메뉴 건너뛰기




Volumn 130, Issue 51, 2008, Pages 17268-17269

Copper-catalyzed reaction of a-aryldiazoesters with terminal alkynes: A formal [3 + 2] cycloaddition route leading to indene derivatives

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE INSERTIONS; AROMATIC RINGS; CARBENOID; CATALYZED REACTIONS; CHEMO-SELECTIVITY; COPPER-CATALYZED REACTIONS; INTRAMOLECULAR ELECTROPHILIC ATTACK; REACTION CONDITIONS; TANDEM PROCESS; TERMINAL ALKYNE;

EID: 67849132887     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja808080h     Document Type: Article
Times cited : (89)

References (34)
  • 6
    • 67849109233 scopus 로고    scopus 로고
    • For recent examples of the asymmetric insertions, see
    • For recent examples of the asymmetric insertions, see:
  • 17
    • 0026544033 scopus 로고    scopus 로고
    • Davies et al. reported a Rh-catalyzed [3 + 2] cycloaddition reaction between vinyl ethers and a-vinyldiazoacetates, which affords cyclopentene adducts:(a) Davies. H. M. L.; Hu, B. Tetrahedron Lett. 1992, 33, 453.
    • Davies et al. reported a Rh-catalyzed [3 + 2] cycloaddition reaction between vinyl ethers and a-vinyldiazoacetates, which affords cyclopentene adducts:(a) Davies. H. M. L.; Hu, B. Tetrahedron Lett. 1992, 33, 453.
  • 21
    • 33749168701 scopus 로고    scopus 로고
    • For a previous report on the Cu-catalvzed cyclization reaction from this laboratory, see: Chans, S.; Lee, M.; Jung, D' Y.; Yoo, E. J.; Cho, S. H.; Han, S. K. J. Am Chem. Soc. 2006, 128, 12366.
    • For a previous report on the Cu-catalvzed cyclization reaction from this laboratory, see: Chans, S.; Lee, M.; Jung, D' Y.; Yoo, E. J.; Cho, S. H.; Han, S. K. J. Am Chem. Soc. 2006, 128, 12366.
  • 26
    • 67849087962 scopus 로고    scopus 로고
    • See the Supporting Information for details
    • See the Supporting Information for details.
  • 27
    • 67849123561 scopus 로고    scopus 로고
    • Employment of 1,2-disubstituted acetylenes afforded only cyclopropene compounds in high yields under the optimized conditions
    • Employment of 1,2-disubstituted acetylenes afforded only cyclopropene compounds in high yields under the optimized conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.