Substructure Search

1105085

CC(C)(C)OC(=O)N1CC[C@@H]2CN(C(=O)OCc3ccccc3)C[C@@H]21
Reaction #41222
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1C[C@H]2CCN[C@H]2C1
Reaction #41223
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@]1(C)CCN(C(=O)OCc2ccccc2)C1
Reaction #45911
compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)[C@@]1(C)CCN(C(=O)OCc2ccccc2)C1
Reaction #45912
compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)[C@@]1(C)CCNC1
Reaction #45913
crude product
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
CC(C)(C)OC(=O)N(CCCF)[C@H]1CCNC1
Reaction #88587
(S)-tert-butyl 3-fluoropropyl(pyrrolidin-3-yl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC2(NC(=O)OC(C)(C)C)CNCC12
Reaction #186691
DOI: 10.1039/C8SC04228D
COC(=O)NC1CCN(C(=O)OCc2ccccc2)C1
Reaction #197817
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2C1C(C(=O)O)CN2C(=O)OCc1ccccc1
Reaction #198924
DOI: 10.1039/C8SC04228D
CN(C(=O)OC(C)(C)C)C1(C)CCN(C(=O)OCc2ccccc2)C1
Reaction #203632
DOI: 10.1039/C8SC04228D
NC1CCN(C(=O)OCc2ccccc2)C1
Reaction #223110
DOI: 10.1039/C8SC04228D
C=CC1CNCC1NC(=O)OC(C)(C)C
Reaction #225376
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC12CCCC1CNC2
Reaction #229353
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OCC1CN(C(=O)OCc2ccccc2)CC1N
Reaction #242440
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CN(C(=O)OCc2ccccc2)CC1COS(C)(=O)=O
Reaction #255525
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CN(C(=O)OCc2ccccc2)CC1COS(C)(=O)=O
Reaction #256674
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2C1C(C(=O)O)CN2C(=O)OCc1ccccc1
Reaction #266435
DOI: 10.1039/C8SC04228D
COC(=O)C1CN(C(=O)OCc2ccccc2)C2CCN(C(=O)OC(C)(C)C)C12
Reaction #267240
DOI: 10.1039/C8SC04228D
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