Substructure Search

[Pd]

Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #111
Yield 81.0%
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #112
Yield 88.0%
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #113
Yield 73.0%
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #114
Yield 79.0%
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #115
Yield 85.0%
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #116
Yield 85.0%
c1cc2cn[nH]c2cc1N1CCCC1
Reaction #648
Yield 93.7%
Cc1cc(N2CCN(C)[C@@H](C)C2)ncc1-c1ccc(-c2nc3c(CO)cccc3c(=O)[nH]2)cc1
Reaction #752
Yield 26.5%
Cc1cc(N2CCN(C)[C@@H](C)C2)ncc1-c1ccc(-c2nc3c(CO)cccc3c(=O)[nH]2)cc1
Reaction #753
Yield 34.7%
CC[C@H](NC(=O)[C@H](NC(=O)[C@@H](N)CC(=O)O)[C@H](C)O)c1ccccc1
Reaction #864
α-L-aspartyl-D-threonine (S)-α-ethylbenzylamide
Yield 57.5%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](NC(=O)[C@H](NC(=O)[C@@H](N)CC(=O)O)[C@H](C)CC)c1ccccc1
Reaction #866
α-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide
Yield 72.3%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](NC(=O)[C@H](NC(=O)[C@@H](N)CC(=O)O)C(C)C)c1ccccc1
Reaction #870
α-L-aspartyl-D-valine (R)-α-methoxymethylbenzylamide
Yield 70.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H](NC(=O)[C@H](NC(=O)[C@@H](N)CC(=O)O)C(C)C)c1ccccc1
Reaction #872
α-L-aspartyl-D-valine (R)-α-ethoxymethylbenzylamide
Yield 50.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N)ccc2c1C(=O)NS2(=O)=O
Reaction #905
4-Methyl-5-aminosaccharin
DOI: 10.6084/m9.figshare.5104873.v1
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)CC1
Reaction #957
4-Aminoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCC1CCNC1
Reaction #964
(3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1CNC1
Reaction #966
title compound
Yield 67.1%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CCCC2OCCCO2)nc1
Reaction #982
acetal
Yield 92.5%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(Oc2ccc(C3CCNCC3)cc2)cc1
Reaction #1047
compound ( 4 )
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC#Cc1cncc(C2CCCN2C)c1
Reaction #1137
5-propynyl-3-(1-methyl-2-pyrrolidinyl)pyridine
Yield 312.1%DOI: 10.6084/m9.figshare.5104873.v1
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