ethanol n-hexane

C[C@]1(c2cc(Br)ccc2F)CO1
Reaction #67508
(S)-2-(5-Bromo-2-fluoro-phenyl)-2-methyl-oxirane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CC(C)(C)c1[nH]cnc1/C=C1\NC(=O)[C@@H](Cc2ccccc2)NC1=O
Reaction #78915
(+)-phenylahistin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCS(=O)(=O)N=C(NC)NCCSCc1[nH]cnc1C
Reaction #94226
N-methyl-N'-[2-((4-methyl-5-imidazolyl)methylthio)ethyl]-N"-n-propanesulphonylguanidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
C[C@]1(c2cc(Br)ccc2F)CO1
Reaction #168755
(S)-2-(5-Bromo-2-fluoro-phenyl)-2-methyl-oxirane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[C@]1(c2cc(Br)ccc2F)CO1
Reaction #308908
(S)-2-(5-Bromo-2-fluoro-phenyl)-2-methyl-oxirane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
N[C@@H](CCO)c1ccc(C(F)(F)F)nc1
Reaction #329044
(S)-3-amino-3-(6-(trifluoromethyl)pyridin-3-yl)propan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=CC(C)(C)c1[nH]cnc1/C=C1\NC(=O)[C@@H](Cc2ccccc2)NC1=O
Reaction #364920
(+)-phenylahistin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCn1nccc1[C@@H]1CCC[C@H]1O
Reaction #425101
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cn1nccc1[C@@H]1CCC[C@H]1O
Reaction #425121
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cn1nccc1[C@@H]1CCCC[C@H]1O
Reaction #425140
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O[C@H]1CCCC[C@@H]1c1cn[nH]c1
Reaction #425218
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(=O)NCC[C@@H]1CCc2ccc3nc(C)sc3c21
Reaction #427894
title compound
수율 50.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(=O)NCC[C@H]1CCc2ccc3nc(C)sc3c21
Reaction #427895
title compound
수율 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCCc1cc(=O)oc2c3c(c4c(c12)OC(C)(C)C=C4)OC(C)C(C)C3O
Reaction #429993
calanolide A
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CN[C@H]1Cc2ccccc2[C@H]1Cc1ccc(Cl)c(Cl)c1
Reaction #431102
(±)cis-1-(3,4-Dichlorobenzyl)-2-methylaminoindane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=C1C2CCCCC2=Nc2ccccc2N1Cc1ccccc1
Reaction #443325
titled compound
수율 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CCCc1cc(=O)oc2c3c(c4c(c12)OC(C)(C)C=C4)OC(C)C(C)C3O
Reaction #444866
calanolide A
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CCCc1cc(=O)oc2c3c(c4c(c12)OC(C)(C)C=C4)OC(C)C(C)C3O
Reaction #449407
calanolide A
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CCCc1cc(=O)oc2c3c(c4c(c12)OC(C)(C)C=C4)OC(C)C(C)C3O
Reaction #450442
calanolide A
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CCCc1cc(=O)oc2c3c(c4c(c12)OC(C)(C)C=C4)OC(C)C(C)C3O
Reaction #451015
calanolide A
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
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