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Volumn 52, Issue 10, 2011, Pages 1124-1127

Gold-mediated synthesis of α-ionone

Author keywords

Gold catalysis; Ionone; Meyer Schuster rearrangement; NHC; Propargylic esters

Indexed keywords

ALPHA IONONE; BENZOIC ACID; GOLD;

EID: 79551686982     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.01.010     Document Type: Article
Times cited : (26)

References (46)
  • 28
    • 51049121927 scopus 로고    scopus 로고
    • For a selection of recent reviews, see: Z. Li, C. Brouwer, and C. He Chem. Rev. 108 2008 3239 3265
    • (2008) Chem. Rev. , vol.108 , pp. 3239-3265
    • Li, Z.1    Brouwer, C.2    He, C.3
  • 29
    • 51249100498 scopus 로고    scopus 로고
    • A. Arcadi Chem. Rev. 108 2008 3266 3325
    • (2008) Chem. Rev. , vol.108 , pp. 3266-3325
    • Arcadi, A.1
  • 39
    • 77955683408 scopus 로고    scopus 로고
    • note
    • We are well aware that, in principle, the direct Meyer-Schuster rearrangement of propargylic alcohol 4a could yield the expected enone 1; however, under our conditions, a complex mixture was obtained, containing also an unidentified product, which is under investigation in our laboratories. For a recent application of the Meyer-Schuster rearrangement to the synthesis of natural products, see: Ramón, R. S.; Gaillard, S.; Slawin, A. M. Z.; Porta, A.; D'Alfonso, A.; Zanoni, G.; Nolan, S. P. Organometallics 2010, 29, 3665-3668.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.