𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: A Concise Asymmetric Synthesis of the Pheromone 1-Methylcyclohex-2- enol (IV) via a “Merged Substitution-Elimination Reaction”.

✍ Scribed by D. P. G. HAMON; K. L. TUCK

Publisher
John Wiley and Sons
Year
2010
Weight
30 KB
Volume
28
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

✦ Synopsis

A

Concise Asymmetric Synthesis of the Pheromone 1-Methylcyclohex-2-enol (IV) via a "Merged Substitution-Elimination Reaction".

-The title compound (III) is prepared from cyclohexene (I) via Sharpless asymmetric dihydroxylation using AD-mix-β, tosylation and an unexpected elimination reaction. -(HAMON, D.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Direct and Genera
ChemInform Abstract: A Direct and General Synthesis of 5-Substituted 3-Trifluoromethyl-1,2,4-triazoles via the Three Component Condensation Reaction of Ethyl Trifluoroacetate, Hydrazine and Amidines.
✍ Kazumasa Funabiki; Naoko Noma; Gouhaku Kuzuya; Masaki Matsui; Katsuyoshi Shibata 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

A Direct and General Synthesis of 5-Substituted 3-Trifluoromethyl-1,2,4-triazoles via the Three Component Condensation Reaction of Ethyl Trifluoroacetate, Hydrazine and Amidines. -Because of their potent biological and physiological activities a general and practicable one-pot reaction to 5-substit