Results 91 to 100 of about 415,153 (176)
A convenient and efficient method for the synthesis of (–)-bestatin, epibestatin, phebestin, and (3S,4R)-4-amino-3-hydroxy-5-phenylpentanoic acid is reported. The key step is a proline-catalyzed α-hydroxylation of an aldehyde derived from d-phenylalanine,
Vipin Kumar Jain
doaj +1 more source
Epoxides: Small Rings to Play with under Asymmetric Organocatalysis. [PDF]
Meninno S, Lattanzi A.
europepmc +1 more source
Enantioselective organocatalysis has become a field of central importance within asymmetric chemical synthesis and appears to be efficient approach toward the construction of complex chiral molecules from simple achiral materials in one-pot ...
Chittaranjan Bhanja +3 more
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Asymmetric Organocatalysis in the Remote (3 + 2)-Cycloaddition to 4-(Alk-1-en-1-yl)-3-cyanocoumarins. [PDF]
Łukasik B +3 more
europepmc +1 more source
(Thio)urea-mediated synthesis of functionalized six-membered rings with multiple chiral centers
Organocatalysis, now running its second decade of life, is being considered one of the main tools a synthetic chemist has to perform asymmetric catalysis. In this review the synthesis of six-membered rings, that contain multiple chiral centers, either by
Giorgos Koutoulogenis +2 more
doaj +1 more source
Green Chemistry Meets Asymmetric Organocatalysis: A Critical Overview on Catalysts Synthesis. [PDF]
Antenucci A, Dughera S, Renzi P.
europepmc +1 more source
New Concepts for Organocatalysis
Organocatalysis, catalysis with low-molecular weight catalysts in which a metal is not part of the catalytic principle or the reaction substrate, can be as efficient and selective as metal- or biocatalysis.
List, B., B. List, Pan, S., S. C. Pan
core +1 more source
Chiral proline-substituted porous organic cages in asymmetric organocatalysis. [PDF]
Xu N, Su K, El-Sayed EM, Ju Z, Yuan D.
europepmc +1 more source
Synthesis of the Southern Tripeptide (C1–N12) of Sanglifehrins Using Asymmetric Organocatalysis
The tripeptide southern region of the novel cyclophilin binding natural product macrolides, namely sanglifehrins, is synthesized involving asymmetric organocatalysis as chirality-inducing step.
Laghuvarapu Radhika (626159) +1 more
core +1 more source
Asymmetric Counteranion-Directed Lewis Acid Organocatalysis.
This work describes studies on asymmetric counteranion-directed Lewis acid organocatalysis. In the first part, the development of a catalytic asymmetric Hosomi–Sakurai reaction using BINOL-derived disulfonimides is described. Good to excellent yields and
van Gemmeren, M.
core

