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Volumn 129, Issue 12, 2007, Pages 3520-3521

Enantioselective, cyclopentene-forming annulations via NHC-catalyzed benzoin-oxy-Cope reactions

Author keywords

[No Author keywords available]

Indexed keywords

BENZOIN; CYCLOPENTENE DERIVATIVE;

EID: 33947696588     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0705543     Document Type: Article
Times cited : (292)

References (36)
  • 6
    • 33644764723 scopus 로고    scopus 로고
    • (c) Zeitler, K. Org. Lett. 2006, 8, 637-640.
    • (2006) Org. Lett , vol.8 , pp. 637-640
    • Zeitler, K.1
  • 15
    • 0034829401 scopus 로고    scopus 로고
    • For elegant intermolecular, catalytic enantioselective approaches to chiral cyclopentenes, see: a
    • For elegant intermolecular, catalytic enantioselective approaches to chiral cyclopentenes, see: (a) Davies, H. M. L.; Xiang, B.; Kong, N.; Stafford, D. G. J. Am. Chem. Soc. 2001, 123, 7461-7462.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 7461-7462
    • Davies, H.M.L.1    Xiang, B.2    Kong, N.3    Stafford, D.G.4
  • 17
    • 33749027460 scopus 로고    scopus 로고
    • Romo has reported that [3.2.0]-bicyclic β-lactones bearing aliphatic substituents do not undergo spontaneous decarboxylation: Henry-Riyad, H.; Lee, C.; Purohit, V. C.; Romo, D. Org. Lett. 2006, 8, 4363-4366.
    • Romo has reported that [3.2.0]-bicyclic β-lactones bearing aliphatic substituents do not undergo spontaneous decarboxylation: Henry-Riyad, H.; Lee, C.; Purohit, V. C.; Romo, D. Org. Lett. 2006, 8, 4363-4366.
  • 26
    • 0038001592 scopus 로고    scopus 로고
    • Products arising from retro-silyl benzoin reactions and those of silyl Stetter reactions of these products were also detected. For reports of silyl benzoin and Stetter reactions, see: (a) Linghu, X, Johnson, J. S. Angew. Chem, Int. Ed. 2003, 42, 2534-2536
    • Products arising from retro-silyl benzoin reactions and those of silyl Stetter reactions of these products were also detected. For reports of silyl benzoin and Stetter reactions, see: (a) Linghu, X.; Johnson, J. S. Angew. Chem., Int. Ed. 2003, 42, 2534-2536.
  • 29
    • 4444242684 scopus 로고    scopus 로고
    • For concerted C-H insertion/Cope rearrangement reactions, see: (a) Davies, H. M. L.; Jin, Q. J. Am. Chem. Soc. 2004, 126, 10862-10863.
    • For concerted C-H insertion/Cope rearrangement reactions, see: (a) Davies, H. M. L.; Jin, Q. J. Am. Chem. Soc. 2004, 126, 10862-10863.
  • 35
    • 0000448986 scopus 로고    scopus 로고
    • Both chair and boat conformations are invoked in the transition states of oxy-Cope rearrangements to explain the observed stereochemical outcomes: (a) Evans, D. A, Nelson, J. V. J. Am. Chem. Soc. 1980, 102, 774-782
    • Both chair and boat conformations are invoked in the transition states of oxy-Cope rearrangements to explain the observed stereochemical outcomes: (a) Evans, D. A.; Nelson, J. V. J. Am. Chem. Soc. 1980, 102, 774-782.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.