-7,7,9,9-tetramethyl-1-oxa-3,8-diaza-spiro-[4,5]-decane
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(OC(=O)C(Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C(=O)OC2CC(C)(C)NC(C)(C)C2)CC(C)(C)N1
Reaction #55627
3,5-di-tert.butyl-4-hydroxybenzyl-malonic acid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester
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
—
Reaction #95322
exo-2,3-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1
Reaction #174031
DOI: 10.1039/C8SC04228D
CN1C(C)(C)CC(OCCC#N)CC1(C)C
Reaction #174257
DOI: 10.1039/C8SC04228D
CC(C)(C)NC(=O)C1(O)CC(C)(C)NC(C)(C)C1
Reaction #185182
DOI: 10.1039/C8SC04228D
CC1(C)CC(OCCOc2ccc(-c3nc4ccccc4o3)cc2)CC(C)(C)N1
Reaction #185370
DOI: 10.1039/C8SC04228D
CN1C(C)(C)CC(N=O)(OC(=O)C(C)(C)C)CC1(C)C
Reaction #187800
DOI: 10.1039/C8SC04228D
CC1(C)CC(O)CC(C)(C)N1c1nc(N2CCOCC2)nc(N2CCOCC2)n1
Reaction #192622
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(C)CC(OC(=O)Nc2ccccc2)CC(C)(C)N1CC(O)c1ccccc1
Reaction #203484
DOI: 10.1039/C8SC04228D
CC1(C)CC(OC(=O)c2ccccc2)CC(C)(C)N1OC1CCCCC1O
Reaction #212183
DOI: 10.1039/C8SC04228D
CC(C)N(c1nc(Cl)nc(N2C(C)(C)CC3(CC2(C)C)OCCO3)n1)C(C)C
Reaction #213690
DOI: 10.1039/C8SC04228D
CN1C(C)(C)CC(OC(=O)N=NC(=O)OC2CC(C)(C)N(C)C(C)(C)C2)CC1(C)C
Reaction #217144
title compound
Ausbeute 23.4%DOI: 10.6084/m9.figshare.5104873.v1
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