ArticleAngewandte Chemie (International ed. in English)2013
Cascade approach to stereoselective polycyclic ether formation: epoxides as trapping agents in the transposition of allylic alcohols.
Article in Angewandte Chemie (International ed. in English), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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Who cites it
8 citing papers in PubMed.
- Stereoselective syntheses of 2-methyl-1,3-diol acetalsChemical science · 2023Article
- A Formal Rearrangement of Allylic Silanols.Molecules (Basel, Switzerland) · 2021Article
- Dictating Thermodynamic Control through Tethering: Applications to Stereoselective Bis-Spiroketal Synthesis.Angewandte Chemie (International ed. in English) · 2020Article
- ReOrganic letters · 2019Article
- Diarylmethane synthesis through ReChemical science · 2018Article
- ReAngewandte Chemie (International ed. in English) · 2017Article
- Evolution of a Unified Strategy for Complex Sesterterpenoids: Progress toward Astellatol and the Total Synthesis of (-)-Nitidasin.Chemistry (Weinheim an der Bergstrasse, Germany) · 2015Article
- Re2O7-catalyzed reaction of hemiacetals and aldehydes with O-, S-, and C-nucleophiles.Beilstein journal of organic chemistry · 2013Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Complexity from simplicity: polycyclic ethers are synthesized by cascade reactions involving the use of epoxides as electrophilic traps in the transposition of allylic alcohols. Stereogenic centers are created by functionalizing prochiral sites under thermodynamic control, and remote stereoinduction can be achieved through the use of ketones as conduits.
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Registered trials
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