Sodium trimethylsilanolate

O=C([O-])C(F)(F)C(F)(F)C(F)(F)F.[Na+]
Reaction #4031
sodium perfluorobutyrate
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C([O-])c1ccccc1.[Na+]
Reaction #4033
sodium benzoate
Выход 322.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C([O-])c1ccc(Cl)cc1.[Na+]
Reaction #4037
Sodium 4-chlorobenzoate
Выход 94.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C([O-])C(F)(OC(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F.[Na+]
Reaction #4044
Sodium perfluoro-2-methyl-3-oxahexanoate
Выход 77.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C([O-])C(F)(OC(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F.[Na+]
Reaction #4045
Sodium perfluoro-2-methyl-3-oxahexanoate
Выход 69.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C([O-])C(F)(OC(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F.[Na+]
Reaction #4046
Sodium perfluoro-2-methyl-3-oxahexanoate
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
—
Reaction #4047
solid
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=P([O-])(c1ccccc1)c1ccccc1.[Na+]
Reaction #4056
Sodium diphenylphosphinate
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C([O-])C(F)(F)C(F)(F)F.[Na+]
Reaction #4060
Sodium perfluoropropionate
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
C[Si](C)(C)[O-].C[Si](C)(C)[O-].[Zn+2]
Reaction #362457
Zinc trimethylsilanolate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
COc1c(N)c(Cl)cc(F)c1-n1c(=O)cc(C(F)(F)F)[nH]c1=O
Reaction #362840
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CNC(=O)Cn1cc(C(=O)O)c2ccc(Cl)cc21
Reaction #592255
title compound
Выход 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=[N+]([O-])c1cc(F)c(Br)cc1O
Reaction #748258
5-bromo-4-fluoro-2-nitrophenol
Выход 205.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
C[Si](C)(C)[O-].C[Si](C)(C)[O-].[Zn+2]
Reaction #980127
Zinc trimethylsilanolate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_06
CNC(=O)Cn1cc(C(=O)O)c2ccc(Cl)cc21
Reaction #985327
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
COC(=O)c1cc(Br)cc(S(=O)(=O)Nc2ccc(C(F)(F)F)cc2)c1
Reaction #1082286
Выход 76.4%DOI: 10.26434/chemrxiv-2024-22jrqChan-Lam coupling of primary sulfonamides with boronic acids
COC(=O)c1cc(Br)cc(S(=O)(=O)Nc2ccc(OC)cc2)c1
Reaction #1082287
Выход 15.8%DOI: 10.26434/chemrxiv-2024-22jrqChan-Lam coupling of primary sulfonamides with boronic acids
COC(=O)c1oc(S(=O)(=O)Nc2ccc(C(F)(F)F)cc2)cc1C
Reaction #1082288
Выход 45.7%DOI: 10.26434/chemrxiv-2024-22jrqChan-Lam coupling of primary sulfonamides with boronic acids
COC(=O)c1oc(S(=O)(=O)Nc2ccc(OC)cc2)cc1C
Reaction #1082289
Выход 31.0%DOI: 10.26434/chemrxiv-2024-22jrqChan-Lam coupling of primary sulfonamides with boronic acids
Cc1cc(CS(=O)(=O)Nc2ccc(C(F)(F)F)cc2)no1
Reaction #1082290
Выход 70.9%DOI: 10.26434/chemrxiv-2024-22jrqChan-Lam coupling of primary sulfonamides with boronic acids
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