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Volumn 71, Issue 7, 2006, Pages 2914-2917

An unexpectedly mild thermal Alder-ene-type cyclization of enallenes

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; BYPRODUCTS; CATALYSTS; CHEMICAL BONDS; CHEMICAL REACTIONS; WASTES;

EID: 33645502322     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo060013g     Document Type: Article
Times cited : (27)

References (32)
  • 13
    • 22944485617 scopus 로고    scopus 로고
    • (b) Ma, S. Chem. Rev. 2005, 105, 2829.
    • (2005) Chem. Rev. , vol.105 , pp. 2829
    • Ma, S.1
  • 26
    • 33645532139 scopus 로고    scopus 로고
    • note
    • The acyclic substrate 1i was synthesized from an acyclic allylic acetate. For synthesis of enallene substrates 1e and 1f, see ref 6.
  • 27
    • 33645505032 scopus 로고    scopus 로고
    • note
    • The stereochemistry of trans-2g and cis-2g was assigned by NOE measurements.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.