lithium diisopropylamide

Cc1c(Cl)cncc1Cl
Reaction #1016
title compound
수율 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#CC1(Cc2ccccc2)CCN(Cc2ccccc2)CC1
Reaction #1935
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCc1cc(Cl)ccn1
Reaction #1945
title compound
수율 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCc1cc(Cl)c(F)cn1
Reaction #1958
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCc1nc(F)c(F)c(F)c1F
Reaction #1966
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)Oc1c(O)c(F)nc(F)c1F
Reaction #1970
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(/C(=C/c2ccc3c(c2)C(c2ccc(C)cc2)=CCC3(C)C)CC(OC)OC)cc1
Reaction #2721
product E
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1OCCCCC1Cc1ccccc1
Reaction #3065
2-benzylcaprolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)[C@H]1COC(=O)N1C(=O)[C@H](Cc1ccccc1)[C@@H](O)c1ccccc1
Reaction #5037
(4S)-3-[(2R)-2-Benzyl-(3R)-3-hydroxy-3-phenylpropionyl]-4-(2-propyl)-oxazolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#Cc1ccc2c(c1)CCCC2(F)c1ccns1
Reaction #6033
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNC(=S)C(C)(C#N)c1ccc(Cl)cc1
Reaction #6036
N-methyl-2-(4-chlorophenyl)-2-cyano-thiopropionamide
수율 31.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C#Cc1cc2c(cc1C)C(C)(C)CCC2(C)C
Reaction #6080
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
[Li][CH2]CCC
Reaction #6380
n-butyllithium
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(C#Cc1ccccc1)c1ccccc1
Reaction #6587
title compound
수율 61.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COCC1N=C(C2(C)C=CC(CC(C)C)=CC2)OC1c1ccccc1
Reaction #6619
2-(1-methyl-4-isobutylphenyl)-4-methoxymethyl-5-phenyl-2-oxazoline
수율 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C#Cc1ccc2c(c1)C(C)(C)CCS2
Reaction #6631
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C#Cc1ccc2c(c1)C(C)(C)CCO2
Reaction #6641
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C#Cc1ccc2c(c1)C(C)(C)CC(C)(C)O2
Reaction #6645
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C#Cc1cc2c(cc1C)OC(C)(C)CC2(C)C
Reaction #6648
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[Si](C)(C)CCOCn1cc(-c2ccc([N+](=O)[O-])cc2)nc1C=O
Reaction #7197
title compound
수율 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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