(−)cinchonidine

COCCOCN1C(C)=C(C(=O)O)[C@@H](c2cccc([N+](=O)[O-])c2)C(C(=O)OC)=C1C
Reaction #62680
(R)-1-(2-methoxyethoxy)methyl-2,6-dimethyl-3-carbomethoxy-4-(3-nitrophenyl)-5-carboxy-1,4-dihydropyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
C=C[C@H]1CN2CC[C@H]1C[C@H]2[C@H](O)c1ccnc2ccccc12.O=C(O)C[C@H](C(=O)O)c1c[nH]c2ccccc12
Reaction #440598
(S)-indole-3-succinic acid cinchonidine
المردود 13.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
C=C[C@H]1CN2CC[C@H]1C[C@H]2[C@H](O)c1ccnc2ccccc12.C[C@H](C(=O)O)c1cccc(C(=O)c2ccccc2)c1
Reaction #460538
salt
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
CCCCCC[C@H](C(=O)O)n1cnc([N+](=O)[O-])c1
Reaction #462304
(R)-2-(4-nitro-1H-imidazol-1-yl)-octanoic acid
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
C=C[C@H]1CN2CC[C@H]1C[C@@H]2[C@@H](O)c1ccnc2ccccc12
Reaction #538018
(+)-Cinchonine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
C=C[C@H]1CN2CC[C@H]1C[C@H]2[C@H](O)c1ccnc2ccccc12
Reaction #747262
L-cinchonidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Cc1sc2c(c1C)C(c1ccc(Cl)cc1)=N[C@@H](CC(=O)O)c1nnc(C)n1-2
Reaction #814441
(S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
CC(=O)C(NC(=O)N(C)C)(C(C)=O)[C@@H](/C=C/c1ccccc1)NC(=O)OCc1ccccc1
Reaction #1144040
diketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
O=C1OC(c2ccc(-c3ccccc3)cc2)C(O)=C1O
Reaction #1253772
5-[(1,1′-biphenyl)-4-yl]-3,4-dihydroxy-2(5H)-furanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_09
COc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #1501856
6-methoxy-2-naphthyl-α-methylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_01
c1ccc2[nH]ccc2c1
Reaction #1680814
indole
المردود 157.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_11
CCCCCC[C@H](C(=O)O)n1cnc([N+](=O)[O-])c1
Reaction #1696950
(R)-2-(4-nitro-1H-imidazol-1-yl)-octanoic acid
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_03
COC(=O)[C@H](O)c1ccccc1
Reaction #1726671
(R)-methyl mandelate
المردود 88.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
COC(=O)[C@H](O)c1ccccc1
Reaction #1726672
(R)-methyl mandelate
المردود 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
COC(=O)[C@H](O)c1ccccc1
Reaction #1726673
(R)-methyl mandelate
المردود 96.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
COC(=O)[C@H](O)c1ccccc1
Reaction #1726674
(R)-methyl mandelate
المردود 99.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
COC(=O)[C@H](O)c1ccccc1
Reaction #1726675
(R)-methyl mandelate
المردود 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
—
Reaction #1768408
peptide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_12
CCCCCC[C@H](C(=O)O)n1cnc([N+](=O)[O-])c1
Reaction #1856460
(R)-2-(4-nitro-1H-imidazol-1-yl)-octanoic acid
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_01
C=C[C@H]1CN2CC[C@H]1C[C@H]2[C@H](OC(=O)c1ccc(OCCCCCC)cc1)c1ccnc2ccccc12
Reaction #1880942
(R)-1-(4-quinolyl)-1-[(2S,4S,5R)-5-vinyl-1-azabicyclo[2.2.2]oct-2-yl]methyl 4-(hexyloxy)benzoate
المردود 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
الصفحة 1التالي