Your English writing platform
Discover LudwigExact(2)
In short, these theoretical considerations lead to a partition of stimulus-bound eye movements into pursuit initiation, smooth pursuit and anticipatory pursuit, where each mode of oculomotor control calls on formal additions to the underlying generative model.
In short, these theoretical considerations lead to a partition of stimulus-bound eye movements into pursuit initiation, smooth pursuit and anticipatory pursuit, where each mode of oculomotor control calls on formal additions to the underlying generative model; however, they all use exactly the same scheme and basic principles.
Similar(58)
Hydroacylation, the formal addition of an aldehyde CH bond across an unsaturated functional group, is an ideal approach to carbonyl functionalities commonly found in bioactive molecules.
Structural analysis shows that these complexes are reduced by the formal addition of one hydride ion to each imino group, resulting in a deprotonated bis amido)pyridyl-thiolate ligand.
An upper-case letter indicates formal addition or substitution of a structural part.
This indicated formal addition of a CH2O unit to 4 epi.
This review summarizes recent methodologies for the simultaneous formation of C CF3 and C C or C heteroatom bonds by formal addition reactions to alkenes.
This reaction can be interpreted as the formal addition of a phosphide and a carbonyl across the Si=Si double bond.
This was consistent with a molecular formula of C35H40N4O9, as found in the HO-NCC 6 epi, suggesting the formal addition of an oxygen atom to 4 epi.
Nowadays, as happens for the addition of O-nucleophiles to alkynes, gold(I -catalyzed hydroamI -catalyzedlkynes is not limited to thydroaminationf imine of enalkynesroducts by formal addisionotf N–H reagents onto triplimiteds.
We have specially focused on methods involving the simultaneous formation of C CF3 and C C or C heteroatom bonds by formal addition reactions across π-systems, as such difunctionalization processes hold valuable synthetic potential.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com