Search Results - "Struble, Justin"

Highly Enantioselective Azadiene Diels−Alder Reactions Catalyzed by Chiral N-Heterocyclic Carbenes by He, Ming, Struble, Justin R, Bode, Jeffrey W

“…Highly enantioselective, N-heterocyclic carbene (NHC)-catalyzed aza-Diels−Alder reactions are described. A novel chiral triazolium salt based on the…”
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Synthesis of an N-Mesityl Substituted Chiral Imidazolium Salt for NHC-Catalyzed Reactions by Struble, Justin R, Kaeobamrung, Juthanat, Bode, Jeffrey W

“…A new synthetic approach to chiral imidazolium salts makes possible the first synthesis of an N-mesityl substituted, aminoindanol-derived N-heterocyclic…”
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Formal synthesis of salinosporamide A via NHC-catalyzed intramolecular lactonization by Struble, Justin R., Bode, Jeffrey W.

“…An N-heterocyclic carbene (NHC) catalyzed intramolecular lactonization to prepare densely functionalized bicyclic γ-lactam-γ-lactone adducts from enals is…”
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( Z)-(2-Bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis by Woerly, Eric M., Struble, Justin R., Palyam, Nagarjuna, O’Hara, Sean P., Burke, Martin D.

“…Iterative cross-coupling represents a potentially general approach for the simple, efficient, and flexible construction of a wide range of functional small…”
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Ethynyl MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis by Struble, Justin R., Lee, Suk Joong, Burke, Martin D.

“…Ethynyl N-methyliminodiacetic acid (MIDA) boronate is a very useful building block for small molecule synthesis. This compound can serve as both a bifunctional…”
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A modular synthesis of chiral aminoindanol-derived imidazolium salts by Struble, Justin R., Bode, Jeffrey W.

“…A modular synthesis of N-substituted chiral imidazolium salts derived from (1 R,2 S)-(+)-1-amino-2-indanol is described. A wide range of amines are amenable to…”
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Development of a Practical Process for the Large-Scale Preparation of the Chiral Pyridyl-Backbone for the Crabtree/Pfaltz-Type Iridium Complex Used in the Industrial Production of the Novel Fungicide Inpyrfluxam by Jones, Michelle, Harris, Dave, Struble, Justin, Hayes, Michael, Koeller, Kevin, Chepiga Özgün, Kathryn, Schirmer, Heiko, Heinrich, Jens, Baechle, Florian, Goudedranche, Sebastien, Schotes, Christoph

“…Herein, we report the development activities leading to an efficient process for the large-scale production of the key intermediate to a crabtree/pfaltz-type…”
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A new process to prepare 3,6-dichloro-2-hydroxybenzoic acid, the penultimate intermediate in the synthesis of herbicide dicamba by Walker, Daniel P., Harris, G. Davis, Carroll, Jeffery N., Boehm, Terri L., McReynolds, Matthew D., Struble, Justin R., van Herpt, Jochem, van Zwieten, Don, Koeller, Kevin J., Bore, Mangesh

“…[Display omitted] •3,6-Dichloro-2-hydroxybenzoic acid (3,6-DCSA) can be prepared in four steps from salicylic acid.•3,6-DCSA can be prepared without the need…”
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Ethynyl MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis: Tetrahedron Young Investigator Award 2010 Recent Developments in Synthetic Methods and Total Synthesis Brian Stoltz by STRUBLE, Justin R, SUK JOONG LEE, BURKE, Martin D

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(Z)-(2-Bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis: Tetrahedron Young Investigator award 2011. Useful Synthetic Methods: Innovative Developments and Applications. F. Dean Toste by WOERLY, Eric M, STRUBLE, Justin R, PALYAM, Nagarjuna, O'HARA, Sean P, BURKE, Martin D

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N -heterocyclic carbenes: From design to synthesis and their application as nucleophilic catalysts by Struble, Justin R

“…Our group has pioneered novel internal redox process of aldehydes possessing an internal α-reducible functionality mediated by N-heterocyclic carbenes (NHCs)…”
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N-heterocyclic carbenes: From design to synthesis and their application as nucleophilic catalysts by Struble, Justin R

“…Our group has pioneered novel internal redox process of aldehydes possessing an internal alpha-reducible functionality mediated by N-heterocyclic carbenes…”
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