The phrase "a moderate yield" is correct and usable in written English.
It can be used in contexts related to finance, agriculture, or any situation where a level of output or return is being discussed.
Example: "The investment strategy resulted in a moderate yield, which was satisfactory given the market conditions."
Alternatives: "a reasonable return" or "a modest output."
The polymerization proceeded well in homogeneous manner to give a moderate yield of polymer.
After screening the reaction conditions (Supplementary Tables 1 and 2), a moderate yield of 3a was obtained in the absence of an exogenous ligand (entry 1, Table 1).
Acetaldehyde azine (AcAz) underwent 'crisscross' addition with two equivalents of phenyl isocyanate to form a one-to-two adduct in a moderate yield (63.0%).
The electrolyses experiments were carried out in an undivided cell under mild conditions without any toxic solvents, catalysts and supporting electrolytes, followed by addition of an alkylating agent, affording the α-hydroxycarboxylic acid methyl ester in a moderate yield (62%).
In the case of cyclohexene oxide, a moderate yield of 56 % with 63 % selectivity was obtained.
The main advantage of this synthesis is the higher yield of ligand precursors and a moderate yield of complex 64.
After the modest run scoring of the previous three Test seasons, Morris warmed up in 10 lead-in matches that yielded a moderate return of 347 runs at 34.70.
While aluminum amides, alkoxides, and aromatic organometallics were proven ineffective (entries 1 3), Me3Al in toluene produced the desired product 3 a in moderate yield (entry 4).
To our surprise, the addition of a Brønsted acid, such as HOAc, generated an approximately 1 1 mixture of 4 a and 5 a in moderate yields (Table 1, entry 9) and the use of p-toluenesulfonic acid (p-TSA) even did not afford any borylation products (Table 1, entry 10).
Every step of the reaction sequence proceeded smoothly and efficiently to give a good or moderate yield of the product (see the experimental section for the synthetic details).
These ynhydrazides were tested with the range of cyclization conditions discussed above; however, success was met only with reductive cyclization to give dienes 35 a– c in moderate yields (Scheme 9), with the stereochemistry assigned by H NMR nOe experiments.
