𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of azetidin-3-ones by heterocyclization of α-cyclohexylamino-α′,Β′-epoxy ketones

✍ Scribed by A. M. Zvonok; N. M. Kuz'menok; L. S. Stanishevskii

Publisher
Springer US
Year
1988
Tongue
English
Weight
434 KB
Volume
24
Category
Article
ISSN
0009-3122

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Highly stereoselective synthesis of eryt
Highly stereoselective synthesis of erythro-α, β-epoxy alcohols by the reduction of α, β-epoxy ketones with zinc borohydride
✍ Tadashi Nakata; Tadasu Tanaka; Takeshi Oishi 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 253 KB

Erythro-a, B-epoxy alcohols were prepared in high stereoselectivity by zinc borohydride reduction of the corresponding a, B-epoxy ketones regardless of the substituents on the epoxide ring. Epoxidation of the ally1 alcohols (L) with tert-butyl hydroperoxide catalyzed by VO(acac)2 was reported to giv

Synthesis of α-iodo-α,β-unsaturated keto
Synthesis of α-iodo-α,β-unsaturated ketones by the reaction of α-silyl-α,β-unsaturated ketones with ICl or IClAlCl3
✍ Asaf Alimardanov; Ei-ichi Negishi 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 262 KB

Treatment of c~-silyl-cc,[~-unsaturated enones, readily preparable as regio-and stereodefined compounds in high yields, with either 2 equiv, oflCl or one equiv, each oflC1 and A1C13 provides the corresponding cc-iodo-a,[3unsaturated enones in high yields.