isopropylmagnesium chloride lithium chloride

Cn1cc(B2OC(C)(C)C(C)(C)O2)c(-c2ccc(F)cc2)n1
Reaction #70155
3-(4-fluorophenyl)-1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCc1ccc(B(O)O)cc1C1C(=O)C2CCC(C2)C1=O
Reaction #159448
3-(2,4-dioxo-bicyclo[3.2.1]oct-3-yl)-4-ethylphenylboronic acid
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(Cl)c(C(C)C(O)c2ccnc(Cl)c2)c1
Reaction #420989
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C(c1nccs1)C(F)F
Reaction #497564
2,2-difluoro-1-(1,3-thiazol-2-yl)ethanone
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(C)(C)OC(=O)C1CCC(O)(c2nccs2)CC1
Reaction #497622
tert-butyl 4-hydroxy-4-(1,3-thiazol-2-yl)cyclohexanecarboxylate
Ausbeute 80.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
O=C(c1cc(Cl)cc(Cl)c1O)C(F)(F)F
Reaction #531873
ketone
Ausbeute 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Cn1cncc1C(=O)c1ccc(C(F)(F)F)nc1
Reaction #608020
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cn1cncc1C(O)c1ccccn1
Reaction #608023
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCCC(O)c1ccc(C(=O)OCC)cc1
Reaction #624606
ethyl 4-(1-hydroxybutyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
COC(=O)c1ccc(C(O)CC2CC2)cc1
Reaction #624614
(+/−)-methyl 4-(2-cyclopropyl-1-hydroxyethyl)benzoate
Ausbeute 45.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCOC(=O)c1ccc(C(=O)C2CCCC2)cc1
Reaction #624620
ethyl 4-(cyclopentanecarbonyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CC(C)CC(O)c1ccc(Br)cc1
Reaction #624621
(+/−)-1-(4-bromophenyl)-3-methylbutan-1-ol
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
COC(=O)c1ccc(C(O)CC(C)(C)C)cc1
Reaction #624625
(+/−)-methyl 4-(1-hydroxy-3,3-dimethylbutyl)benzoate
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCOC(=O)c1ccc(C(O)CC(C)C)cc1
Reaction #624629
ethyl 4-(1-hydroxy-3-methylbutyl)benzoate
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCOC(=O)c1ccc(C(=O)C2CC(C)(C)C2)cc1
Reaction #624643
ethyl 4-(3,3-dimethylcyclobutanecarbonyl)benzoate
Ausbeute 83.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCOC(=O)c1ccc(C(O)CCC(F)(F)F)cc1
Reaction #624754
(+/−)-ethyl 4-(4,4,4-trifluoro-1-hydroxybutyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
O=C1c2cc(Br)ccc2CC12CCC(C(F)(F)F)CC2
Reaction #626490
title compound
Ausbeute 52.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
O=C1c2cc(Br)ccc2CC12CCC(C(F)F)CC2
Reaction #626498
title compound
Ausbeute 36.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CC(C)c1nc2c(c(I)c1[C@@H](O)c1cc(F)c([Si](C)(C)C)c(F)c1)[C@@H](O[Si](C)(C)C(C)(C)C)CC(C)(C)C2
Reaction #660893
(S)—((S)-5-(tert-butyldimethylsilyloxy)-4-iodo-2-isopropyl-7,7-dimethyl-5,6,7,8-tetrahydroquinolin-3-yl)(3,5-difluoro-4-(trimethylsilyl)phenyl)methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(C)Oc1ccc([C@H](O)c2c(C(C)C)nc3c(c2I)[C@@H](O[Si](C)(C)C(C)(C)C)CC(C)(C)C3)cc1
Reaction #660895
(S)—((S)-5-(tert-butyldimethylsilyloxy)-4-iodo-2-isopropyl-7,7-dimethyl-5,6,7,8-tetrahydroquinolin-3-yl)(4-isopropoxyphenyl)methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
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