The phrase "addition schemes" is correct and usable in written English.
It can be used in contexts related to mathematics, finance, or any field where different methods or plans for adding or combining elements are discussed.
Example: "The study explored various addition schemes to improve the efficiency of the budgeting process."
Alternatives: "addition methods" or "addition strategies".
The current mechanism considers a detailed set of PAH growth routes, and includes hydrogen atom migration, possible free radical addition schemes, methyl substitution/acetylene addition pathways, cyclopentadienyl moiety in aromatic ring formation, and numerous reactions between aromatic radicals and molecules.
For example, the traditional fully redundant (i.e., the result and both of the operands are represented in a redundant format) and semi-redundant (i.e., the result and only one of the operands are redundant) binary addition schemes have influenced the design and implementation of similar decimal arithmetic units.
In addition, schemes may fail, especially if collection of funds is insufficient to cover costs or default rates are high, or may exclude the poorest individuals.
The use of BEC eliminates the n/4 number of adders, existing in the conventional addition scheme, where n denotes the multiplier input width.
This is followed by the main result, which is the development of a novel, low depth, carry lookahead addition scheme based on threshold logic.
In this proposed mechanism the nucleophilic aromatic substitution reaction occurs via a two-step mechanism in which the first step is the addition Scheme 4 Plausible mechanisms for the synthesis of flunixin.
The substrate addition scheme used was the same in all the SSCF experiments.
Compound 443 was prepared by reaction of phenyl dichlorophosphate with l-alanine isopropyl ester hydrochloride followed by pentafluorophenol addition (Scheme 131).
We formed hydrogels by copolymerizing acrylate-terminated multiarm PEG with a thiol-terminated LPRTG peptide and thiol-terminated multiarm PEG through Michael-type addition (Scheme 1 ) as reported earlier.
In contrast, the biocatalytic analogue to this reaction is a trans-specific addition (Scheme 1). 1, 7, 12, 16, 23 Structurally, OYEs have in common an 8- or TIM-barrel fold, conserved throughout the whole protein family.
The relative configuration of the major product 155 was found to be consistent with the syn-mechanism of the addition (Scheme 41).[ 65] On the other hand, cyclization of the deuteriated acetamide 156 a, carried out in the absence of a strong base, afforded the arylated pyrrolidine derivative 158 (Scheme 42) as a result of an anti-amidopalladation (156 a → 157 a).
