An Environmentally Benign Synthesis of cis-2,6-Disubstituted Tetrahydropyrans via Indium-Mediated Tandem Allylation/Prins Cyclization Reaction
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, California State UniversityNorthridge, Northridge, California 91330 thomas.minehan@csun.edu
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo7016857
Reference19 articles.
1. An expedient synthesis of (±)-centrolobine
2. A Novel Stereoselective Cyclization to Functionalized Dihydropyrans
3. SILYLATION OF 2-METHYL-2-PROPEN-1-OL DIANION: 2-(HYDROXYMETHYL)ALLYLTRIMETHYLSILANE
4. Synthesis of Oxa-Bridged 7- and 8-Membered Rings via Indium-Mediated Annulation of 1,4- and 1,5-Dicarbonyl Compounds with 3-Iodo-2-[(trimethylsilyl)methyl]propene
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1. Advances in the Study of the Prins Reaction and the Prins Cyclization Reaction;Journal of Organic Chemistry Research;2024
2. Prins cyclization-mediated stereoselective synthesis of tetrahydropyrans and dihydropyrans: an inspection of twenty years;Beilstein Journal of Organic Chemistry;2021-04-29
3. Gallium and Indium Complexes in Organic Synthesis;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2021
4. Enantioselective Synthesis of cis ‐2, 6‐Disubstituted ‐4‐methylene Tetrahydropyrans via Chromium Catalysis †;Chinese Journal of Chemistry;2020-10-14
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