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C[C@@H]1CN(C(=O)c2ccccc2)C[C@H]1NC(=O)OC(C)(C)C
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Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(Cc2ccccc2)CC1NC(=O)OC(C)(C)C
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CN(C(=O)OC(C)(C)C)[C@H]1CCN(C(=O)c2ccccc2)C1
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Ausbeute 76.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(Cc2ccccc2)C[C@H]1NC(=O)OC(C)(C)C
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title compound
Ausbeute 35.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CNC[C@H]1NC(=O)OC(C)(C)C
Reaction #667745
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Ausbeute 87.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccccc2)C[C@H]1NC(=O)OC(C)(C)C
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title compound
Ausbeute 171.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CNC[C@H]1NC(=O)OC(C)(C)C
Reaction #667748
title compound
Ausbeute 93.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(Cc2ccccc2)CC1NC(=O)OC(C)(C)C
Reaction #903912
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CC1CN(C(=O)c2ccccc2)CC1NC(=O)OC(C)(C)C
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CC1CNCC1NC(=O)OC(C)(C)C
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C[C@H]1CNC[C@H]1NC(=O)OC(C)(C)C
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DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(C(=O)OCc2ccccc2)C[C@@H](NC(=O)OC(C)(C)C)[C@@H]1O
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sub-title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(C(=O)OCc2ccccc2)CC(NC(=O)OC(C)(C)C)C1=O
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sub-title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(Cc2ccccc2)CC1NC(=O)OC(C)(C)C
Reaction #1809472
3-(t-butoxycarbonylamino)-1-benzyl-4-methylpyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
CC1CNCC1NC(=O)OC(C)(C)C
Reaction #1809473
3-(t-butoxycarbonylamino)-4-methylpyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(C(=O)c2ccccc2)CC1
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tert-butyl N-(1-benzoylpiperidin-4-yl)carbamate
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Ausbeute 76.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)C1CCN(C(=O)c2ccccc2)C1
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