An Efficient Synthesis of Oxazolidines by Tandem Ring-Opening / Closing Reaction of Ts-Aziridine Using Formic Acid-Reference-Cited by-同舟云学术

An Efficient Synthesis of Oxazolidines by Tandem Ring-Opening / Closing Reaction of Ts-Aziridine Using Formic Acid

Published:2018-10-08 Issue:37 Volume:3 Page:10509-10514
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Chakraborty Ghosal Nirnita¹,De Aramita¹,Mahato Sachinta¹,Santra Sougata²,V. Zyryanov Grigory²³,Majee Adinath¹^ORCID

Affiliation:

1. Department of Chemistry; Visva-Bharati (A Central University), Santiniketan; 731235 India.

2. Department of Organic and Biomolecular Chemistry; Chemical Engineering Institute; Ural Federal University; 19 Mira Street 620002 Yekaterinburg Russian Federation.

3. I. Ya. Postovskiy Institute of Organic Synthesis; Ural Division of the Russian Academy of Sciences; 22 S. Kovalevskoy Street 620219 Yekaterinburg Russian Federation.

Funder

DST-RSF Major Research Project

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/slct.201802657/fullpdf

Reference43 articles.

1. Total Synthesis of (−)-Tetrazomine. Determination of the Stereochemistry of Tetrazomine and the Synthesis and Biological Activity of Tetrazomine Analogues

2. Synthesis of a netropsin conjugate of a water-soluble epi -quinocarcin analogue: the importance of stereochemistry at nitrogen

3. Synthesis and in vitro antibacterial activity of oxazolidine LBM-415 analogs as peptide deformylase inhibitors

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