65399-15-7Relevant articles and documents
REACTION OF 3a,4-DIHYDROPHTHALIDES WITH ACETYLENIC DIENOPHILES
Noguchi, Michihiko,Kakimoto, Shinji,Kajigaeshi, Shoji
, p. 665 - 668 (2007/10/02)
The tricycloocta-2,5-diene-4,7-carbolactones, the initially-formed Diels-Alder adducts from 3a,4-dihydrophthalides and acetylenic dienophiles, were so strained that they underwent the retro-Diels-Alder reaction to afford the benzene derivatives in good yields.