methyl 3(R)-hydroxybutyrate

COC(=O)C[C@H](C)SC(C)=O
Reaction #50704
title compound
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COC(=O)[C@H](Cc1ccc(Cl)c(Cl)c1)[C@@H](C)O
Reaction #81140
methyl (2R, 3R)-2-(3,4-dichlorobenzyl)-3-hydroxybutyrate
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)C1=C(O)C(=O)O[C@@H]1C
Reaction #83731
(R)-2-hydroxy-3-methoxycarbonyl-2-penten-4-olide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)C[C@H](C)SC(C)=O
Reaction #414104
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
COC(=O)[C@@H](C)[C@@H](C)O
Reaction #414105
methyl 3-(R)-hydroxy-2-(S)methylbutanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
COC(=O)C[C@H](C)SC(C)=O
Reaction #429184
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COC(=O)[C@@H](C)[C@@H](C)O
Reaction #429185
methyl 3-(R)-hydroxy-2-(S)-methylbutanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COC(=O)[C@H](Cc1ccc(Cl)c(Cl)c1)[C@@H](C)O
Reaction #463374
methyl (2R, 3R)-2-(3,4-dichlorobenzyl)-3-hydroxybutyrate
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
COC(=O)[C@H](C/C=C/c1ccccc1)[C@@H](C)O
Reaction #652411
methyl (2R,3R)-2-[(2E)-3-phenyl-2-propen-1-yl]-3-hydroxybutanoate
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
COC(=O)C[C@H](C)SC(C)=O
Reaction #952651
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_10
COC(=O)[C@@H](C)[C@@H](C)O
Reaction #952652
methyl 3-(R)-hydroxy-2-(S)-methylbutanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_10
COC(=O)[C@H](C/C=C/c1ccccc1)[C@@H](C)O
Reaction #975121
methyl (2R,3R)-2-[(2E)-3-phenyl-2-propen-1-yl]-3-hydroxybutanoate
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
COC(=O)C1=C(O)C(=O)O[C@@H]1C
Reaction #1121016
(R)-2-hydroxy-3-methoxycarbonyl-2-penten-4-olide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_05
COC(=O)C[C@@H](C)OS(=O)(=O)c1ccc(C)cc1
Reaction #1160516
Methyl (R)-3-(p-Toluenesulfonyloxy)butyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_11
COC(=O)C[C@@H](C)O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #1330387
(R)-3-(tert-butyl-diphenyl-silanyloxy)-butyric acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
COC(=O)[C@H](Cc1ccc(Cl)c(Cl)c1)[C@@H](C)O
Reaction #1539604
methyl (2R, 3R)-2-(3,4-dichlorobenzyl)-3-hydroxybutyrate
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
COC(=O)C[C@@H](C)O.OCCCCO
Reaction #1794503
titled oligomer
Выход 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_10
COC(=O)C[C@@H](C)O[Si](C)(C)C(C)(C)C
Reaction #1973179
methyl (R)-β-t-butyldimethylsilyloxybutyrate
Выход 84.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_09
COC(=O)[C@H](Cc1ccc(Cl)c(Cl)c1)[C@@H](C)O
Reaction #2043252
methyl (2R,3R)-2-(3,4-dichlorobenzyl)-3-hydroxybutyrate
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07
COC(=O)[C@H](C/C=C/c1ccccc1)[C@@H](C)O
Reaction #2356521
methyl (2R,3R)-2-[(2E)-3-phenyl-2-propen-1-yl]-3-hydroxybutanoate
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_12
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