𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselectivity of Macrocyclic Ring-Closing Olefin Metathesis

✍ Scribed by Lee, Choon Woo; Grubbs, Robert H.


Book ID
126082724
Publisher
American Chemical Society
Year
2000
Tongue
English
Weight
7 KB
Volume
2
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Synthesis of macrocyclic lactams and lac
✍ William P.D. Goldring; AndrΓ©S. Hodder; Larry Weiler πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 254 KB

## A&Wrack Lactones and lactams 4-6 were synthesized from a series of acyclic dienes 1-3 via ringclosing olefin metathesis, as shown in equation 1. The geometry of the resulting double bond was determined, and the UZratios compared to values from molecular mechanics calculations.

Enamideβˆ’Olefin Ring-Closing Metathesis
✍ Kinderman, Sape S.; van Maarseveen, Jan H.; Schoemaker, Hans E.; Hiemstra, Henk; πŸ“‚ Article πŸ“… 2001 πŸ› American Chemical Society 🌐 English βš– 125 KB
Synthesis of Macrocyclic Carbonates with
✍ Anna Michrowska; Piotr Wawrzyniak; Karol Grela πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 97 KB πŸ‘ 1 views

## Abstract This study shows the efficiency of modern well‐defined ruthenium catalysts for the formation of musk‐odored macrocyclic carbonates with ring sizes between 15βˆ’23 atoms. It also reveals that, in these cases, geometric factors are very important and that smaller ring carbonates are difficu