Results 101 to 110 of about 149,811 (326)
A unique method for highly enantioselective synthesis of N–C axially chiral compounds [PDF]
Osamu Kitagawa
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This study explores the reasons behind the variations in the enantioselectivity of the sulfoxidation of methyl phenyl sulfide by marine-derived vanadium-dependent haloperoxidases (VHPOs). Twelve new VHPOs of marine organisms were overexpressed, purified,
Yun-Han Zhang +4 more
doaj +1 more source
A novel aldo-keto reductase Tm1743 characterized from Thermotoga maritima was explored as an effective biocatalyst in chiral alcohol production. Natural Tm1743 catalyzes asymmetric reduction of ethyl 2-oxo-4-phenylbutyrate (EOPB) at high efficiency, but ...
Zhiguo Wang +7 more
doaj +1 more source
Intermolecular Enantioselective Nickel‐Catalyzed Arylation of Un‐Activated C(sp3)─H Bond
Ni: a new solution for asymmetric C(sp3)─H activation. The stereoselective synthesis of all‐carbon quaternary stereogenic centres is achieved via enantioselective C(sp3)─H arylation using a Ni‐BINOL‐derived catalyst. Rational catalytic cycle design uncovers a new reaction pathway that can efficiently induce chiral information during the stereoselective
Erwan Brunard +4 more
wiley +1 more source
C2-Symmetric Dinickel Catalysts for Enantioselective [4 + 1]-Cycloadditions
Michael J. Behlen, Christopher Uyeda
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Photochemical Deracemization of Chromanes and its Application to the Synthesis of Enantiopure Bioactive Compounds. [PDF]
Various substituted chromane‐2‐carboxamides were successfully deracemized by employing a chiral benzophenone (BP, 10 mol%) as photocatalyst and an achiral thiol as additive (20 mol%). The method was applied to the concise enantioselective synthesis of five active pharmaceutical ingredients.
Ghosh B +5 more
europepmc +3 more sources
Essential oil composition and enantioselective profile of Juniperus communis var. depressa (Cupressaceae) from Utah [PDF]
Ariel Poulson +5 more
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Synthesis of α‐Pentafluorosulfanylated‐β2,3‐Amino Esters
De novo α‐SF5‐β2,3‐amino esters are now accessible through a straightforward aza‐Michael reaction using a series of newly developed (E)‐α‐SF5‐α,β‐unsaturated esters. Two new, highly functionalized, contiguous tertiary stereocenters are formed with diastereodivergence governed by the choice of solvent and/or base.
Thi Mo Nguyen +5 more
wiley +1 more source

