Enantioselective total synthesis of heliannuols D and A

Kenya Takabatake, Izumi Nishi, Mitsuru Shindo, Kozo Shishido

Research output: Contribution to journalArticle

59 Citations (Scopus)

Abstract

Heliannuols D and A, which exhibit allelopathic activity, were synthesized enantioselectively via a base-mediated intramolecular cyclisation of a phenolic epoxide for the first time, and the absolute structures were established by total synthesis.

Original languageEnglish
Pages (from-to)1807-1808
Number of pages2
JournalJournal of the Chemical Society, Perkin Transactions 1
Issue number12
DOIs
Publication statusPublished - 2000
Externally publishedYes

Fingerprint

Cyclization
Epoxy Compounds
heliannuol D
heliannuol A

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Enantioselective total synthesis of heliannuols D and A. / Takabatake, Kenya; Nishi, Izumi; Shindo, Mitsuru; Shishido, Kozo.

In: Journal of the Chemical Society, Perkin Transactions 1, No. 12, 2000, p. 1807-1808.

Research output: Contribution to journalArticle

Takabatake, Kenya ; Nishi, Izumi ; Shindo, Mitsuru ; Shishido, Kozo. / Enantioselective total synthesis of heliannuols D and A. In: Journal of the Chemical Society, Perkin Transactions 1. 2000 ; No. 12. pp. 1807-1808.
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