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Volumn 63, Issue 27, 2007, Pages 6170-6181

Synthesis of 2,6-dimethyl-9-aryl-9-phosphabicyclo[3.3.1]nonanes: their application to asymmetric synthesis of chiral tetrahydroquinolines and relatives

Author keywords

Asymmetric cyclization; Chiral phosphine; Palladium catalyzed allylic amination; Tetrahydroquinoline

Indexed keywords

CYCLOOCTANE DERIVATIVE; NONANE;

EID: 34249019489     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.03.078     Document Type: Article
Times cited : (37)

References (66)
  • 7
    • 34249044800 scopus 로고    scopus 로고
    • For recent reviews on asymmetric allylic alkylation, see:
  • 10
    • 34249005903 scopus 로고    scopus 로고
    • note
    • (S)- and (R)- Designation in the (S)- and (R)-PBNs represent the stereochemistry of the ring juncture in the 9-phosphabicyclo[3.3.1]nonane skeleton for convenience' sake.
  • 12
    • 34249064191 scopus 로고    scopus 로고
    • For synthesis of martinelline and martinellic acids, see:
  • 23
    • 34248997472 scopus 로고    scopus 로고
    • For synthesis of tetrahydroquinoline skeleton, see:
  • 49
    • 34249074760 scopus 로고    scopus 로고
    • note
    • Commercial 1,5-dimethyl-1,5-cyclooctadiene (Aldrich Chemical Co.) was found to be a mixture of 1,5-dimethyl-1,5-cyclooctadiene and 1,6-dimethyl-1,5-cyclooctadiene in the ratio of 4/1, which was used without any further purification.
  • 55
    • 34249039568 scopus 로고    scopus 로고
    • For cyclization through palladium-catalyzed allylic alkylation, see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.