borane tetrahydrofuran

COC(=O)c1cccc(N2CCCCC2)c1
Reaction #2432
oil
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(O)C1CCCCC1
Reaction #4601
1-methyl-1-cyclohexylmethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
OCc1ccc(CBr)cc1
Reaction #6022
title compound
Yield 94.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
OCc1cc2ccccc2cn1
Reaction #7243
3-(hydroxymethyl)isoquinoline
Yield 12.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1cccnc1CO
Reaction #7247
alcohol
Yield 124.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CSc1ncccc1CO
Reaction #7258
title compound
Yield 30.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OCc1cccnc1O
Reaction #7263
alcohol
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ncccc1CO
Reaction #7264
alcohol
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1ccc(CN2CCCCC2)cc1
Reaction #11619
1-(4-nitro-benzyl)-piperidine
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(C)c([N+]2=CN(c3ccccc3O)CC2)c(C)c1.[Cl-]
Reaction #11833
desired product
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NCC1(CN)CCOCC1
Reaction #40785
yellow oil
Yield 62.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)OCc2cc([C@@H](O)CBr)ccc2O1
Reaction #42733
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1cc(CO)cc(C(F)(F)F)c1
Reaction #45332
[3-nitro-5-(trifluoromethyl)phenyl]methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](c1ccccc1)N1CC[C@](C)(NC(=O)OC(C)(C)C)C1
Reaction #45909
compound
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)Cc1nc(-c2ccc(OCCN3CCN(c4ccncc4)CC3)cc2)cn1-c1ccc(Oc2ccc(Cl)cc2)cc1
Reaction #46023
1-[2-(4-{1-[4-(4-Chloro-phenoxy)-phenyl]-2-isobutyl-1H-imidazol-4-yl}-phenoxy)-ethyl]-4-pyridin-4-yl-piperazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NCc1ccc(N)c2ccccc12
Reaction #47196
4-(aminomethyl)naphthalen-1-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(NCCCCCCN1CC(O)CC1CO)OCc1ccccc1
Reaction #49179
compound 29
Yield 92.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc([C@@H]2CCCN2C)on1
Reaction #50037
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(C)(C)OC(=O)N1CCC(CO)CC1
Reaction #52236
l-Boc-piperidine-4-methanol
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=[N+]([O-])c1ccc(O)c(CO)c1
Reaction #52566
2-hydroxymethyl-4-nitrophenol
Yield 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
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