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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

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