M
Mary J. Gresser
Researcher at University of Wollongong
Publications - 5
Citations - 1467
Mary J. Gresser is an academic researcher from University of Wollongong. The author has contributed to research in topics: Stereocenter & Enantioselective synthesis. The author has an hindex of 5, co-authored 5 publications receiving 1195 citations.
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Journal ArticleDOI
Atroposelective Synthesis of Axially Chiral Biaryl Compounds
Gerhard Bringmann,Anne J. Price Mortimer,Paul A. Keller,Mary J. Gresser,James Garner,Matthias Breuning +5 more
TL;DR: This Review classifies strategies in the asymmetric synthesis of axially chiral biaryl compounds according to their underlying concepts and critically evaluates their scope and limitations with reference to selected model reactions and applications.
Journal ArticleDOI
Atropselektive Synthese axial‐chiraler Biaryle
Gerhard Bringmann,Anne J. Price Mortimer,Paul A. Keller,Mary J. Gresser,James Garner,Matthias Breuning +5 more
TL;DR: In this paper, the Voraussetzungen fur das Auftreten von Axialchiralitat diskutiert werden anhand ausgewahlter Beispiele kritisch beurteilt.
Journal ArticleDOI
Atroposelective Synthesis of Axially Chiral Biaryl Compounds
Gerhard Bringmann,Anne J. Price Mortimer,Paul A. Keller,Mary J. Gresser,James Garner,Matthias Breuning +5 more
TL;DR: A review of axially chirality in biaryl compounds can be found in this paper, where the asymmetric information is introduced into a preformed, but achiral-that is, symmetric or configurationally labile-biaryl compound.
Journal ArticleDOI
The attempted stereoselective synthesis of chiral 2,2 '-biindoline
TL;DR: The first stereoselective synthesis of 2,2′-biindoline using a metathesis-Sharpless asymmetric dihydroxylation strategy was reported in this article.
Journal ArticleDOI
A new strategy for the stereoselective synthesis of 2,2′-bipyrrolidines
TL;DR: In this article, a new strategy for the stereoselective synthesis of the 2,2′-bipyrrolidine scaffold is presented using a metathesis reaction followed by asymmetric dihydroxylation for the introduction of the stereogenic elements.