𝔖 Bobbio Scriptorium
✦   LIBER   ✦

π-Facial selectivity of the singlet oxygen [4+2] cycloaddition to chiral naphthalene derivatives: The directing effect of carbon-containing substituents

✍ Scribed by Waldemar Adam; Michael Prein

Book ID
107857677
Publisher
Elsevier Science
Year
1995
Tongue
French
Weight
581 KB
Volume
51
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Substituent effects in the diastereosele
Substituent effects in the diastereoselective [4+2] cycloaddition of chiral naphthalene derivatives with singlet oxygen
✍ Waldemar Adam; Michael Prein 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 382 KB

A bsfracf: From 1 -bromo4-methylnaphthalene eight chiml derivatives 1 with a variety of functional groups at the stereo&e& center were prepcued, which with singlet oxysen led to the corresponding endoperoxides 2 in substituenr-dependent n7facial selectivity of stereoelectronic origin.