phosphate

NC(=O)c1ccccc1
Reaction #2781
benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
Reaction #2782
D-glucosamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O[C@@H]1C=Cc2ccccc21
Reaction #3105
(R)-inden-1-ol
Выход 46.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCOC1=C(SCCCCCC(=O)O)[C@@H](/C=C/[C@@H](O)C[C@@H](C)CCCC)[C@H](O)C1
Reaction #3122
(11R,12S,13E,15S,17S)-9-butyloxy-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoic acid
Выход 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(N)=O)[N+](C)(C)C3)[C@H](C)[C@H]12
Reaction #5154
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(=O)N(C)C)[N+](C)(C)C3)C[C@H]12
Reaction #5157
title compound
Выход 22.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=c1[nH]c(=O)c2[nH]c(=O)[nH]c2[nH]1
Reaction #5857
Uric Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(O)CCCOCc1ccccc1
Reaction #7896
title compound
Выход 102.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@H](Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8544
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H](Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8545
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@H](Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8546
title compound
Выход 47.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCO[C@@H](Cc1ccc(O)cc1)C(=O)O
Reaction #8658
(2S)-2-Ethoxy-3-(4-hydroxyphenyl)propanoic acid
Выход 40.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCO[C@@H](Cc1ccc(O)cc1)C(=O)O
Reaction #8659
(2S)-2-Ethoxy-3-(4-hydroxyphenyl)propanoic acid
Выход 40.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)C[C@H](O)C[C@H](O)COC(=O)c1ccccc1
Reaction #10226
(3R,5S)-6-benzoyloxy-3,5-dihydroxyhexanoic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)C[C@H](O)C[C@H](O)COC(=O)c1ccccc1
Reaction #10227
(3R,5S)-6-benzoyloxy-3,5-dihydroxyhexanoic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #10472
(1S,3R)-acetate
Выход 0.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ncc(Cl)cc1CCC(=O)O
Reaction #11780
title compound
Выход 25.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N[C@@H](CC1CCCCO1)C(=O)O
Reaction #47309
(S)-2-t-butoxycarbonylamino-3-(tetrahydro-pyran-2-yl)-propionic acid
Выход 71.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
Reaction #49624
D-glucosamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=C(OCc1ccccc1)N1CCC[C@H]1CO
Reaction #50038
carbobenzyloxy-L-prolinol
Выход 113.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
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