Synthesis of chiral 1,3-diols by radical-mediated regioselective opening of 2,3-epoxy alcohols using cp2TiCl
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
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2. Taylor, S. K. Tetrahedron 2000, 56, 1149−1163. It is not possible to list all the references here. However, a quick search in http://organic.chemweb.com under ‘ring opening of epoxides’ will provide a complete list of relevant references.
3. Anti-Markovnikov opening of trisubstituted epoxy alcohols: application in the synthesis of 2-methyl-1,3-diols
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5. Diastereoselective opening of trisubstituted epoxy alcohols: application in the synthesis of (+)-prelactone C
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2. A Tandem Semipinacol Rearrangement/Aldehyde Arylation or Alkylation of Trisubstituted 2,3-Epoxy Alcohols with Grignard Reagents for Functionalized 1,3-Diols;The Journal of Organic Chemistry;2022-06-09
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