Substructure Search

1409088

C=Cc1ccc(C(O)(C(=O)OC2CCN(C(=O)OC(C)(C)C)CC2)C2CCC(F)(F)C2)cc1
Reaction #185476
DOI: 10.1039/C8SC04228D
CCN1CCC(OC(=O)C(O)(c2ccc(Cl)cc2)C2CCC(F)(F)C2)CC1
Reaction #197690
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(O)C1CCCC1)C(=O)C1(N)C(=O)N(CC2CC2)c2ccccc2N(CC2CC2)C1=O
Reaction #205956
DOI: 10.1039/C8SC04228D
CN(C)C1CCN(C(=O)C(O)(c2ccccc2)C2CCCC2)CC1
Reaction #211189
DOI: 10.1039/C8SC04228D
C[C@H](NC(=O)C(O)C1CCCC1)C(=O)C1(N)C(=O)N(CC2CC2)c2ccccc2N(CC2CC2)C1=O
Reaction #220474
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C(O)C1CCCC1)C(=O)NC1C(=O)N(CC(C)(C)C)c2ccccc2N(CC(C)(C)C)C1=O
Reaction #220477
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1OC(=O)C(C2=CCCC2)(c2ccccc2)O1
Reaction #229304
DOI: 10.1039/C8SC04228D
[Cl-]
Reaction #234765
DOI: 10.1039/C8SC04228D
O=C(O)C(O)(c1ccccc1)C1CCC(F)(F)C1
Reaction #235018
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #248148
DOI: 10.1039/C8SC04228D
N=CN1CCC(CCOC(=O)C(O)(c2ccccc2)C2CCC(F)(F)C2)CC1
Reaction #258545
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(OC(=O)C(O)(c2ccccc2)C2CCCC2)C1
Reaction #263772
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #278051
DOI: 10.1039/C8SC04228D
O=C(OC1CN2CCC1CC2)C(O)(c1cccs1)C1CCCC1
Reaction #298523
DOI: 10.1039/C8SC04228D
CCOC(=O)C(O)(c1ccccc1)C1CCCC1
Reaction #300041
DOI: 10.1039/C8SC04228D
CCOC(=O)C(O)(CC(C)(C)c1ccccc1)C1CCCC1
Reaction #301252
DOI: 10.1039/C8SC04228D
CC(C)(C)[C@H]1OC(=O)[C@](c2ccccc2)(C2(O)CCCC2)O1
Reaction #305219
intermediate ( 1b )
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1OC(=O)[C@](C2=CCCC2)(c2ccccc2)O1
Reaction #305220
intermediate ( 1c )
Yield 89.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCNCC1)[C@](O)(c1ccccc1)C1CCCC1
Reaction #305222
title compound
Yield 68.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@@H](OC(=O)[C@](O)(c2ccccc2)C2CCCC2)C1
Reaction #305223
(R)-3-((R)-2-Cyclopentyl-2-hydroxy-2-phenylacetoxy)pyrrolidine-1-carboxylic acid t-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
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