An enantioselective route to pyrrolidines: Removal of the chiral template from homochiral pyrroloimidazoles
โ Scribed by Raymond CF Jones; Kevin J Howard; John S Snaith
- Book ID
- 103407747
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 222 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
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๐ SIMILAR VOLUMES
The transformation of partially protected aldofuranoses into dienes by Wittig olefination of the anomeric center followed by either allylation or oxopalladation of alkoxy-l,2-propadienes is described. Ring-closing metathesis of the linear dienes gives rise to a variety of highly functionalized and c
An Expeditious Route to the Synthesis of Highly Functionalized Chiral Oxepins from Monosaccharides. -A novel and versatile route to highly functionalized chiral oxepins [cf. (VI) and (IX)] derived from partially protected aldofuranoses such as (I) is reported. The transformation proceeds via Wittig