Zeng-Rong Wong
zengrongwong.bsky.social
Zeng-Rong Wong
@zengrongwong.bsky.social
Singaporean chemist in Canada. Organic and organometallic chemistry.

Currently postdoc fellow @Crudden group at @Queen's University. Previously PhD @Toste Group in @UCB
Do they identify the compounds by comparison of the fragmentation patterns with a database?
March 28, 2025 at 1:19 PM
Any nucleophilic substitution catalyst should fit, e.g. proteases which are important for digestion of proteins in the digestive system or for meat tenderisation.
February 10, 2025 at 7:36 PM
The confusion arises from 'catalyst' being used in two different ways:

1) Basic textbook definitions: enabling elementary step of specific substrate X --> specific product Y (e.g. a specific stereoisomer)

2) Favouring one of multiple products (Y, Y', Y''...) that can be formed from X
February 6, 2025 at 5:59 PM
'Stereoselective catalysis' is making a statement about 4 reaction rates, that the rate of formation of a R-stereocenter, k_cat(R) is larger than any of k_cat(S), k_uncat(R), k_uncat(S)
February 6, 2025 at 5:52 PM
Catalysis refers to a specific elementary step that produces a specific product (e.g. an enantiomer). E.g. reduction to form a (+)-alcohol can be catalyzed by an enzyme, but that doesn't necessarily imply anything about the k_cat/k_uncat for formation of the (-)-alcohol or any racemization process.
February 6, 2025 at 5:45 PM
Hi, my Google Scholar profile is at scholar.google.com/citations?us....

Thanks!
January 28, 2025 at 3:30 PM