lithium tri-s-butyl borohydride

CN(C)Cc1ccc([C@H]2CC[C@@H](O)CC2)cc1
Reaction #1743
cis-4-(4-Dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC1(C(O)c2cccc([C@H]3[C@H](O)CC(=O)[C@@H]3C/C=C\CCCC(=O)NCC)c2)CCC1
Reaction #9331
alcohol
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)COCC#CC[C@@H]1[C@@H](c2ccc(C(O[Si](C)(C)C(C)(C)C)C3CCCCC3)cc2)[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1O
Reaction #9335
alcohol
Ausbeute 61.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
Reaction #44611
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1CN([C@@H](C)c2ccc(F)nc2F)C(=O)[C@@H](O)O1
Reaction #44619
title compound
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
Reaction #44639
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c3c1O[C@@H]1C[C@H](O)C=C[C@]31CCN(C)C2
Reaction #50740
(+)-galanthamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1ccc2c3c1O[C@H]1C[C@@H](O)C=C[C@@]31CCN(C)C2
Reaction #50741
(-)-galanthamine
Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(O)C(Cc1ccc(Cl)cn1)c1cccc(Br)c1
Reaction #58658
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O[C@@H]1C[C@H]2C[C@@H]1CC2(F)F
Reaction #74384
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)[Si](O[C@H]1C[C@H]2C[C@@H]1C[C@H]2O)(c1ccccc1)c1ccccc1
Reaction #74433
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)C1(C)SC(N[C@H]2C[C@H]3C[C@@H]2C[C@H]3O)=NC1=O
Reaction #74437
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(O)C(Cc1ccc(Cl)c(Cl)c1)C(=O)OC(C)(C)C
Reaction #81137
tert-butyl (2RS, 3RS)-2-(3,4-dichlorobenzyl)-3-hydroxybutanoate
Ausbeute 35.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COCc1cc(CO)no1
Reaction #82697
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCC(O)[C@@H]1CCC(=O)O1
Reaction #89017
(5S)-5-(1-hydroxypropyl)tetrahydrofuran-2-one
Ausbeute 56.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cn2ncnc(N)c2c1-c1ccc(NC(=O)Nc2cc(C(F)(F)F)ccc2F)cc1
Reaction #160882
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cn2ncnc(N)c2c1-c1ccc(NC(=O)Nc2cc(C(F)(F)F)ccn2)c(F)c1
Reaction #160894
desired compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(O)C(Cc1ccc(Cl)cn1)c1cccc(Br)c1
Reaction #220642
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C=CC[C@@H](NC(=O)OCc1ccccc1)[C@H](O)c1ccccc1
Reaction #340316
Benzyl (1R,2R)-1-hydroxy-1-phenylpent-4-en-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(O)C(C/C=C/c1ccc2ccccc2c1)c1ccc(Cl)cc1
Reaction #350859
above-identified compound
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
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