113789-82-5Relevant academic research and scientific papers
A Tandem Oxidation-Intramolecular Diels-Alder Reaction
Wu, Hsien-Jen,Pan, Kai
, p. 898 - 900 (1987)
Oxidation of the furan (4) with pyridinium chlorochromate gave the intramolecular Diels-Alder cycloadduct (6) as the major product, presumably via the intermediate.
Iodine-induced cyclization reaction of endo-thioester substituted norbornenes followed by methylthio group rearrangement
Wu, Hsien-Jen,Tsai, Shih-Hwa,Chung, Wen-Sheng
, p. 8209 - 8212 (1996)
Treatment of the endo-thioester group substituted norbornenes 3a-3d with iodine in aqueous tetrahydrofuran at 25°C gave the novel methylthio group rearranged lactonization products 4a-4d in 80% yields; iodolactonization reaction of 9 was applied to the synthesis of novel diacetal trioxa-cage compound 13.
Novel Heterocyclic Cage Compounds from 2-Methylthiofurans
Wu, Hsien-Jen,Huang, Fang-Jung,Lin, Chu-Chung
, p. 770 - 771 (2007/10/02)
Some novel heterocyclic cage compounds 1a-1c were synthesized from the corresponding 2-methylthiofurans 2a-2c in a short sequence.
