Enantioselective Construction of Cis-2,6-Disubstituted Dihydropyrans: Total Synthesis of (−)-Centrolobine-Reference-Cited by-同舟云学术

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Enantioselective Construction of Cis-2,6-Disubstituted Dihydropyrans: Total Synthesis of (−)-Centrolobine

Published:2010-01-29 Issue:5 Volume:75 Page:1740-1743
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chaładaj Wojciech¹,Kowalczyk Rafał²,Jurczak Janusz¹³

Affiliation:

1. Institute of Organic Chemistry, Polish Academy of Sciences, 01-224 Warsaw, Poland

2. Department of Organic Chemistry, Faculty of Chemistry, Wrocław University of Technology, 50-370 Wrocław, Poland

3. Department of Chemistry, Warsaw University, 02-093 Warsaw, Poland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo902167r

Reference58 articles.

1. Marine natural products: synthetic aspects

2. Evolution of the Petasis−Ferrier Union/Rearrangement Tactic: Construction of Architecturally Complex Natural Products Possessing the Ubiquitous cis-2,6-Substituted Tetrahydropyran Structural Element

3. Strategies for the Formation of Tetrahydropyran Rings in the Synthesis of Natural Products

4. First Enantioselective Total Synthesis of (−)-Centrolobine

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1. Facile acid-mediated one-pot synthesis of dihydropyran and furan derivatives in aqueous media;Tetrahedron Letters;2024-10

2. An Efficient Stereoselective Synthesis of cis-2,6-Disubstituted Tetrahydropyrans via Gold-Catalyzed Meyer–Schuster Rearrangement/Hydration/oxa-Michael Addition Sequence;Catalysts;2024-03-29

3. Pyrans and Their Benzo Derivatives: Structure and Reactivity;Comprehensive Heterocyclic Chemistry IV;2022

4. Total Syntheses of Centrolobines: A Two‐Decade Journey;ChemistrySelect;2021-12

5. Catalytic δ-hydroxyalkynone rearrangement in the stereoselective total synthesis of centrolobine, engelheptanoxides A and C and analogues;Tetrahedron;2021-09

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