✦ LIBER ✦

Oxidation of 1-hydroxyazetidines to four-membered cyclic nitrones and β-lactams

✍ Scribed by P. A. van Elburg; D. N. Reinhoudt

Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 868 KB
Volume: 107
Category: Article
ISSN: 0165-0513
DOI: 10.1002/recl.19881070505

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Oxidation of N-hydroxyazetidines: A nove

Oxidation of N-hydroxyazetidines: A novel synthesis of N-acetoxy β-Lactams and four-membered cyclic nitrones

✍ M.L.M. Pennings; D.N. Reinhoudt 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 228 KB

ChemInform Abstract: 1,3-Dipolar Cycload

ChemInform Abstract: 1,3-Dipolar Cycloadditions of Five and Six Membered Cyclic Nitrones to α,β-Unsaturated Acid Derivatives

✍ Pedro de March; Marta Figueredo; Josep Font 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

Straightforward Synthesis of Diverse 1-D

Straightforward Synthesis of Diverse 1-Deoxyazapyranosides via Stereocontrolled Nucleophilic Additions to Six-Membered Cyclic Nitrones

✍ Ting-Hao Chan; Yi-Fan Chang; Jung-Jung Hsu; Wei-Chieh Cheng 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 250 KB

ChemInform Abstract: Regioselective Tran

ChemInform Abstract: Regioselective Transformation of O-Propargylic Arylaldoximines to Four-Membered Cyclic Nitrones by Copper-Catalyzed Skeletal Rearrangement.

✍ Itaru Nakamura; Toshiharu Araki; Dong Zhang; Yu Kudo; Eunsang Kwon; Masahiro Ter 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 45 KB 👁 1 views

Chemistry of 4-membered cyclic nitrones

Chemistry of 4-membered cyclic nitrones (2, 3-dihydroazete 1-oxides); a novel one-step synthesis of N-acetoxy β-latams

✍ M.L.M. Pennings; D.N. Reinhoudt 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 236 KB

1, 3-Cycloadditions to Highly Substitute

1, 3-Cycloadditions to Highly Substituted, Strained Double Bonds: Spiro β-lactams from α-methylidene-β-lactams by reactions with diphenylnitrilimine, acetonitrile oxide, nitrones, and diazomethane

✍ Arthur Strauss; Hans-Hartwig Otto 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 German ⚖ 558 KB

## Abstract Substituted dihydropyrazole‐spiro‐β‐lactams and isoxazolidine‐spiro‐β‐lactam derivatives are regio‐ and stereoselectively prepared by 1, 3‐cydoadditions between substituted α‐methylidene‐β‐lactams and diazomethane, nitrones, or the __in__‐__situ__‐prepared dipoles ‘diphenylnitrilimine’