Journal
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE II FASCICULE C-CHIMIE
Volume 4, Issue 7, Pages 591-598Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/S1387-1609(01)01274-9
Keywords
halolactonization; free radical rearrangement; tri-n-butylstannane; allyltri-n-butylstannane
Categories
Ask authors/readers for more resources
The synthesis of 8-iodooxabicyclo[3.2.1]octanes from substituted benzoic acids via a reductive alkylation-halolactonization sequence is described. These iodolactones were converted to 2-oxabicyclo[3.3.0]octane derivatives upon treatment with either allyltri-n-butylstannane or tri-n-butylstannane via a process that involves a Dowd-Beckwith rearrangement. The scope and limitations of this process are discussed. (C) 2001 Academie des sciences / Editions scientifiques et medicales Elsevier SAS.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available