β-NAD

O=P([O-])([O-])[O-]
Reaction #7441
Phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NC(=O)c1ccc[n+]([C@@H]2O[C@H](COP(=O)([O-])OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)c1.O=C1CCC(=O)N1O
Reaction #463664
N-hydroxysuccinimide nicotinamide adenine dinucleotide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCCOC(=O)Cc1c2n(c3ccccc13)C[C@H](N)CC2
Reaction #562670
crude title compound
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(C)(C)OC(=O)N1CCC2(CC2)[C@H](O)C1
Reaction #646514
title compound
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O[C@@H]1CN(Cc2ccccc2)CCC12CC2
Reaction #646521
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CC(C)(C)OC(=O)N1CCC2(CC2)[C@H](O)C1
Reaction #742672
title compound
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CCOC(=O)C[C@H](O)CCl
Reaction #806255
ethyl (S) 4-chloro-3-hydroxybutyrate
Rendement 85.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
O[C@@H]1CN(Cc2ccccc2)CCC12CC2
Reaction #1183361
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CCOC(=O)C[C@H](O)CCl
Reaction #1244290
ethyl (S) 4-chloro-3-hydroxybutyrate
Rendement 85.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
CCOC(=O)C[C@H](O)CCl
Reaction #1332459
ethyl (S) 4-chloro-3-hydroxybutyrate
Rendement 85.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
O=C1OC[C@@H]2CCCC[C@H]12
Reaction #1504041
(1R,6S)-(+)-8-oxabicyclo[4.3.0]nonan-7-one
Rendement 87.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
O=C1OC[C@@H]2CCC[C@H]12
Reaction #1504042
(1R,5S)-(+)-7-oxabicyclo[3.3.0]octan-6-one
Rendement 92.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
O=C1OCC[C@@H]1c1ccccc1
Reaction #1504043
(R)-2-phenylbutyrolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
O=C1OCC[C@H]1Cc1ccccc1
Reaction #1504044
(R)-2-benzylbutyrolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
O=C1OCC[C@H]1CCCF
Reaction #1504045
(2R)-2-(3-fluoropropyl)butyrolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
O=C1OCC[C@@H]1C(=O)c1ncc[nH]1
Reaction #1504046
(2R)-2-imidazoylbutyrolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
O=C1OCC[C@@H]1c1ccc(F)cc1
Reaction #1504047
(2R)-2-(4-fluorophenyl)butyrolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
O=C1OCC[C@@H]1C1CCCCC1
Reaction #1504048
(2R)-2-cydohexylbutyrolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
COc1ccc([C@H]2CCOC2=O)cc1
Reaction #1504049
(2R)-2-(4-methoxyphenyl)butyrolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
COc1ccc([C@H]2CCOC2=O)cc1OC
Reaction #1504050
(2R)-2-(3,4-dimethoxyphenyl)butyrolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
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