메뉴 건너뛰기




Volumn 37, Issue 8, 1996, Pages 1321-1324

π-Facial diastereoselectivity in electrophilic additions and 1,3-dipolar cycloadditions to bicyclo[2.2.2]oct-2-enes 5,6-cis,exo-disubstituted with electron withdrawing groups

Author keywords

[No Author keywords available]

Indexed keywords

BICYCLO[2.2.2]OCTANE DERIVATIVE;

EID: 0030022283     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(95)02384-4     Document Type: Article
Times cited : (10)

References (26)
  • 3
    • 85030195837 scopus 로고    scopus 로고
    • ch. 12
    • (c) Mander, L. N. Stereoselective Synthesis, ch. 12 in Eliel, E. E.; Wilen, S. H. Stereochemistry of Organic Compounds, Wiley-Interscience, New York, 1994.
    • Stereoselective Synthesis
    • Mander, L.N.1
  • 22
    • 85030190600 scopus 로고    scopus 로고
    • note
    • Moreover the syn and and transition structures (both AM1 and STO-3G) of the reaction of HCNO with 1 f clearly show that the allylic anti σ bonds bear an almost exact antiperiplanar relationship to the incipient bonds. That is, at least in 1,3-dipolar cycloadditions, Cieplak's effect should be at its maximum.
  • 26
    • 85030188106 scopus 로고    scopus 로고
    • note
    • 8H bridge.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.