✦ LIBER ✦

Nitro ylides. 7. Synthesis and some reactions of alkyl-substituted selenonium nitro ylides

✍ Scribed by V. V. Semenov; L. G. Mel'nikova; S. A. Shevelev; A. A. Fainzil'berg

Book ID: 112443818
Publisher: Springer
Year: 1980
Tongue: English
Weight: 646 KB
Volume: 29
Category: Article
ISSN: 1573-9171
DOI: 10.1007/bf00951893

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of Spirooxindolo/Spiroindano N

Synthesis of Spirooxindolo/Spiroindano Nitro Pyrrolizidines through Regioselective Azomethine Ylide Cycloaddition Reaction

✍ Poornachandran, Mahalingam; Raghunathan, Ragavachary 📂 Article 📅 2007 🏛 Taylor and Francis Group 🌐 English ⚖ 204 KB

ChemInform Abstract: Synthesis of Spiroo

ChemInform Abstract: Synthesis of Spirooxindolo/Spiroindano Nitro Pyrrolizidines Through Regioselective Azomethine Ylide Cycloaddition Reaction.

✍ Mahalingam Poornachandran; Ragavachary Raghunathan 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 21 KB 👁 2 views

Synthesis and reactions of substituted n

Synthesis and reactions of substituted nitro-allylating reagents

✍ Paul Knochel; Dieter Seebach 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 212 KB

Microwave-Assisted Wittig Reaction of Se

Microwave-Assisted Wittig Reaction of Semistabilized Nitro-Substituted Benzyltriphenyl-Phosphorous Ylides with Aldehydes in Phase-Transfer Conditions

✍ Rodrigues, Tiago; Lopes, Francisca; Moreira, Rui 📂 Article 📅 2011 🏛 Taylor and Francis Group 🌐 English ⚖ 225 KB

Synthesis of isoxazoline-N-oxides by the

Synthesis of isoxazoline-N-oxides by the reaction of sulfonium ylides withα,β-unsaturated nitro compounds

✍ A. V. Samet; A. M. Shestopalov; V. V. Semenov 📂 Article 📅 1996 🏛 Springer US 🌐 English ⚖ 94 KB

Synthesis of Highly Functionalized Stabl

Synthesis of Highly Functionalized Stable Heterocyclic Phosphorus Ylides. Cycloaddition Reaction between Conjugated Phosphorus Ylides and Alkyl Propiolates

✍ Issa Yavari; Farahnaz Nourmohammadian 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 83 KB

AbstractÐProtonation of the reactive 1:1 intermediates produced in the reaction between triphenylphosphine and dialkyl acetylenedicarboxylates by 3-chlorotetrahydrofuran-2,4-dione leads to vinylphosphonium salts, which undergo Michael addition with the conjugate base of the CH-acid to produce highly