fluoroboric acid

Clc1ccc(C[S+](Cc2ccc(Cl)cc2)c2ccc(Cl)cc2)cc1.F[B-](F)(F)F
Reaction #6384
4-chlorophenylbis(4-chlorobenzyl)sulfonium tetrafluoroborate
Выход 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccc(C)c(F)c1
Reaction #7001
3-fluoro-4-methyl anisole
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(=Cc1ccc[nH+]c1)NC(C)=O.F[B-](F)(F)F
Reaction #7299
3-(2-Acetylamino-2-methoxycarbonylvinyl)pyridinium tetrafluoroborate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)[C@H](Cc1ccc[nH+]c1)NC(C)=O.F[B-](F)(F)F
Reaction #7300
title compound
Выход 99.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1ccc(C2COC(OC)C2)cc1
Reaction #8295
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C1CCC([PH+](C2CCCCC2)C2CCCCC2)CC1.c1ccc([B-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #42144
tricyclohexylphosphonium tetraphenylborate
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C1CSC2(S1)SCC(CSCC1CSC3(SCCS3)S1)S2
Reaction #43522
2,2′-[thiobis(methylene)]bis-1,4,6,9-tetrathiaspiro[4.4]nonane
Выход 4.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCC(C)(C)c1nc2c(C#N)c(C)c(-c3ccccc3)c(F)c2o1
Reaction #45633
compound
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCC(C)(C)c1nc2c(C#N)c(C)c(Br)c(F)c2o1
Reaction #45644
compound
Выход 106.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCC1(N2C(=O)c3ccccc3C2=O)Cc2ccccc2C1
Reaction #48005
2-(2-methoxymethylindan-2-yl)-isoindole-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCc1c(S(C)(=O)=O)c2cc(Cl)ccc2n1CC#N
Reaction #51682
[5-chloro-3-methanesulfonyl-2-(2-methoxy-ethyl)-indol-1-yl]-acetonitrile
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)c1c(Cl)cc(F)cc1Cl
Reaction #52992
2,6-dichloro-4-fluorobenzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=c1cc(-c2cccc3c2Sc2ccc(O)cc2S3)oc(N2CCOCC2)c1
Reaction #62087
title compound
Выход 100.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCCc1nc(F)c(C(=O)OCC)n1Cc1ccccc1Cl
Reaction #65265
2-n-butyl-1-{(2-chlorophenyl)methyl}-4-fluoro-5-carboethoxyimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C1C[C@@H]2CC=C[C@@H]2O1
Reaction #69435
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(C=CCC#N)cc1
Reaction #76405
4-p-tolyl-but-3-enenitrile
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=c1[nH]cnc2cc(F)ncc12
Reaction #79059
7-fluoro-4-oxo-3H-pyrido[4,3-d]pyrimidine
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1(C)CC(=O)c2cc(O)ccc21
Reaction #81557
title compound
Выход 50.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CO[C@H](C)[C@H]1COC(=O)N1c1cc(Cl)nc(Cl)n1
Reaction #85622
(R)-3-(2,6-dichloropyrimidin-4-yl)-4-((R)-1-methoxyethyl)oxazolidin-2-one
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccnc(F)c1I
Reaction #88043
2-fluoro-3-iodo-4-methoxypyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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