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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†

✍ Scribed by Alcaide, Benito; Almendros, Pedro; Aragoncillo, Cristina

Book ID: 111951845
Publisher: American Chemical Society
Year: 2001
Tongue: English
Weight: 141 KB
Volume: 66
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo005715z

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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

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Diastereoselective

ChemInform Abstract: Diastereoselective Baylis—Hillman Reaction of 4-Oxoazetidine-2-carbaldehydes: Rapid, Stereocontrolled and Divergent Radical Synthesis of Highly Functionalized β-Lactams Fused to Medium Rings.

✍ Benito Alcaide; Pedro Almendros; Cristina Aragoncillo 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views