borane

CC1=C2CC(CC1)C2(C)C
Reaction #4793
pinene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
OCc1ncccc1CCNCc1ccccc1
Reaction #7284
benzyl-2-[2-(hydroxymethyl)-pyridin-3-yl]-ethylamine
收率 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OCc1cc(-c2ccc(Cl)cc2)oc1C(F)(F)F
Reaction #9732
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1ccc(CN2CCCCC2)cc1
Reaction #11619
1-(4-nitro-benzyl)-piperidine
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(N[C@H]1Cc2ccccc2N(CCO)C1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11678
title compound
收率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)CC1CCCC2CC(CC)OC12O
Reaction #40887
desired title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1ccc2c([C@@H](O)CBr)ccc(OCc3ccccc3)c2[nH]1
Reaction #42725
title compound
收率 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
OCCc1cccc(I)c1
Reaction #44170
title compound
收率 92.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)Cc1ccccc1Sc1c[nH]c2ccccc12
Reaction #44892
[2-(1H-Indol-3-ylsulfanyl)benzyl]dimethyl amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)Cc1ccccc1Sc1c[nH]c2ccccc12
Reaction #44916
[2-(1H-Indol-3-ylsulfanyl)benzyl]dimethyl amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)[C@H](CCO)NC(=O)OCc1ccccc1
Reaction #47606
(S)-2-benzyloxycarbonylamino-4-hydroxy-butyric acid methyl ester
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C12CCC(CCCO)(CC1)CC2
Reaction #51134
methyl 4-(3-hydroxypropyl)bicyclo[2.2.2]octane-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cc2ccc(C3CCCC(N)C3)nc2cc1OC
Reaction #51617
light-yellow solid
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCCCCCCO
Reaction #55586
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
C[C@]12CCC[C@H](O)[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](OC3CCCCO3)CC[C@@H]12
Reaction #55610
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Cl.c1ccc(CN2CC[C@@H]3[C@@H](C2)c2ccccc2N3c2ccccc2)cc1
Reaction #56188
trans-2-benzyl-2,3,4,4a,5,9b-hexahydro-5-phenyl-1H-pyrido[4,3-b]indole Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC(C)(C)OC(=O)NC(CO)C1CCCCC1
Reaction #56778
tert-butyl 1-cyclohexyl-2-hydroxyethylcarbamate
收率 66.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
OC1(C(CN2CCNCC2)c2cccc(Cl)c2)CCCCC1
Reaction #57081
1-[1-(3-chlorophenyl)-2-piperazin-1-ylethyl]cyclohexanol
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)NC1CCN(CC(c2ccc(Cl)c(Cl)c2)C2(O)CCCCC2)CC1
Reaction #57084
tert-butyl {1-[2-(3,4-dichlorophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperidin-4-yl}carbamate
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)N1CCN(CC(c2cccc(Br)c2)C2(O)CCCCC2)CC1
Reaction #57093
tert-butyl 4-[2-(3-bromophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylate
收率 98.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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