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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