ID Name Structure References (top 5) Molecular Target(s)
1ID:20
ACETAL


NSC#:227930
Aldrich#:176958
Aldrich#:81890
Properties
C7H16O2    132.2





1:  Guindon Y, Ogilvie WW, Bordeleau J, Cui WL, Durkin K, Gorys V, Juteau H, Lemieux R, Liotta D, Simoneau B, Yoakim C.
Opening of Tartrate Acetals Using Dialkylboron Bromide: Evidence for Stereoselectivity Downstream from Ring Fission.
J Am Chem Soc.    impact factor:   5.537
2003;  125(2): 428-436

2:  Valahovic MT, Gunnoe TB, Sabat M, Harman WD.
Ligand-modulated stereo- and regioselective tandem addition reactions of rhenium-bound naphthalene.
J Am Chem Soc.    impact factor:   5.537
2002;  124(13): 3309-15

3:  Murahashi S, Imada Y, Kawakami T, Harada K, Yonemushi Y, Tomita N.
Enantioselective addition of ketene silyl acetals to nitrones catalyzed by chiral titanium complexes. Synthesis of optically active beta-amino acids.
J Am Chem Soc.    impact factor:   5.537
2002;  124(12): 2888-9

4:  Kim S, Lim CJ, Song C, Chung WJ.
Novel radical alkylation of carboxylic imides.
J Am Chem Soc.    impact factor:   5.537
2002;  124(48): 14306-7

5:  Powell SA, Tenenbaum JM, Woerpel KA.
Utilization of 1-oxa-2,2-(dimesityl)silacyclopentane acetals in the stereoselective synthesis of polyols.
J Am Chem Soc.    impact factor:   5.537
2002;  124(43): 12648-9

ALK
ARG
C-AMP
EGFR-1
EGFR-2
FGF-2
HCK
HGF
KIT
LC
MER
MET
NADPH CYTOCHROME P450
NM-23
P21
P450
SAP
STEP
SRC
THYMIDYLATE SYNTHASE
THYMIDYLATE SYNTHETASE
PKC
 
Time used: 250 milliseconds.

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