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417469

O=C(OCc1ccccc1)N1CCC(NCCO)CC1
Reaction #48494
title compound
Yield 107.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC(N2CCOCC2=O)CC1
Reaction #48495
title compound
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OCCC)C2)oc1CC
Reaction #71938
title compound
Yield 86.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OCCC)C2)oc1C
Reaction #71942
title compound
Yield 86.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(NC(=O)OCc2ccccc2)CC1
Reaction #72100
title compound
Yield 74.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCNCC1)OCc1ccccc1
Reaction #72101
title compound
Yield 86.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(C(=O)OCc2ccccc2)C1
Reaction #88585
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(CCCF)[C@H]1CCN(C(=O)OCc2ccccc2)C1
Reaction #88586
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC1CCN(C(=O)OCc2ccccc2)C1
Reaction #197817
DOI: 10.1039/C8SC04228D
NC1CCN(C(=O)OCc2ccccc2)C1
Reaction #223110
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC(N)C1
Reaction #251044
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCN(C(=O)OCc2ccccc2)C1
Reaction #278519
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCN(C(=O)C2CCN(C(=O)OCc3ccccc3)CC2)C1
Reaction #282934
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N[C@H]1CCNC1
Reaction #319227
title compound
Yield 98.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(NC(=O)OCc2ccccc2)CC1
Reaction #371427
DOI: 10.1039/C8SC04228D
CCCCOC(=O)N1CCN(C(=O)C(N)CCCCOCc2ccccc2)CC1
Reaction #386922
DOI: 10.1039/C8SC04228D
CCCCOC(=O)N1CCC(CCCc2ccccc2)C(O)C1
Reaction #387233
DOI: 10.1039/C8SC04228D
CCN(C(=O)NC)C1CCN(C(=O)OCc2ccccc2)CC1
Reaction #404021
DOI: 10.1039/C8SC04228D
O=C(OCc1ccccc1)N1CCC(NC2CCCCC2)C1
Reaction #407793
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N[C@H]1CCN(C(=O)OCc2ccccc2)C1
Reaction #426035
(S)-benzyl 3-(tert-butoxycarbonylamino)pyrrolidine-1-carboxylate
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
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