✦ LIBER ✦

Mixed metal base LICKOR as key reagent in the synthesis of conjugate alkadien-1-ols. A new route to an insect attractant

✍ Scribed by Fulvio Cominetti; Annamaria Deagostino; Cristina Prandi; Paolo Venturello

Book ID: 104208943
Publisher: Elsevier Science
Year: 1998
Tongue: French
Weight: 337 KB
Volume: 54
Category: Article
ISSN: 0040-4020
DOI: 10.1016/s0040-4020(98)00918-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Mixed Metal Base LI

ChemInform Abstract: Mixed Metal Base LICKOR as Key Reagent in the Synthesis of Conjugate Alkadien-1-ols. A New Route to an Insect Attractant.

✍ Fulvio Cominetti; Annamaria Deagostino; Cristina Prandi; Paolo Venturello 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

Mixed Metal Base LICKOR as Key Reagent in the Synthesis of Conjugate Alkadien-1-ols. A New Route to an Insect Attractant. -Studies of the reactivity of 2-alkenyltetrahydrofurans with the LICKOR super base show that it promotes 1,4-eliminative ring fission affording conjugate alkadien-1-ols with hig

Mixed Superbase LICKOR as a Key Reagent

Mixed Superbase LICKOR as a Key Reagent for the Synthesis of Conjugate Dienes from Citral and Farnesal – A New Route to a Potential Mimic Agent of Juvenile Hormones by Diels–Alder Cycloaddition

✍ Paolo Balma Tivola; Annamaria Deagostino; Claudia Fenoglio; Mariella Mella; Cris 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 148 KB 👁 2 views

Treatment of the dimethyl acetals of citral (1) and farnesal be subjected to a Diels-Alder reaction, which allows further synthetic elaboration. In particular, in the case of farnesal (2) with the superbase "LICKOR" in THF at low temperatures induces regioselective metallation at the allylic methyl