83988-54-9Relevant articles and documents
Useful Synthetic Routes to Pure exo-5-Vinyl-2-norbornene and endo-5-Vinyl-2-norbornene
Inoue, Yoshiharu
, p. 1954 - 1956 (2007/10/02)
Hydroboration of 5-vinyl-2-norbornene (1) with 9-BBN mainly affords 5-(2-hydroxyethyl)-2- norbornene (2).The iodo ether cyclization of 2 can convert only endo-5-(2-hydroxyethyl)-2-norbornene (2b) to iodo ether 10, followed by reductive elimination and subsequent dehydration to furnish endo-5-vinyl-2-norbornene (1b) which has not been isolated in pure form.Meanwhile, unreacted exo-5-(2-hydroxyethyl)-2-norbornene (2a) produces exo-5-vinyl-2-norbornene (1a) via dehydration.
Acid-catalysed Lactonisation and Iodolactonisation of Norbornene-carboxylic Acids
Sadikun, Amirin bin,Davies, David I.
, p. 2461 - 2466 (2007/10/02)
The acid-catalysed lactonisation of 3-(norborn-5-en-2-yl)propionic acid and 4-(norborn-5-en-2-yl)butyric acid affords 3-(2-exo-hydroxynorborn-2-endo-yl)propionic acid spiro-γ-lactone and 4-(2-exo-hydroxynorborn-2-endo-yl)butyric acid spiro-δ-lactone, resp