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Volumn 10, Issue 1, 2012, Pages 70-78

Indolizinones as synthetic scaffolds: Fundamental reactivity and the relay of stereochemical information

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREOSELECTIVE HYDROGENATION; DIELS-ALDER CYCLOADDITIONS; ENE REACTION; FIVE-MEMBERED RINGS; INDOLIZINONES; N-HETEROCYCLES; NATURAL PRODUCT SYNTHESIS; SELECTIVE HYDROGENATION; STEREOCENTERS; SYNTHETIC SCAFFOLDS;

EID: 82955240842     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob06423a     Document Type: Article
Times cited : (35)

References (17)
  • 6
    • 34548158479 scopus 로고    scopus 로고
    • The cyclization of tertiary alcohols such as 5 in water to obtain indolizinone products was developed in our laboratories concurrently with Kim and coworkers' (see ref. 5) report of the EtOH version of this metal-free reaction
    • I. V. Seregin A. W. Schammel V. Gevorgyan Org. Lett. 2007 9 3433 3436
    • (2007) Org. Lett. , vol.9 , pp. 3433-3436
    • Seregin, I.V.1    Schammel, A.W.2    Gevorgyan, V.3
  • 9
    • 0003979828 scopus 로고    scopus 로고
    • Academic Press, London
    • R. J. Sundberg, Indoles, Academic Press, London, 1996
    • (1996) Indoles
    • Sundberg, R.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.