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Volumn 126, Issue 10, 2004, Pages 3036-3037

Deuterium-Labeling Studies Establishing Stereochemistry at the Oxypalladation Step in Wacker-Type Oxidative Cyclization of an o-Allylphenol

Author keywords

[No Author keywords available]

Indexed keywords

DEUTERIUM; O ALLYLPHENOL; PHENOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 1642300603     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja031946m     Document Type: Article
Times cited : (116)

References (32)
  • 1
    • 0003441482 scopus 로고
    • John Wiley and Sons: Chichester
    • For reviews: (a) Tsuji, J. Palladium Reagents and Catalysts; John Wiley and Sons: Chichester, 1995; pp 19-124.
    • (1995) Palladium Reagents and Catalysts , pp. 19-124
    • Tsuji, J.1
  • 22
    • 0037951429 scopus 로고    scopus 로고
    • For recent reports on the deuterium-labeling studies on the mechanism of palladium-catalyzed reactions: (a) Franzén, J.; Bäckvall, J.-E. J. Am. Chem. Soc. 2003, 125, 6056.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 6056
    • Franzén, J.1    Bäckvall, J.-E.2
  • 28
    • 1642332331 scopus 로고    scopus 로고
    • note
    • At 42% conversion, recovered cis-1 was 10% ee, indicating that a low level of kinetic resolution (S = 1.4) took place. In the absence of the boxax ligand, the reaction gave a considerable amount of 1-(2-hydroxyphenyl)-1-methoxycyclohexane together with a low yield (total 33%) of a mixture of the tetrahydrobenzofurans.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.