Cycloaromatization and DNA Cleavage of Novel Enyne-allene Systems

DOI: 10.1039/c39930001406

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1406 - 1407 (1993)

Update date:2022-08-03

Topics: Yield NMR spectroscopy Isolation Reaction Conditions DNA Cleavage

Authors:

Toshima, Kazunobu

Ohta, Kazumi

Ohtsuka, Atsuo

Matsumura, Shuichi

Nakata, Masaya

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Article abstract of DOI:10.1039/c39930001406

The novel enyne-allene sulfones 5-8 were prepared by m-chloroperbenzoic acid oxidation of the corresponding enediyne sulfides 1-4; the enyne-allene sulfones 6-8 having a leaving group at the allylic position were aromatized by 1,8-diazabicyclo<5.4.0>undec

Full text of DOI:10.1039/c39930001406

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