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Volumn 12, Issue 20, 2010, Pages 4435-4437

Exclusive photodimerization reactions of chromone-2-carboxylic esters depending on reaction media

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EID: 77957836567     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101734k     Document Type: Article
Times cited : (26)

References (22)
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    • 85020071329 scopus 로고    scopus 로고
    • Inoue, Y.; Ramamurthy, V., Eds.; Marcel Dekker: New York
    • Inoue, Y. In Chiral Photochemistry; Inoue, Y.; Ramamurthy, V., Eds.; Marcel Dekker: New York, 2004; Vol. 11, pp 129 - 177.
    • (2004) Chiral Photochemistry , vol.11 , pp. 129-177
    • Inoue, Y.1
  • 3
    • 84988543340 scopus 로고    scopus 로고
    • Inoue, Y.; Ramamurthy, V., Eds.; Marcel Dekker: New York
    • Grosch, B.; Bach, T. In Chiral Photochemistry; Inoue, Y.; Ramamurthy, V., Eds.; Marcel Dekker: New York, 2004; Vol. 11, pp 315 - 340.
    • (2004) Chiral Photochemistry , vol.11 , pp. 315-340
    • Grosch, B.1
  • 4
    • 84979609583 scopus 로고    scopus 로고
    • Inoue, Y.; Ramamurthy, V., Eds.; Marcel Dekker: New York
    • Sakamoto, M. In Chiral Photochemistry; Inoue, Y.; Ramamurthy, V., Eds.; Marcel Dekker: New York, 2004; Vol. 11, pp 415 - 461.
    • (2004) Chiral Photochemistry , vol.11 , pp. 415-461
    • Sakamoto, M.1
  • 16
    • 65349093967 scopus 로고    scopus 로고
    • Photodimerization of a simple chromone leading to anti -HT and cis - trans -HT dimers in low quantum efficiency.
    • Photodimerization of a simple chromone leading to anti -HT and cis-trans -HT dimers in low quantum efficiency. Sakamoto, M.; Kanehiro, M.; Mino, T.; Fujita, T. Chem. Commun. 2009, 2379-2380
    • (2009) Chem. Commun. , pp. 2379-2380
    • Sakamoto, M.1    Kanehiro, M.2    Mino, T.3    Fujita, T.4
  • 17
    • 77957825125 scopus 로고    scopus 로고
    • Photodimerization of 3-methoxychromone derivatives subsequently followed by Norrish Type II reaction, in which the stereochemistry and the details are ambiguous
    • Photodimerization of 3-methoxychromone derivatives subsequently followed by Norrish Type II reaction, in which the stereochemistry and the details are ambiguous


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