4.6 Article

Studies on a catalytic version of the Matteson asymmetric homologation reaction

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 19, Issue 19, Pages 4279-4284

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ob00604e

Keywords

-

Funding

  1. Cardiff University
  2. Government of Saudi Arabia
  3. Government of Iraq
  4. King Saud University

Ask authors/readers for more resources

Studies have shown that a chiral catalytic system based on a mannitol derivative in the catalytic asymmetric version of the Matteson reaction provides substantial asymmetric induction similar to that achieved with a bis(oxazoline) derivative and ytterbium triflate. Additionally, it was found that fresh ytterbium triflate may reduce the level of asymmetric induction, while aged ytterbium triflate or a fresh sample treated with water can improve the induction effect.
Studies of a catalytic asymmetric version of the Matteson reaction between dichloromethylboronates and organolithium reagents have been undertaken. From several different chiral catalytic systems studied, only one based on a mannitol derivative has given substantial asymmetric induction close to that previously achieved with a bis(oxazoline) derivative and ytterbium triflate. More detailed study of the latter reaction revealed that fresh ytterbium triflate actually reduced the level of asymmetric induction, while aged ytterbium triflate, or a fresh sample that had been treated with water, brought about improved induction. The implications of these findings are discussed.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available