lithium diisopropylamide mono(tetrahydrofuran)

CCOC(=O)C12CCCN(CCC1)C2
Reaction #5457
product
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)CCCC(=O)/C=C(\O)c1ccc(SC)cc1
Reaction #8180
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C1CCC2(CCN(C(=O)OC(C)(C)C)CC2)C1=O
Reaction #8844
title compound
Yield 110.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC(O)C1CCC2(CCN(C(=O)OC(C)(C)C)CC2)C1=O
Reaction #8846
clear oil
Yield 120.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(O)C1CCC2(CCN(C(=O)OC(C)(C)C)CC2)C1=O
Reaction #8848
clear oil
Yield 479.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cccc2cc(C=O)c(Cl)nc12
Reaction #304035
2-chloro-8-methoxyquinoline-3-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1ccc(S(=O)(=O)n2cc(C=O)c3cc(Br)ccc32)cc1
Reaction #322373
product
Yield 248.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Cc1ccc(S(=O)(=O)NC(=O)C(c2ccc3c(c2)OCO3)c2cn(C)c3cc(C(=O)Cc4ccccn4)ccc23)cc1
Reaction #456537
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1ccc(S(=O)(=O)n2cc(C=O)c3cc(Br)ccc32)cc1
Reaction #463123
product
Yield 248.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
Cc1ccc(S(=O)(=O)n2cc(C=O)c3cc(Br)ccc32)cc1
Reaction #463166
product
Yield 248.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
COc1cccc(CC2CCCCC2(O)c2nc(-c3ccccc3)c(-c3ccccc3)o2)c1
Reaction #464484
2-[(1RS,2RS)-1-hydroxy-2-[(3-methoxyphenyl)methyl]-cyclohexyl]-4,5-diphenyloxazole
Yield 37.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
Cc1ccc(S(=O)(=O)NC(=O)C(c2ccc3c(c2)OCO3)c2cn(C)c3cc(C(=O)Cc4ccccn4)ccc23)cc1
Reaction #468523
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COC(=O)C1(CCCC2COCCO2)CCCC1
Reaction #480637
pale yellow oil
Yield 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
CCOC(=O)C1(COc2ccc3c(c2)CN(C(=O)OC(C)(C)C)CC3)CCN(c2ccncc2)CC1
Reaction #499705
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CCOC(=O)C1(COc2ccc3c(c2)CN(C(=O)OCc2ccccc2)CC3)CCN(C(=O)OC(C)(C)C)CC1
Reaction #499714
title compound
Yield 47.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
C=CCC1(C#N)CCN(C(=O)OC(C)(C)C)CC1
Reaction #499765
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
Cc1ccc(S(=O)(=O)n2cc(C=O)c3cc(Br)ccc32)cc1
Reaction #527605
product
Yield 248.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CCC=C(C=C(OCC)O[Si](C)(C)C)O[Si](C)(C)C
Reaction #592847
1-ethoxy-1,3-bis(trimethylsiloxy)hexa-1,3-diene
Yield 193.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CCC(CC)C(=O)c1ccc(NC(C)=O)cc1
Reaction #626065
N-(4-(2-ethylbutanoyl)phenyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CC(C)(C)OC(=O)CC1COC(=O)C1
Reaction #672746
product
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
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