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1069648

COC(=O)CC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #60658
title compound
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)COC(=O)C2
Reaction #75620
tert-butyl 3-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CC2(CCNCC2)CO1
Reaction #75621
3-oxo-2-oxa-8-azaspiro[4.5]decane hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCC1(Sc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)CCN(C(=O)OC(C)(C)C)CC1
Reaction #178234
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(C(CCCCl)C(=O)O)CC1
Reaction #191698
DOI: 10.1039/C8SC04228D
CCOC(=O)CC1(Sc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)CCN(C(=O)OC(C)(C)C)CC1
Reaction #206750
DOI: 10.1039/C8SC04228D
COC(=O)CC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #219382
Title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccccc1[N+](=O)[O-])C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #219383
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C2Cc3ccccc3NC2=O)CC1
Reaction #219384
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccccc1[N+](=O)[O-])N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #219387
Title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C1CCN(C(=O)OC(C)(C)C)CC1)C(O)c1cccnc1NC(=O)C(C)(C)C
Reaction #219400
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C1CCN(C(=O)OC(C)(C)C)CC1)C(O)c1cnccc1NC(=O)C(C)(C)C
Reaction #219401
Title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2ccncc2cc1C1CCNCC1
Reaction #219402
Title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c2nc(F)ccc2cc1C1CCNCC1
Reaction #219418
expected product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #219515
Title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccccc1[N+](=O)[O-])C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #219516
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C2Cc3ccccc3NC2=O)CC1
Reaction #219517
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccccc1[N+](=O)[O-])N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #219520
Title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C1CCN(C(=O)OC(C)(C)C)CC1)C(O)c1cccnc1NC(=O)C(C)(C)C
Reaction #219535
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=c1[nH]c2ncccc2cc1C1CCNCC1
Reaction #219536
Title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
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