78508-88-0Relevant articles and documents
A facile solid-phase synthesis of substituted 2(5H)-furanones with sulfone traceless linker
Sheng, Shou-Ri,Huang, Pei-Gang,Zhou, Wei,Luo, Hai-Rong,Lin, Shu-Ying,Liu, Xiao-Ling
, p. 2603 - 2605 (2007/10/03)
A novel solid-phase synthetic method for substituted 2(5H)-furanones with traceless sulfone linker strategy has been developed. The products were obtained in good yields and excellent purities.
STUDIES ON STRUCTURALLY SIMPLE α,β-BUTENOLIDES. III. BEHAVIOUR OF (-)-(S)-δ-HETEROSUBSTITUTED γ-METHYL-α,β-BUTENOLIDES TOWARDS NUCLEOPHILES. PROTOANEMONIN AS INTERMEDIATE IN AN ELIMINATION-ADDITION MECHANISM.
Camps, P.,Cardellach, J.,Corbera, J.,Font, J.,Ortuno, R. M.,Ponsati, O.
, p. 395 - 400 (2007/10/02)
The reactivity of the title compounds with different nucleophiles has been checked and it was shown that products from reaction with sodium phenylthiolate result from an elimination-addition process in which protoanemonin is the key intermediate.The synthesis of (-)-(R)-β-angelica lactone is reported for the first time.
NEW SYNTHETIC ENTRIES TO γ-HETEROMETHYL-SUBSTITUTED α,β-BUTENOLIDES
Estopa, C.,Font, J.,Moreno-Manas, M.,Sanchez-Ferrando, F.,Valle, S.,Vilamajo, L.
, p. 1467 - 1470 (2007/10/02)
The title compounds have been obtained from C3 plus C2 synthons by a variety of chemical and photochemical methods.
