Photoreactions of dispiro{naphthalene-1,2′-naphtho[2,1-b]pyran- 3′,1″-naphthalene}-2(1H),2″(1″H)-dione. A novel case of β-C-C cleavage in an enone

Tirumalai R. Kasturi, Gonibella J. Raju, Vaidhyanathan Ramamurthy

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Irradiation of the title compound (2) gave a wide range of products, identified as compounds (3)-(7) on the basis of spectroscopic data and chemical evidence, which result from β-cleavages and intramolecular cycloaddition.

Original languageEnglish
Pages (from-to)557-559
Number of pages3
JournalJournal of the Chemical Society, Chemical Communications
Issue number11
StatePublished - Dec 1 1981
Externally publishedYes

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Cycloaddition
Cycloaddition Reaction
Irradiation
naphthalene
naphtho(2,1-b)pyran

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

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title = "Photoreactions of dispiro{naphthalene-1,2′-naphtho[2,1-b]pyran- 3′,1″-naphthalene}-2(1H),2″(1″H)-dione. A novel case of β-C-C cleavage in an enone",
abstract = "Irradiation of the title compound (2) gave a wide range of products, identified as compounds (3)-(7) on the basis of spectroscopic data and chemical evidence, which result from β-cleavages and intramolecular cycloaddition.",
author = "Kasturi, {Tirumalai R.} and Raju, {Gonibella J.} and Vaidhyanathan Ramamurthy",
year = "1981",
month = "12",
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journal = "Journal of the Chemical Society",
issn = "0577-6171",
publisher = "Chemical Society",
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AU - Kasturi, Tirumalai R.

AU - Raju, Gonibella J.

AU - Ramamurthy, Vaidhyanathan

PY - 1981/12/1

Y1 - 1981/12/1

N2 - Irradiation of the title compound (2) gave a wide range of products, identified as compounds (3)-(7) on the basis of spectroscopic data and chemical evidence, which result from β-cleavages and intramolecular cycloaddition.

AB - Irradiation of the title compound (2) gave a wide range of products, identified as compounds (3)-(7) on the basis of spectroscopic data and chemical evidence, which result from β-cleavages and intramolecular cycloaddition.

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