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Volumn 43, Issue 9, 2014, Pages 2979-3002

Allene ether Nazarov cyclization

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALKADIENE; ALKOXYL RADICAL; ALKYNE; AMINE; BIOLOGICAL PRODUCT; CYCLOPENTANE DERIVATIVE; ETHER DERIVATIVE; IMINE; KETONE; OXIDE; PROPADIENE; PROPARGYL ETHER;

EID: 84896528449     PISSN: 03060012     EISSN: 14604744     Source Type: Journal    
DOI: 10.1039/c3cs60333d     Document Type: Review
Times cited : (178)

References (116)
  • 1
    • 33746062487 scopus 로고    scopus 로고
    • Cyclizations of Allenes
    • in, ed. N. Krause and A. S. K. Hashmi, Wiley-VCH, Weinheim, 2, 817-846 Reviews
    • M. A. Tius, Cyclizations of Allenes in Modern Allene Chemistry, ed., N. Krause, and, A. S. K. Hashmi, Wiley-VCH, Weinheim, 2004, vol. 2, pp. 817-846
    • (2004) Modern Allene Chemistry
    • Tius, M.A.1
  • 70
    • 55249095050 scopus 로고    scopus 로고
    • The release of steric compression caused by two adjacent OTBS groups at C3 and C4 is a well known effect
    • A. R. Banaag M. A. Tius J. Org. Chem. 2008 73 8133
    • (2008) J. Org. Chem. , vol.73 , pp. 8133
    • Banaag, A.R.1    Tius, M.A.2
  • 79
    • 34247898947 scopus 로고    scopus 로고
    • Lithioallene 91 was used as a 88/12 mixture of enantiomers, hence asymmetry transfer was approximately 11%
    • A. R. Banaag M. A. Tius J. Am. Chem. Soc. 2007 129 5328
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 5328
    • Banaag, A.R.1    Tius, M.A.2
  • 104
    • 0035953069 scopus 로고    scopus 로고
    • Relief of ring strain can also be used to drive an imino-Nazarov cyclization that would otherwise be unfavourable
    • M. A. Tius C. C. Chu R. Nieves-Colberg Tetrahedron Lett. 2001 42 2419
    • (2001) Tetrahedron Lett. , vol.42 , pp. 2419
    • Tius, M.A.1    Chu, C.C.2    Nieves-Colberg, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.