I am thrilled to share that I will be joining the outstanding Department of Chemistry at Indiana University Bloomington as an Assistant Professor starting January 2026!
03.04.2025 03:24 β π 65 π 6 π¬ 6 π 1
Do they identify the compounds by comparison of the fragmentation patterns with a database?
28.03.2025 13:19 β π 0 π 0 π¬ 1 π 0
23.02.2025 21:07 β π 40 π 2 π¬ 0 π 1
Any nucleophilic substitution catalyst should fit, e.g. proteases which are important for digestion of proteins in the digestive system or for meat tenderisation.
10.02.2025 19:36 β π 0 π 0 π¬ 0 π 0
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
06.02.2025 17:59 β π 0 π 0 π¬ 0 π 0
'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)
06.02.2025 17:52 β π 0 π 0 π¬ 1 π 0
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.
06.02.2025 17:45 β π 0 π 0 π¬ 1 π 0
Hi, my Google Scholar profile is at scholar.google.com/citations?us....
Thanks!
28.01.2025 15:29 β π 0 π 0 π¬ 0 π 0
Hi, itβs me. Iβm the problem, itβs me.
27.01.2025 00:25 β π 36 π 6 π¬ 0 π 0
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