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Volumn 61, Issue 6, 1996, Pages 2031-2037

Structure and asymmetric diels-alder reactions of optically active allene-1,3-dicarboxylates

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CONFIGURATION; CHEMICAL TRANSFORMATIONS; CYCLOPENTADIENES; DICARBOXYLATES; DIELS-ALDER REACTION; DIENOPHILES; OPTICALLY ACTIVE; ORBITAL INTERACTION;

EID: 0000045397     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo951762t     Document Type: Article
Times cited : (39)

References (36)
  • 12
    • 0000101901 scopus 로고
    • and references cited therein
    • (i) Marshall, J. A.; Wang, X.-J. J. Org. Chem. 1992, 57, 2747, and references cited therein.
    • (1992) J. Org. Chem , vol.57 , pp. 2747
    • Marshall, J.A.1    Wang, X.-J.2
  • 13
    • 76049119179 scopus 로고
    • (j) Idem. Ibid. 1992, 57, 1242.
    • (1992) Idem. Ibid , vol.57 , pp. 1242
  • 23
  • 27
    • 76049105818 scopus 로고    scopus 로고
    • Patai, S., Ed. The Chemistry of Ketenes, Allenes, and Related Compounds; John Wiley & Sons, Inc.: Chichester, 1980; Part 1 and 2.
    • Patai, S., Ed. The Chemistry of Ketenes, Allenes, and Related Compounds; John Wiley & Sons, Inc.: Chichester, 1980; Part 1 and 2.
  • 29
    • 85016612531 scopus 로고    scopus 로고
    • Allinger, N. L.; Zhou, X.; Bergsma, J. J. Mol. Struct. 1994, 312-(118), 69.
    • Allinger, N. L.; Zhou, X.; Bergsma, J. J. Mol. Struct. 1994, 312-(118), 69.
  • 32
    • 76049096970 scopus 로고    scopus 로고
    • The Lewis acid-catalyzed Diels-Alder reaction of 1a with diphenylfulvene only led to polymerization although the uncatalyzed reaction (benzene, 60°C) gave the exo adduct (68 %) and the endo adduct (32%).
    • The Lewis acid-catalyzed Diels-Alder reaction of 1a with diphenylfulvene only led to polymerization although the uncatalyzed reaction (benzene, 60°C) gave the exo adduct (68 %) and the endo adduct (32%).
  • 36
    • 76049110166 scopus 로고    scopus 로고
    • The author has deposited atomic coordinates for this structure with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK
    • The author has deposited atomic coordinates for this structure with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.