Substructure Search

CC(C)NCCO

C[C@H]1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)C(=O)O1
Reaction #44610
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
Reaction #44611
title compound
Yield 97.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)C(=O)O1
Reaction #44638
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
Reaction #44639
title compound
Yield 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)N(CCC)CCC)c2)C1
Reaction #49234
title compound
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #49235
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2CC(O)(c3ccccc3)CN2)c1
Reaction #49236
title compound
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cc(C)cc(C(=O)N3CCC[C@@H]3COC)c2)C1
Reaction #49239
title compound
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCO)C(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #51996
product
Yield 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC=O)C(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #51997
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(C)(C)C)C(O)c1ccc(OC(=O)c2ccc3c(c2)OCO3)c2[nH]c(=O)ccc12
Reaction #56066
8-(3,4-methylenedioxyphenylcarbonyloxy)-5-(1-hydroxy-2-tert-butylaminopropyl)carbostyril
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2c(C(O)CNC3(Cc4ccc(C(F)(F)F)cc4)CC3)ccc(OCc3ccccc3)c2[nH]1
Reaction #58131
8-benzyloxy-5-{1-hydroxy-2-[1-(4-trifluoromethyl-benzyl)-cyclopropylamino]-ethyl}-1H-quinolin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2c(C(O)CNC3(Cc4ccc(C(F)(F)F)cc4)CC3)ccc(O)c2[nH]1
Reaction #58132
8-hydroxy-5-{1-hydroxy-2-[1-(4-trifluoromethyl-benzyl)-cyclopropylamino]-ethyl}-1H-quinolin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(NC(=O)C1CC2CCCCC2N1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(O)C(=O)OCC
Reaction #70196
32
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1C[C@@H](O)C[C@@]1(C[C@@H](O)[C@@H](N)Cc1ccccc1)C(N)=O.N#N
Reaction #82386
N2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-4(S)-hydroxy-L-prolinamide
Yield 98.6%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CO)NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #168605
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C=O)NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #168607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](NC(c1ccccc1)(c1ccccc1)c1ccccc1)[C@@H](C)O
Reaction #168609
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](NC(c1ccccc1)(c1ccccc1)c1ccccc1)C(C)=O
Reaction #168617
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(N)C(O)C(=O)NC1CC1
Reaction #176047
DOI: 10.1039/C8SC04228D
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