class="bi x0 y0 w0 h1"
class="bi x0 y0 w0 h1"
class="bi x0 y0 w1 h2"
class="bi x0 y0 w0 h1"
class="bi x0 y0 w2 h4"
class="bi x0 y0 w4 h6"
4. J. S. Brimacombe and L.C. N. Tuker - Reaction
of
D-glycero-D-glulo-heptono-y-Iactone
with acetone, Carbohydrate Research 2 (1966) 341-348.
5. Tonny
K. M. Shing, Hon-chung Tsui, Zhao-hui Zhou
~nd
Thomas
C.
W.
Mak -
Stereose1ective -syntheses od 2,4:5,6-Di-O-isopropylidene-I-C-phenyl-D-glycero-D-ido-
hexitol and 2,4:5,6-Di-O-isopropylidene-I-C-phenyl-D-glycero-D-gulo-hexitol from
D-
glycero-D-gulo-heptono-y-Iactone. X-ray Structure
of
I-O-Acetyl-2,4: 5,6-Di-O-
isopropylidene-I-C-phenyl-D-glycero-D-ido-hexitol, J. Chern. Soc. Perkin Trans 1 (1992)
887-893.
6. Masayoshi Tsubuki, Kazuo Kanai, Hiromasa Nagase, and Toshio Honda -
Stereocontrolled Syntheses
of
Novel Styryl Lactones, (+)-Goniodiol, (+)-Goniotriol, (+)-
8-Acetylgoniotriol, (+ )-Goniofufurone, (+ )-9-Deoxygoniopypyrone, (+ )-Gonipypyrone,
and (+ )-Altholactone from Common Intermediates and Cytotoxicity

of
howiinol and intermediate
products were estabilished by MS and
NMR
spectroscopies.
Dia
chi:
Nh(in hili
ngay
15 tJuing 2 niim
2008
Vi~n
H6a
hQc,
Vi~n
KH&CNVN.
89