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9175

CC12CCC(C(=O)N(CCCCN3CCN(c4ncccn4)CC3)C1=O)C2(C)C
Reaction #5013
title compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCC(C2)C(=O)N1CCCCN1CCN(c2ncccn2)CC1
Reaction #5014
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2CCC1C(=O)N(CCCCN1CCN(c3ncccn3)CC1)C2=O
Reaction #5016
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC(C)(C1)C(=O)N(CCCCN1CCN(c3ncccn3)CC1)C2=O
Reaction #5017
title compound
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2CCC1C2
Reaction #5020
anhydride
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CC(C(=O)N1CCCCN1CCN(c3cncc(Cl)n3)CC1)C1CC=CC21
Reaction #224359
DOI: 10.1039/C8SC04228D
CC12CCC(C(=O)N(CCc3ccccn3)C1=O)C2(C)C
Reaction #235939
DOI: 10.1039/C8SC04228D
O=C(O)C1CCC(C(=O)N(Cc2ccccc2)OCc2ccccc2)C1
Reaction #384282
DOI: 10.1039/C8SC04228D
CC1(C)C2CCC1C(=O)N(CCCCN1CCN(c3ncccn3)CC1)C2=O
Reaction #402306
DOI: 10.1039/C8SC04228D
O=C(O)[C@H]1CC[C@@H](C(=O)N(Cc2ccccc2)OCc2ccccc2)C1
Reaction #442519
product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #708962
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #708964
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2CCC1C2
Reaction #898645
DOI: 10.1039/C8SC04228D
CC12CCC(C(=O)OC1=O)C2(C)C
Reaction #909698
DOI: 10.1039/C8SC04228D
CC12CCC(C(=O)N(CCc3ccccn3)C1=O)C2(C)C
Reaction #955126
1,8,8-Trimethyl-3-[2-(2-pyridinyl)ethyl]-3-azabicyclo[3.2.1]octane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC(C)(C1)C(=O)N(CCCCN1CCN(c3ncccn3)CC1)C2=O
Reaction #1046076
DOI: 10.1039/C8SC04228D
CC1(C)C2CC[C@@]1(C)C(=O)OC2=O
Reaction #1105878
(1R)-camphoric anhydride
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2CC[C@@]1(C)C(=O)OC2=O
Reaction #1105879
(1R)-camphoric anhydride
Ausbeute 90.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCC(C2)C(=O)N1CCCCN1CCN(c2cccc(Cl)c2)CC1
Reaction #1221202
DOI: 10.1039/C8SC04228D
CC12CCC(C(=O)OC1=O)C2(C)C
Reaction #1221436
DOI: 10.1039/C8SC04228D
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