The phrase "a subsequent reaction" is correct and usable in written English.
It can be used to refer to a reaction that occurs after a previous event or action, often in scientific or analytical contexts.
Example: "After the initial experiment, we observed a subsequent reaction that provided further insights into the chemical process."
Alternatives: "a following reaction" or "a later reaction".
A subsequent reaction converts the products to malonyl-CoA, subsequently diverted to fatty acid synthesis, or methylmalonyl-CoA, which is converted to succinyl-CoA and can enter into the tricarboxylic acid (TCA) cycle (Berg et al, 2002) (Fig 3).
This reaction is a convenient source of the extremely toxic Ni(CO 4, for it can be generated directly in a flask where it is then available to undergo a subsequent reaction.
For example, a proportion of the reactant may be converted into a different product by an alternative process that competes with the desired one; some of the product may undergo a subsequent reaction; or some of the product may be lost in the separation processes required for its isolation in a pure state.
As a subsequent reaction the functionalization of one of the methyl groups to the fluorosulfonyloxymethyl group is found.
The catalyst was extensively washed (with water and then with acetonitrile), dried at 60 °C overnight and reused as such in a subsequent reaction run.
The catalytic performance of these MSN supported metal NPs was tested by aerobic oxidative esterification in a tandem reaction where primary alcohols are oxidized to their corresponding aldehydes and to esters in a subsequent reaction.
Each turn of this cycle (see below The tricarboxylic acid [TCA] cycle) is initiated by the formation of citrate, with six carbon atoms, from oxaloacetate (with four carbons) and acetyl coenzyme A; subsequent reactions result in the reformation of oxaloacetate and the formation of two molecules of carbon dioxide.
CRRL is based on the ability of a hydroquinone to oxidize to a benzoquinone for subsequent reaction with oxyamine-tethered ligands to generate a stable oxime product.
Recently, Ipk1 from C. neoformans (CnIpk1) was identified as an inositol 1,3,4,5,6-pentakisphosphate 2-kinase that catalyzes the phosphorylation of IP5 to form IP6, a substrate for subsequent reaction to produce inositol pyrophosphates, such as PP-IP5/IP7.
In this way, an alcohol, enol or sulfide is converted into a good leaving group for subsequent reaction with an acceptor alcohol.
Likewise, the recent synthesis of the ligand [EuL]H (Fig. 6) relied on attachment of a 1,10-phenanthroline-based sensitizer to c-DTPAA and subsequent reaction of an additional carboxylate with a maleimide derivative [ 17].
