Sentence examples for broad substrate scope of from inspiring English sources

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The binary catalyst system also showed broad substrate scope of epoxide.

The broad substrate scope of Ct-MAL has been exploited for the stereoselective synthesis of various N-, 3-, and N,3- di substituted aspartic acids (Akhtar et al. 1987; BottiN,3- di substitutedzaspartic. 1997).

Similar(58)

HOX [EC 1.1.3.5] from Chondrus crispus is an enzyme with a fairly broad substrate scope for the oxidation of sugars at C1. Hexose oxidase accepted d-xylose, d-arabinose and d-glucose containing di-sugars, like d-lactose and d-cellobiose (Table  7, entries 4, 5, 10 and 18) (Poulsen and Hostrup 1998; Savary et al. 2001; Rand et al. 2006).

The results disclose a broad substrate scope for the produced set of 22 BVMOs.

Notwithstanding the aforementioned examples, we set out to develop a new, user-friendly method for the dehydrogenation of hydrazones that offers a broad substrate scope and a simple purification of the diazo compound.

3 Despite this limitation, the advantages of this chelation-controlled process, such as mild reaction conditions, control of enantio- and regioselectivity, 4, 5 and broad substrate scope, have resulted in widespread applications of this approach.

Notably, Pd/ L124-catalyzed biaryl formation exhibited a relatively broad substrate scope, enabling the atroposelective cross-coupling of 1-bromonaphthalene or 1-bromo-2-methylnaphthalene with a variety of arylboronic acids.

To further improve and extend the scope of DKR reactions, more efficient and more enantioselective enzymes with broad substrate scope are required.

Synthesis of a variety of well-shaped chiral ligands as well as design of catalysts based on mechanistic understanding enable the creation of the reactive and selective catalysts with a broad substrate scope.

These single-electron oxidation reactions exhibit broad substrate scope, operational simplicity, and low catalyst cost under mild conditions without prefunctionalization of the substrate and without direct addition to an arylmetalate; however, a number of mechanistic questions, perhaps related to phase transfer considerations, remain unanswered.

Characterization of the purified enzyme revealed that it has a broad substrate scope and oxidized different compounds including substituted and unsubstituted alicyclic, bicyclic-, aliphatic-ketones, ketones with an aromatic moiety, and sulfides.

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