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synlett 17/2009 - Thieme Chemistry

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Letters<br />

X Table of Contents<br />

2831 Y. Yue<br />

H. Yamamoto<br />

M. Yamane*<br />

2836 J. Clayden*<br />

J. Clayton<br />

R. A. Harvey<br />

O. Karlubíková<br />

2839 R. K. Gessner<br />

K. Chibale*<br />

2844 I. González<br />

A. Pla-Quintana<br />

A. Roglans*<br />

Rhodium-Catalyzed Homocoupling of (1-Acyloxyvinyl)silanes: Synthesis of<br />

1,3-Diene-2,3-diyl Diesters and Their Derivatives<br />

OCOR<br />

SiMe3<br />

2<br />

R1 5 mol%<br />

[RhCl(CO)2]2<br />

Cl3CCOCCl3 toluene, 80 °C<br />

OCOR2 R1 OCOR2 R1 R1 = aryl, alkyl R2 = Me, Ph, OEt, etc. 18–92%<br />

R1 R1 MeO OMe<br />

O<br />

R1 = Ph(CH2) 2 R2 K2CO3 MeOH<br />

= Ph 87%<br />

A One-Pot Synthesis of 2-Aryl-4,5-anti-diphenyloxazolines<br />

O<br />

Cl<br />

R<br />

Ph Ph<br />

(S) (R)<br />

HO<br />

NH2<br />

Et 3N (4 equiv),<br />

CH 2Cl 2, 0–25 °C<br />

HO<br />

O<br />

Ph<br />

NH<br />

R<br />

Ph<br />

MeSO 2Cl,<br />

0–25 °C<br />

Ph<br />

O<br />

N<br />

R<br />

Ph<br />

(R) (R)<br />

13 examples<br />

20–90% yield<br />

A New and Simple Synthesis of Sulfonyl Ureas from Sulfonamides and<br />

N-Alkyl-1,2,4-dithiazolidine-3,5-diones<br />

S<br />

S<br />

O<br />

O<br />

NH<br />

Br R 1<br />

NaHCO3, MeCN<br />

20 °C, 16 h<br />

S<br />

S<br />

O<br />

O<br />

N<br />

R 1<br />

O O<br />

H2N S R 2<br />

Ph3P, K2CO3<br />

PhMe, reflux, 24 h<br />

O O<br />

R<br />

S<br />

N<br />

H<br />

2<br />

Rhodium N-Heterocyclic Carbene Complexes as Effective Catalysts for<br />

[2+2+2]-Cycloaddition Reactions<br />

R<br />

N<br />

Cl<br />

N R<br />

Rh<br />

R = i-Pr, Mes<br />

O<br />

N<br />

H<br />

R 1

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