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Recent Advances in Organic Synthetic Methods

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Organic Chemistry".

Deadline for manuscript submissions: closed (30 January 2020) | Viewed by 3485

Special Issue Editor


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Guest Editor
Department of Chemistry, Oklahoma State University, Stillwater, OK, USA
Interests: new synthetic methodology; heterocycles; antibacterial agents; anticancer agents; medicinal chemistry
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

The development of new synthetic methodology is essential to gain/improve access to natural and unnatural organic compounds. Recent advances in this area have led to the development of many new reagents and strategies for use in the synthesis of natural products, drugs, and structures of theoretical interest. For this Special Issue of Molecules, entitled "Recent Advances in Organic Synthetic Methods", I invite authors to submit manuscripts that focus on new reagents with the ability to efficiently access synthetically versatile functionality or new approaches to the preparation of functionalized core structures with potential for use in natural product or drug synthesis. Of particular interest are manuscripts which summarize existing strategies and the advantages of new methods over current procedures. Further information on the mechanisms (for new reactions) and scopes of new methods should also be included. Original research articles or reviews that discuss the development and use of new synthetic methods are also welcome.

Prof. Dr. Richard A. Bunce
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Molecules is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • organic synthetic method
  • new reagent
  • functional group introduction
  • annulation strategies
  • synthetic efficiency

Published Papers (1 paper)

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Research

9 pages, 1780 KiB  
Communication
Direct Dehydrative Glycosylation Catalyzed by Diphenylammonium Triflate
by Mei-Yuan Hsu, Sarah Lam, Chia-Hui Wu, Mei-Huei Lin, Su-Ching Lin and Cheng-Chung Wang
Molecules 2020, 25(5), 1103; https://0-doi-org.brum.beds.ac.uk/10.3390/molecules25051103 - 02 Mar 2020
Cited by 7 | Viewed by 3103
Abstract
Methods for direct dehydrative glycosylations of carbohydrate hemiacetals catalyzed by diphenylammonium triflate under microwave irradiation are described. Both armed and disarmed glycosyl-C1-hemiacetal donors were efficiently glycosylated in moderate to excellent yields without the need for any drying agents and stoichiometric additives. This method [...] Read more.
Methods for direct dehydrative glycosylations of carbohydrate hemiacetals catalyzed by diphenylammonium triflate under microwave irradiation are described. Both armed and disarmed glycosyl-C1-hemiacetal donors were efficiently glycosylated in moderate to excellent yields without the need for any drying agents and stoichiometric additives. This method has been successfully applied to a solid-phase glycosylation. Full article
(This article belongs to the Special Issue Recent Advances in Organic Synthetic Methods)
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