Highly Enantioselective Epoxidation of 2,2-Dimethylchromenes

Akira Hatayama, Naoki Hosoya, Ryo Irie, Yoshio Ito, Tsutomu Katsuki

Research output: Contribution to journalArticle

32 Citations (Scopus)

Abstract

A newly synthesized chiral [bis(salicylidene)ethylenediamine]manganese(III) complex 2a was found to catalyze the epoxidation of 2,2-dimethylchromenes 15-17 with high enantioselectivity (86-92% ee).

Original languageEnglish
Pages (from-to)407-409
Number of pages3
JournalSynlett
Volume1992
Issue number5
DOIs
Publication statusPublished - May 1992

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ethylenediamine
Epoxidation
Enantioselectivity
Manganese

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Hatayama, A., Hosoya, N., Irie, R., Ito, Y., & Katsuki, T. (1992). Highly Enantioselective Epoxidation of 2,2-Dimethylchromenes. Synlett, 1992(5), 407-409. https://doi.org/10.1055/s-1992-21361

Highly Enantioselective Epoxidation of 2,2-Dimethylchromenes. / Hatayama, Akira; Hosoya, Naoki; Irie, Ryo; Ito, Yoshio; Katsuki, Tsutomu.

In: Synlett, Vol. 1992, No. 5, 05.1992, p. 407-409.

Research output: Contribution to journalArticle

Hatayama, A, Hosoya, N, Irie, R, Ito, Y & Katsuki, T 1992, 'Highly Enantioselective Epoxidation of 2,2-Dimethylchromenes', Synlett, vol. 1992, no. 5, pp. 407-409. https://doi.org/10.1055/s-1992-21361
Hatayama, Akira ; Hosoya, Naoki ; Irie, Ryo ; Ito, Yoshio ; Katsuki, Tsutomu. / Highly Enantioselective Epoxidation of 2,2-Dimethylchromenes. In: Synlett. 1992 ; Vol. 1992, No. 5. pp. 407-409.
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