Search Results - "Janey, Jacob"
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1
Bayesian reaction optimization as a tool for chemical synthesis
Published in Nature (London) (04-02-2021)“…Reaction optimization is fundamental to synthetic chemistry, from optimizing the yield of industrial processes to selecting conditions for the preparation of…”
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2
Recent Advances in Catalytic, Enantioselective α Aminations and α Oxygenations of Carbonyl Compounds
Published in Angewandte Chemie International Edition (11-07-2005)“…The direct introduction of either a nitrogen or oxygen atom adjacent to a carbonyl group in a catalytic, enantioselective manner using both chiral Lewis acid…”
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3
Biocatalytic Asymmetric Synthesis of Chiral Amines from Ketones Applied to Sitagliptin Manufacture
Published in Science (American Association for the Advancement of Science) (16-07-2010)“…Pharmaceutical synthesis can benefit greatly from the selectivity gains associated with enzymatic catalysis. Here, we report an efficient biocatalytic process…”
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4
Development of a Platform for Near-Infrared Photoredox Catalysis
Published in ACS central science (25-11-2020)“…Over the past decade, chemists have embraced visible-light photoredox catalysis due to its remarkable ability to activate small molecules. Broadly, these…”
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5
Scalable Asymmetric Synthesis of MK-8998, a T‑Type Calcium Channel Antagonist
Published in Journal of organic chemistry (18-02-2022)“…Two scalable and efficient synthetic routes for the synthesis of a T-type calcium channel antagonist MK-8998 were developed from a simple pyridine building…”
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6
Direct Lewis Acid Catalyzed Conversion of Enantioenriched N‑Acyloxazolidinones to Chiral Esters, Amides, and Acids
Published in Journal of organic chemistry (07-12-2018)“…The identification of Yb(OTf)3 through a multivariable high-throughput experimentation strategy has enabled a unified protocol for the direct conversion of…”
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7
Synthesis of Vibegron Enabled by a Ketoreductase Rationally Designed for High pH Dynamic Kinetic Reduction
Published in Angewandte Chemie International Edition (04-06-2018)“…Described here is an efficient stereoselective synthesis of vibegron enabled by an enzymatic dynamic kinetic reduction that proceeds in a high‐pH environment…”
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8
Enantioselective Synthesis of a γ‑Secretase Modulator via Vinylogous Dynamic Kinetic Resolution
Published in Journal of organic chemistry (21-09-2018)“…Two efficient asymmetric routes to γ-secretase modulator BMS-932481, under investigation for Alzheimer’s disease, have been developed. The key step for the…”
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9
Proline-Catalyzed, Asymmetric Mannich Reactions in the Synthesis of a DPP-IV Inhibitor
Published in Journal of organic chemistry (06-01-2006)“…A highly stereoselective l-proline-catalyzed, asymmetric direct Mannich reaction between a glyoxalate-derived imine and phenyl acetaldehyde was employed for…”
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10
A biocatalytic/reductive etherification approach to substituted piperidinyl ethers
Published in Tetrahedron (29-07-2014)“…A synthetically useful protocol has been developed for the preparation of highly functionalized piperidinyl ethers. Biocatalytic reduction of cyclhexanones 7,…”
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11
Practical Synthesis of A Macrocyclic HCV Protease Inhibitor: A High-Yielding Macrolactam Formation
Published in Organic process research & development (21-03-2014)“…A practical synthesis of a macrocyclic HCV protease inhibitor, MK-1220, is described. The key features are a new synthesis of the trisubstituted isoquinoline,…”
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12
A Practical Synthesis of 5-Lipoxygenase Inhibitor MK-0633
Published in Journal of organic chemistry (18-06-2010)“…Practical, chromatography-free syntheses of 5-lipoxygenase inhibitor MK-0633 p-toluenesulfonate (1) are described. The first route used an asymmetric zincate…”
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13
C 2-Symmetric Cu(II) Complexes as Chiral Lewis Acids. Catalytic, Enantioselective Cycloadditions of Silyl Ketenes
Published in Organic letters (28-06-2001)“…C 2-Symmetric bis(oxazoline)−Cu(II) complexes (4a−g) catalyze the enantioselective [2 + 2] cycloaddition between (silyl)ketenes and chelating carbonyl…”
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14
Synthesis of Vibegron Enabled by a Ketoreductase Rationally Designed for High pH Dynamic Kinetic Reduction
Published in Angewandte Chemie (04-06-2018)“…Described here is an efficient stereoselective synthesis of vibegron enabled by an enzymatic dynamic kinetic reduction that proceeds in a high‐pH environment…”
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15
Raney-Co Mediated Reductive Cyclization of an α,β-Unsaturated Nitrile
Published in Journal of organic chemistry (18-04-2008)“…An expedient, five step synthesis of caprolactam 1 is reported starting from natural L-homoserine. The key step is a chemoselective reductive cyclization of…”
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16
Racemic and Asymmetric Diels−Alder Reactions of 1-(2-Oxazolidinon-3-yl)-3-siloxy-1,3-butadienes
Published in Journal of organic chemistry (29-12-2000)“…Achiral and chiral 1-(2-oxazolidinon-3-yl)-3-siloxy-1,3-butadienes were prepared from readily available starting materials. Although more stable than the…”
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17
1-Amino-3-siloxy-1,3-butadienes: Highly Reactive Dienes for the Diels−Alder Reaction
Published in Journal of organic chemistry (30-04-1999)“…1-Amino-3-siloxy-1,3-butadienes represent a novel class of heteroatom-containing dienes with several useful properties. These dienes can be prepared…”
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18
Solubility Behaviors and Correlations of Common Organic Solvents
Published in Organic process research & development (20-11-2020)“…Through a statistical analysis of empirical solubility data collected from over 1000 solutes, the solubility behaviors of 53 common solvents are characterized…”
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19
Solubility Behaviors and Correlations of Common Solvent–Antisolvent Systems
Published in Organic process research & development (20-11-2020)“…This report is a follow-up to our two prior publications that analyzed solubility behaviors and correlations of common solvents. The statistical results…”
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20
Synergistic Solvation Effects: Enhanced Compound Solubility Using Binary Solvent Mixtures
Published in Organic process research & development (19-07-2019)“…We explain the concept of solubility synergistic solvation (also known as parabolic solubility), wherein a binary solvent mixture exhibits a higher solubility…”
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