New methodology for the synthesis of tetrahydrofuro[3,2-b]furan-2(3H)-one derivatives, synthons of natural products with biological interest-Reference-Cited by-同舟云学术

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New methodology for the synthesis of tetrahydrofuro[3,2-b]furan-2(3H)-one derivatives, synthons of natural products with biological interest

Published:2016-10 Issue:43 Volume:72 Page:6794-6806
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Montaña Ángel M.,Barcia Joan A.,Grima Pedro M.,Kociok-Köhn Gabriele

Funder

Spanish Ministry of Economics and Competitiveness (MINECO)

University of Barcelona

Generalitat de Catalunya

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference132 articles.

1. Synthesis and antitumor activity of goniofufurone analogues

2. Wittig reaction with partially protected sugar lactol derivatives. Preparation of highly cytotoxic goniofufurone analogues

3. Sulfur-Mediated Synthesis of Substituted Tetrahydrofurans: Application to the Synthesis of Goniofufurone

4. Accessing tetrahydrofuran-based natural products by microbial Baeyer–Villiger biooxidation

5. Total synthesis of antitumor agents, (+)-goniopypyrone and (+)-7-epi-goniofufurone

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1. α‐Halocarbonyls as a Valuable Functionalized Tertiary Alkyl Source;ChemistryOpen;2024-07-11

2. Design and synthesis of new antitumor agents with the 1,7-epoxycyclononane framework. Study of their anticancer action mechanism by a model compound;Bioorganic & Medicinal Chemistry;2018-07

3. Synthesis of the 10-oxabicyclo[5.2.1]decane framework present in bioactive natural products;Organic & Biomolecular Chemistry;2018

4. A H2O2/HBr system – several directions but one choice: oxidation–bromination of secondary alcohols into mono- or dibromo ketones;RSC Advances;2018

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