Accoun ts Letters - Thieme Chemistry
Accoun ts Letters - Thieme Chemistry
Accoun ts Letters - Thieme Chemistry
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<strong>Letters</strong><br />
VIII Table of Conten<strong>ts</strong><br />
1274<br />
A Facile Synthesis of 3’-Deoxy-3’-fluorothymidine<br />
via a Highly Stereoselective Glycosylation with 2,3-<br />
Dideoxy-3-fluoro-D-erythro-pentofuranosyl Diethyl<br />
Phosphite<br />
J. Inagaki, H. Sakamoto, M. Nakajima, S. Nakamura,<br />
S. Hashimoto<br />
1277<br />
Polymer-Supported Acid Catalyst in the Carbon-<br />
Carbon Bond Formation of Acetals with Silylated<br />
Nucleophiles<br />
N. Tanaka, Y. Masaki<br />
1280<br />
Treatment of N-Boc Derivatives of b-Amino Alcohols<br />
with N,N-Diethylaminosulfur Trifluoride Leads to<br />
Chiral Oxazolidinones: An Unexpected Intramolecular<br />
Cyclization<br />
H. Zhao, A. Thurkauf<br />
1283<br />
A New and Extremely Active Corey’s Chiral Oxazaborolidine<br />
Catalyst<br />
K. Ishihara, S. Kondo, H. Yamamoto<br />
1286<br />
Sulfur-Controlled Exo Selective Aryl Radical<br />
Cyclization onto Exo-Methylenecycloalkanes<br />
H. Ishibashi, T. Kobayashi, D. Takamasu<br />
1289<br />
A Novel Carbocyclic Ring Closure of Hex-5enopyranosides<br />
and Pent-4-enofuranosides<br />
J. K. Gallos, T. V. Koftis, A. E. Koumbis, V. I. Mou<strong>ts</strong>os<br />
OTMS<br />
O<br />
N<br />
Me<br />
HN<br />
Me<br />
BzO<br />
O<br />
TMSO N<br />
(1.5 equiv.)<br />
BzO<br />
F<br />
OP(OEt)2 TMSOTf (1.0 equiv.)<br />
EtCN, -50 °C, 30 min<br />
α:β=64:36<br />
R OMe<br />
OMe<br />
(50 mg)<br />
NC<br />
NC<br />
O<br />
O<br />
N<br />
O Ot DAST<br />
CH2F Bu<br />
O<br />
O<br />
O<br />
O<br />
polymer cat. (50 mg), TMS-Nu (1.5 eq.)<br />
CH 3CN, reflux<br />
R = aryl, aliphatic, α,β-unsaturated<br />
Nu = CN, CH2COPh, CH2CO-2-Furyl<br />
N<br />
O Ot CH2OH DAST<br />
Bu<br />
SPh PhS<br />
Br<br />
Bu3SnH AIBN<br />
( )n<br />
( ) n<br />
O<br />
O<br />
N<br />
F<br />
β:α=91:9<br />
R OMe<br />
Nu<br />
N O<br />
O