✦ LIBER ✦

Inverse electron demand diels-alder reactions of indole IV. A new route to β-carbolines

✍ Scribed by Wen-Hong Fan; Mamta Parikh; John K. Snyder

Publisher: Elsevier Science
Year: 1995
Tongue: French
Weight: 428 KB
Volume: 36
Category: Article
ISSN: 0040-4039
DOI: 10.1016/00404-0399(50)1347-k

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Inverse electron demand Diels-Alder reac

Inverse electron demand Diels-Alder reactions of indole. VI. A fully removable tether for intramolecular reactions with 1,2,4-triazines

✍ Zhao-Kui Wan; John K Snyder 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 267 KB

Intramolecular Inverse-Electron-Demand D

Intramolecular Inverse-Electron-Demand Diels—Alder Reactions of Imidazoles with 1,2,4-Triazines: A New Route to 1,2,3,4-Tetrahydro-1,5-naphthyridines and Related Heterocycles.

✍ Brian R. Lahue; Sie-Mun Lo; Zhao-Kui Wan; Grace H. C. Woo; John K. Snyder 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 39 KB 👁 2 views

ChemInform Abstract: Inverse Electron De

ChemInform Abstract: Inverse Electron Demand Diels—Alder Reactions of Indole. Part 6. A Fully Removable Tether for Intramolecular Reactions with 1,2,4-Triazines.

✍ Z.-K. WAN; J. K. SNYDER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

ChemInform Abstract: Inverse Electron De

ChemInform Abstract: Inverse Electron Demand Diels—Alder Reaction — A Facile Synthetic Route to Pyrazoles from Conjugated Oximes Utilizing Diimides as Dipolarophile.

✍ Shahadat Ahmed; Moanochet Longchar; Romesh C. Boruah 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

Tandem ‘inverse electron-demand’ Diels-A

Tandem ‘inverse electron-demand’ Diels-Alder reactions of dienamines with a 1,2,4,5-tetrazine. A new azo-bridged ring system

✍ András Kotschy; David M. Smith; Attila Cs. Bényei 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 234 KB

Regiospecific Inverse-Electron-Demand Di

Regiospecific Inverse-Electron-Demand Diels–Alder Reaction of Simultaneously Electrogenerated Diene and Dienophile: An Expeditious Route to Polyfunctionalized 1,4-Benzoxazine Derivatives

✍ Martine Largeron; Anne Neudorffer; Marc Vuilhorgne; Estelle Blattes; Maurice-Ber 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 112 KB

Quinonoid systems are powerful intermediates for organic synthesis and constitute potential precursors to numerous naturally occurring substances. However, the synthesis of quinonoid entities, particularly o-quinones and o-azaquinones, which are usually unstable and very prone to polymerization, is