Micellar catalysis enabled synthesis of indolylbenzothiazoles and their functionalization via Mn(II)-catalyzed C2–H amination using pyridones-Reference-Cited by-同舟云学术

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Micellar catalysis enabled synthesis of indolylbenzothiazoles and their functionalization via Mn(II)-catalyzed C2–H amination using pyridones

Published:2020-06 Issue:25 Volume:61 Page:152017
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kumar Sanjeev,Parshuram Satpute Dinesh,Nikhil Vaidya Gargi,Nagpure Mithilesh,Kumar Lokhande Shyam,Meena Deepak,Kumar Dinesh

Funder

Science and Engineering Research Board, Department of Science and Technology (DST-SERB), Government of India

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference76 articles.

1. Green and Sustainable Solvents in Chemical Processes

2. Role of Biocatalysis in Sustainable Chemistry

3. Catalytic Conversion of Carbohydrates to Initial Platform Chemicals: Chemistry and Sustainability

4. Design of Sustainable Chemical ProductsThe Example of Ionic Liquids

5. More Sustainable Approaches for the Synthesis of N-Based Heterocycles

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1. An integrative sustainability assessment of the Tsuji–Trost reaction simulating allylic amination under non-conventional (vs. conventional) conditions;Green Chemistry;2024

2. Catalysis and inhibition of ester hydrolysis by encapsulation in micelles derived from designer surfactant TPGS-750-M;Tetrahedron;2023-03

3. TPGS‐750‐M;Encyclopedia of Reagents for Organic Synthesis;2022-02-26

4. Oxidation step in the preparation of benzocamalexin: The crystallographic evidence;Mendeleev Communications;2021-11

5. Manganese‐catalyzed amination reactions: An overview;Applied Organometallic Chemistry;2021-09-12

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