J
Jack L.-Y. Chen
Researcher at Auckland University of Technology
Publications - 34
Citations - 811
Jack L.-Y. Chen is an academic researcher from Auckland University of Technology. The author has contributed to research in topics: Chemistry & Total synthesis. The author has an hindex of 14, co-authored 30 publications receiving 666 citations. Previous affiliations of Jack L.-Y. Chen include University of Auckland & University of Padua.
Papers
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Journal ArticleDOI
An Amphiphilic (salen)Co Complex – Utilizing Hydrophobic Interactions to Enhance the Efficiency of a Cooperative Catalyst
Pablo Solís-Muñana,Pablo Solís-Muñana,Joanne Salam,Joanne Salam,Chloe Z.-J. Ren,Chloe Z.-J. Ren,Bronte Carr,Andrew E. Whitten,Gregory G. Warr,Jack L.-Y. Chen,Jack L.-Y. Chen,Jack L.-Y. Chen +11 more
Journal ArticleDOI
Simultaneous extraction, derivatisation and analysis of varietal thiols and their non-volatile precursors from beer
Rebecca E. Jelley,Hayden Jones-Moore,Angela Guan,Chloe Z.-J. Ren,Jack L.-Y. Chen,Loris Tonidandel,Roberto Larcher,Bruno Fedrizzi +7 more
TL;DR: In this paper , a QuEChERS protocol was developed to extract varietal thiols and precursors from beer, and Ebselen derivatisation enabled non-volatile varietal Thiols analysis using LC-MS/MS.
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Light-Switchable Membrane Permeability in Giant Unilamellar Vesicles
Paola Albanese,Simone Cataldini,Chloe Z.-J. Ren,Nadia Valletti,Jlenia Brunetti,Jack L.-Y. Chen,Federico Rossi +6 more
TL;DR: In this paper , a photoisomerized giant unilamellar vesicles (GUVs) were synthesized by blending the natural phospholipid 1-palmitoyl-2-oleoylsn-glycero-3-phosphocholine (POPC) with a photoswitchable amphiphile.
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Enantiospecific, Regioselective Cross‐Coupling Reactions of Secondary Allylic Boronic Esters.
Laetitia Chausset‐Boissarie,Kazem Ghozati,Emily LaBine,Jack L.-Y. Chen,Varinder K. Aggarwal,Cathleen M. Crudden,Cathleen M. Crudden +6 more
TL;DR: The Suzuki-Miyaura cross-coupling of enantioenriched secondary allylic boronic esters occurs with high γ-regioselectivity and high retention of chirality, proceeding via γ -selective transmetalation and subsequent reductive elimination.
Journal ArticleDOI
Tandem Allylboration-Prins Reaction for the Rapid Construction of Substituted Tetrahydropyrans: Application to the Total Synthesis of (-)-Clavosolide A.
TL;DR: In this article, a three-component allylboration-Prins reaction sequence was used to synthesize tetrahydropyrans with high stereocontrol for macrolide (−)-clavosolide A. The synthesis also features an early stage glycosidation reaction to introduce the xylose moiety.