A new entry to α-alkylidene-β-lactams by 4-exo-dig cyclization of carbamoyl radicals
✍ Scribed by Shin-ichi Fujiwara; Yoshihiko Shimizu; Yuji Imahori; Masashi Toyofuku; Tsutomu Shin-ike; Nobuaki Kambe
- Book ID
- 104096432
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 285 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
An efficient synthesis of pentacyclic b-lactams has been achieved in high yield via a novel 6-exo-trig, 7-endo-dig tandem radical cyclization.
A Novel Entry to 5a-Carba-hexopyranoses from Carbohydrates Based on a 6-exo-dig Radical Cyclization: Synthesis of 5a-Carbaβ-D-mannopyranose Pentaacetate. -Mannose-derived diacetonide (VI) undergoes a 6-exo-dig radical cyclization to give highly functionalized cyclohexanes which are correlated with
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