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Straightforward Asymmetric Entry to Highly Functionalized 3-Substituted 3-Hydroxy-β-lactams via Baylis—Hillman or Bromoallylation Reactions.

✍ Scribed by Benito Alcaide; Pedro Almendros; Cristina Aragoncillo; Raquel Rodriguez-Acebes

Book ID
101957035
Publisher
John Wiley and Sons
Year
2004
Weight
189 KB
Volume
35
Category
Article
ISSN
0931-7597

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📜 SIMILAR VOLUMES

Asymmetric synthesis of densely function
Asymmetric synthesis of densely functionalized 3-substituted 3-hydroxy-β-lactams via novel, highly stereoselective Baylis-Hillman and allylation reactions of enantiopure 3-oxo-2-azetidinones
✍ Benito Alcaide; Pedro Almendros; Cristina Aragoncillo 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 238 KB

New asymmetric routes based on both Baylis-Hillman and allylation reactions of enantiopure 3-oxo-2azetidinones are used for the highly stereoselective, efficient preparation of densely functionalized 3-substituted 3-hydroxy-l~-lactams.

ChemInform Abstract: Straightforward Asy
ChemInform Abstract: Straightforward Asymmetric Entry to Highly Functionalized Medium-Sized Rings Fused to β-Lactams via Chemo- and Stereocontrolled Divergent Radical Cyclization of Baylis—Hillman Adducts Derived from 4-Oxoazetidine-2-carbaldehydes.
✍ Benito Alcaide; Pedro Almendros; Cristina Aragoncillo 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 41 KB 👁 1 views

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