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C&EN5d
One-Pot Modified Madelung Synthesis of 3-Tosyl- and 3-Cyano-1,2-disubstituted Indoles
Creative Commons (CC): This is a Creative Commons license. Attribution (BY): Credit must be given to the creator. Non-Commercial (NC): Only non-commercial uses of the work are permitted. Article Views ...
C&EN6d
Catalytic Synthesis of Enantiopure Chiral Alcohols via Addition of Grignard Reagents to Carbonyl Compounds
‡ Division of Chemistry and Environmental Science, Faculty of Science and Engineering, Manchester Metropolitan University, John Dalton Building, Oxford Road, M1 5GD Manchester, U.K. Article Views are ...
C&EN6d
Discovery of Indoles as Potent and Selective Inhibitors of the Deacetylase SIRT1
Elixir Pharmaceuticals, One Kendall Square, Cambridge, Massachusetts 02139, EvotecOAI, 151 Milton Park, Abingdon OX14 4SD, U.K., and Advanced Synthesis Group ... Preparation of enantiomerically pure ...
Science Daily6d
Two plant species invent the same chemically complex and medically interesting substance
The biosynthesis of the great variety of natural plant products has not yet been elucidated for many medically interesting substances. In a new study, an international team of researchers was able to ...
C&EN6d
Enantioselective Alkenylation of Aldimines Catalyzed by a Rhodium–Diene Complex
† College of Life Sciences, Northwest University, Xi’an, Shaanxi 710069, P. R. China ‡ CAS Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese ...
C&EN7d
Indole Diterpenoid Synthetic Studies. Construction of the Heptacyclic Core of (−)-Nodulisporic Acid D
The modular synthetic strategy comprises an expedient, stereocontrolled synthesis of a tricyclic western hemisphere, in conjunction with union of an eastern hemisphere, exploiting the 2-substituted ...
C&EN7d
Stereoselective Synthesis of a MCHr1 Antagonist
Chemistry Process Research and Development, Amgen Inc., Thousand Oaks, California 19320, Medicinal Chemistry, Amgen SF, South San Francisco, California 94080, Process ...
C&EN10d
Synthesis of Azacarbolines via PhIO
Department of Biomolecular Sciences, Section of Chemistry and Pharmaceutical Technologies, University of Urbino “Carlo Bo”, Via I Maggetti 24, 61029 Urbino, Italy ...
C&EN10d
Novel Indole-Based Peroxisome Proliferator-Activated Receptor Agonists: Design, SAR, Structural Biology, and Biological Activities
Division of Biotechnology and Pharmaceutical Research, National Health Research Institutes, 35 Keyan Road, Zhunan Town, Miaoli County 350, Taiwan, Republic of China, and Department of Chemistry and ...
C&EN11d
Palladium Nanoparticles Confined in the Cages of MIL-101: An Efficient Catalyst for the One-Pot Indole Synthesis in Water
† The Education Ministry Key Lab of Resource Chemistry and Shanghai Key Laboratory of Rare Earth Functional Materials, Shanghai Normal University, Shanghai 200234, P.R. China ‡ Department of Chemistry ...
C&EN13d
Synthesis of C2-Carbonyl Indoles via Visible Light-Induced Oxidative Cleavage of an Aminomethylene Group
Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Provincial Center for Research & Development of Natural Products, School of Pharmacy, Yunnan University, ...
C&EN13d
Structure−Property Relationships of Copolymers Obtained by Ring-Opening Polymerization of Glycolide and ε-Caprolactone. Part 1. Synthesis and Characterization
Centre of Polymer Chemistry, Polish Academy of Sciences, 34 Sklodowska Curie st. 41-808 Zabrze, Poland, and Centre de Recherche sur les Biopolymeres Artificiels, Faculte de Pharmacie, 15 avenue ...