Tandem SN2-Michael addition to vinylogous carbonates for the stereoselective construction of 2,3,3,5-tetrasubstituted tetrahydrofurans-Reference-Cited by-同舟云学术

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Tandem SN2-Michael addition to vinylogous carbonates for the stereoselective construction of 2,3,3,5-tetrasubstituted tetrahydrofurans

Published:2010-11 Issue:47 Volume:51 Page:6093-6097
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Gharpure Santosh J.,Reddy S. Raja Bhushan

Funder

Council of Scientific and Industrial Research, India

Department of Science and Technology, Ministry of Science and Technology, India

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference48 articles.

1. Synthetic routes to tetrahydrofuran, tetrahydropyran, and spiroketal units of polyether antibiotics and a survey of spiroketals of other natural products

2. Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediates

3. Synthetic routes to 2,5-disubstituted tetrahydrofurans

4. Stereoselective Synthesis of Oligo-Tetrahydrofurans

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1. Ni-Catalyzed Formal Cross-Electrophile Coupling of Alcohols with Aryl Halides;ACS Catalysis;2021-11-05

2. Cascade Radical Cyclization to Vinylogous Carbonates/Carbamates for the Synthesis of Oxa- and Aza-Angular Triquinanes: Diastereoselectivity Depends on the Ring Size of Radical Precursor;Synthesis;2018-07-11

3. Lewis Acid Mediated “endo-dig” Hydroalkoxylation–Reduction on Internal Alkynols for the Stereoselective Synthesis of Cyclic Ethers and 1,4-Oxazepanes;Organic Letters;2017-11-22

4. Base-Free and Catalyst-Free Synthesis of Functionalized Dihydrobenzoxazoles via Vinylogous Carbonate to Carbamate Rearrangement;Organic Letters;2017-10-02

5. Recent advances in the synthesis of tetrahydrofurans and applications in total synthesis;Tetrahedron;2016-08

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