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Volumn 122, Issue 31, 2000, Pages 7604-7605

Highly enantioselective palladium(II)-catalyzed cyclization of (Z)-4'-acetoxy-2'-butenyl 2-alkynoates: An efficient synthesis of optically active γ-butyrolactones [7]

Author keywords

[No Author keywords available]

Indexed keywords

PALLADIUM;

EID: 0034625935     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja001379s     Document Type: Letter
Times cited : (151)

References (32)
  • 9
    • 0033517049 scopus 로고    scopus 로고
    • and references therein
    • Notable examples include allylic substitution and Heck reaction: (a) Tenaglia, A.; Heumann, A. Angew. Chem., Int. Ed. 1999, 38, 2180 and references therein. (b) Tsuji, J. Palladium Reagents and Catalysis: Innovations in Organic Synthesis; John Wiley & Sons: Chichester, 1995.
    • (1999) Angew. Chem., Int. Ed. , vol.38 , pp. 2180
    • Tenaglia, A.1    Heumann, A.2
  • 10
    • 0033517049 scopus 로고    scopus 로고
    • John Wiley & Sons: Chichester
    • Notable examples include allylic substitution and Heck reaction: (a) Tenaglia, A.; Heumann, A. Angew. Chem., Int. Ed. 1999, 38, 2180 and references therein. (b) Tsuji, J. Palladium Reagents and Catalysis: Innovations in Organic Synthesis; John Wiley & Sons: Chichester, 1995.
    • (1995) Palladium Reagents and Catalysis: Innovations in Organic Synthesis
    • Tsuji, J.1
  • 23
    • 12944271042 scopus 로고    scopus 로고
    • note
    • 3·CHCli, no desired cyclization product 2a was obtained.
  • 24
    • 12944282281 scopus 로고    scopus 로고
    • note
    • It should be noted that the corresponding reactions of propiolate ester and (E)-4′-acetoxy-2′-bulenyl 2-alkynoates did not occur.
  • 28
  • 30
    • 12944310368 scopus 로고    scopus 로고
    • note
    • D +12.7°).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.