## Abstract A series of __cis__‐α,γ‐difunctionalized five‐membered cyclic β‐oxo esters have been chemo‐, regio‐ and diastereoselectively prepared through an efficient domino anionic ring‐cleavage/ring‐reconstitution/alkylation sequence including a 1,3‐shift of the ester group. These unsaturated sub
Synthesis of Bridged Bicyclic Molecules using Halocarbenes. Derivatives of bicyclo[4.2.1]nonane
✍ Scribed by Charles W. Jefford; Ulrich Burger; François Delay
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- German
- Weight
- 847 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The addition of dichlorocarbene (generated by the interaction of sodium methoxide and ethyl trichloroacetate) to bicyclo[3.2.1]oct‐2‐ene, its 3‐chloro and exo‐3,4‐dichloro derivatives gives the exo 1 : 1 adducts in yields of 94, 89 and 48%. By suitable chemical reactions of these adducts, convenient syntheses of bicyclo[4.2.1]nona‐2,4‐diene and bicyclo[4.2.1]non‐3‐ene, together with their monochloro, dichloro and trichloro derivatives are obtained. Bicyclo[4.2.1]‐nonan‐3‐one is also obtained from bicyclo[4.2.1]non‐3‐ene in a synthesis starting from the readily available 5‐hydroxymethylnorborn‐2‐ene in an overall yield of 20%.
📜 SIMILAR VOLUMES
## Abstract __N__‐Cyanolactam 2‐imines 1 are versatile NCNC building blocks for the synthesis of partially saturated bicyclic compounds. Reactions with acidic methyl halides, hydroxylamine __O__‐sulfonic acid, and phenyl isocyanate afford bicyclic imidazole (4), 1,2,4‐triazole (6), and 1,3,5‐tri