Bis (cyclopentadienyl)titanium dichloride

$C/C(=C\c1csc(C)n1)[C@@H]1C/C=C\CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #71520

epothilone C

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09

$C/C(=C\c1csc(C)n1)[C@@H]1C/C=C\CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #482439

epothilone C

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08

$C/C(=C\c1csc(C)n1)[C@@H]1C/C=C\CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #742261

epothilone C

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12

Reaction #817930

title compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09

Reaction #999989

title compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09

Fc1ccc(CCCn2cccc2)c(F)[c]1[Ti]([c]1c(F)ccc(CCCn2cccc2)c1F)([CH]1C=CC=C1)[CH]1C=CC=C1

Reaction #1061585

orange glassy resin

Выход 37.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_11

Fc1ccc(Cn2cccc2)c(F)[c]1[Ti]([c]1c(F)ccc(Cn2cccc2)c1F)([CH]1C=CC=C1)[CH]1C=CC=C1

Reaction #1061586

orange crystals

Выход 55.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_11

$C/C(=C\c1csc(C)n1)[C@@H]1C/C=C\CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #1248784

epothilone C

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10

$C/C(=C\c1csc(C)n1)[C@@H]1C/C=C\CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #1248785

epothilone C

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10

$C/C(=C\c1csc(C)n1)[C@@H]1C/C=C\CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #1256700

epothilone C

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11

$C/C(=C\c1csc(C)n1)[C@@H]1C/C=C\CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #1332841

epothilone C

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10

$C/C(=C\c1csc(C)n1)[C@@H]1C/C=C\CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #1381652

epothilone C

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07

$C/C(=C\c1csc(C)n1)[C@@H]1C/C=C\CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #1497509

epothilone C

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12

Reaction #1501321

2-isobutyl-6-methyl-1-heptene

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_02

—

Reaction #1829952

compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_08

Reaction #2067191

2,6-dimethyl-2-methoxy-9-isopropylphenylnonane

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_11