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Volumn 64, Issue 21, 1999, Pages 7846-7855

Studies on the synthesis of aza analogues of illudins by cycloadditions to highly strained methylenecyclopropanes

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANE DERIVATIVE; HETEROCYCLIC COMPOUND; ILLUDIN M; ILLUDIN S;

EID: 0032740781     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo990873f     Document Type: Article
Times cited : (48)

References (59)
  • 10
    • 33847511978 scopus 로고    scopus 로고
    • de Meijere, A., Ed.; Thieme, Stuttgart, Chapters 5.2.2 and 5.2.3.
    • (b) Houben-Weyl, Carbocyclic Three-Membered Ring Compounds; de Meijere, A., Ed.; Thieme, Stuttgart, 1997; Vol. E 17c, Chapters 5.2.2 and 5.2.3.
    • (1997) Carbocyclic Three-Membered Ring Compounds , vol.E 17C
    • Houben-Weyl1
  • 36
    • 0001487604 scopus 로고    scopus 로고
    • For reviews on the synthesis of alkylidenecyclopropanes see: (a) Brandi, A.; Goti, A. Chem. Rev. 1998, 98, 589.
    • (1998) Chem. Rev. , vol.98 , pp. 589
    • Brandi, A.1    Goti, A.2
  • 37
    • 33847499622 scopus 로고    scopus 로고
    • loc. cit (4).
    • (b) loc. cit (4).
  • 49
    • 33744701902 scopus 로고    scopus 로고
    • note
    • Ab initio STO 3G calculations for the FM Orbitals of nitrone 22, BCP 4, and MSP 7 were performed and showed that the dominant interaction was the LUMO (dipole)-HOMO (dipolarophile) for both alkenes, but the corresponding AE values were not significantly different.
  • 53
    • 0033591935 scopus 로고    scopus 로고
    • and references therein.
    • For a recent computational study of nitrone and nitrile oxide cycloadditions, see: Cossio, F. P.; Morao, I.; Jiao, H.; Schleyer, P. v. R. J. Am. Chem. Soc. 1999,121, 6737 and references therein.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6737
    • Cossio, F.P.1    Morao, I.2    Jiao, H.3    Schleyer, P.V.R.4
  • 59
    • 33847522188 scopus 로고    scopus 로고
    • Dissertation, Universität Göttingen
    • Faber, D. Dissertation, Universität Göttingen, 1996.
    • (1996)
    • Faber, D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.