SnCl<sub>2</sub>-catalyzed multicomponent coupling: synthesis of 1,3-oxazolidine derivatives using paraformaldehyde as a C1 feedstock-Reference-Cited by-同舟云学术

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SnCl₂-catalyzed multicomponent coupling: synthesis of 1,3-oxazolidine derivatives using paraformaldehyde as a C1 feedstock

Published:2024 Issue:28 Volume:22 Page:5768-5775
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Nayak Mukesh Kumar¹,Chakraborty Swati¹,Mohanty Anuradha¹,Roy Sujit¹^ORCID

Affiliation:

1. Organometallics & Catalysis Laboratory, School of Basic Sciences, Indian Institute of Technology Bhubaneswar, Arugul, Jatani, Khurda 752050, Odisha, India

Abstract

Base- and additive-free synthesis of 1,3-oxazolidine derivatives has been achieved in a straightforward manner with low catalyst loading using paraformaldehyde as a C1 platform chemical.

Funder

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00791C

Reference54 articles.

1. Recent advances in the multicomponent synthesis of heterocycles using tetronic acid

2. Bioactive 2-pyridone-containing heterocycle syntheses using multicomponent reactions

3. Recent advances in multi-component reactions and their mechanistic insights: a triennium review

4. J.Zhu , Q.Wang and M. X.Wang , Multicomponent Reactions in Organic Synthesis , Wiley Blackwell , 2015

5. Recent advances in organic synthesis with CO2 as C1 synthon

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