2(3H)-and 2(5H)-furanones. VII. Chirality transfer on the tetronic acid templates

Takefumi Momose, Naoki Toyooka*, Morihiro Nishio, Hiroyuki Shinoda, Hiromi Fujii, Hironobu Yanagino

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

The chirality transfer on the β-tetronic acid templates has been examined via highly diastereoselective alkylation or the Michael reaction at the α-position of the acids. Synthetic utility of this transfer procedure was demonstrated by the formal synthesis of (+)-cassiol and enantiodivergent synthesis of O-methyljoubertiamine.

Original languageEnglish
Pages (from-to)1321-1343
Number of pages23
JournalHeterocycles
Volume51
Issue number6
DOIs
StatePublished - 1999/06/01

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

Fingerprint

Dive into the research topics of '2(3H)-and 2(5H)-furanones. VII. Chirality transfer on the tetronic acid templates'. Together they form a unique fingerprint.

Cite this