Synthesis of 1-arylidene-2,3-dihydro-1H-inden-2-ols through a tandem carbopalladation/Suzuki–Miyaura sequence
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Cyclic Carbopalladation. A Versatile Synthetic Methodology for the Construction of Cyclic Organic Compounds
2. A Domino Sequence Consisting of Insertion, Coupling, Isomerization, and Diels-Alder Steps Yields Highly Fluorescent Spirocycles
3. A Tandem Heck-Carbocyclization/Suzuki-Coupling Approach to the Stereoselective Syntheses of Asymmetric 3,3-(Diarylmethylene)indolinones
4. Stereoselective Synthesis of 3-Alkylideneoxindoles via Palladium-Catalyzed Domino Reactions
5. Tandem Heck–Suzuki–Miyaura reaction: Application to the synthesis of constrained analogues of combretastatin A-4
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1. Stereoselective Domino Heck‐Suzuki Reactions;European Journal of Organic Chemistry;2022-12-30
2. Intramolecular Anti ‐Carbolithiation of Alkynes: Stereo‐Directing Effect of Lithium‐Coordinating Substituents;European Journal of Organic Chemistry;2022-01-12
3. Palladium-catalysed stereoselective synthesis of 4-(diarylmethylidene)-3,4-dihydroisoquinolin-1(2H)-ones: expedient access to 4-substituted isoquinolin-1(2H)-ones and isoquinolines;Organic & Biomolecular Chemistry;2018
4. Development of a Pd-Catalyzed Dearomative 1,2-Diarylation of Indoles Using Aryl Boron Reagents;Springer Theses;2018
5. A Mild, Functional Group Tolerant Addition of Organozinc Nucleophiles to N-Activated Quinolines and Isoquinolines;The Journal of Organic Chemistry;2017-09-07
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