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Volumn 352, Issue 17, 2010, Pages 2899-2904

The first decarbonylative coupling of aldehydes and norbornenes catalyzed by rhodium

Author keywords

aldehydes; decarbonylative coupling; norbornenes; rhodium catalysis

Indexed keywords


EID: 78649556341     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201000476     Document Type: Article
Times cited : (49)

References (54)
  • 4
    • 78649556842 scopus 로고    scopus 로고
    • For examples, see
    • For examples, see
  • 11
    • 78649593184 scopus 로고    scopus 로고
    • For excellent reviews, see
    • For excellent reviews, see
  • 16
    • 77954555264 scopus 로고    scopus 로고
    • For a highlight of our work, see
    • X. Guo, J. Wang, C.-J. Li, Org. Lett. 2010, 12, 3176. For a highlight of our work, see
    • (2010) Org. Lett. , vol.12 , pp. 3176
    • Guo, X.1    Wang, J.2    Li, C.-J.3
  • 18
    • 77749283492 scopus 로고    scopus 로고
    • For an aldehyde decarbonylative arene-arene coupling, see
    • Angew. Chem. Int. Ed. 2010, 49, 1724. For an aldehyde decarbonylative arene-arene coupling, see
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 1724
  • 19
    • 77956247025 scopus 로고    scopus 로고
    • For aldehyde-decarbonylative conjugate addition and Heck-type reaction, see
    • Q. Shuai, L. Yang, X. Guo, O. Basle, C.-J. Li, J. Am. Chem. Soc. 2010, 132, 12212. For aldehyde-decarbonylative conjugate addition and Heck-type reaction, see
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 12212
    • Shuai, Q.1    Yang, L.2    Guo, X.3    Basle, O.4    Li, C.-J.5
  • 21
    • 33746588234 scopus 로고    scopus 로고
    • Varela et al. reported an alternative ruthenium-catalyzed formation of cyclic alkenes from aldehydes and alkynes via the cleavage of C≡C bonds see:,. For pioneering work on ruthenium-catalyzed decarbonylations, see
    • Varela et al. reported an alternative ruthenium-catalyzed formation of cyclic alkenes from aldehydes and alkynes via the cleavage of C≡C bonds see:, J. A. Varela, C. Gonzales-Rodriguez, S. G. Rubin, L. Castedo, C. Saa, J. Am. Chem. Soc. 2006, 128, 9576. For pioneering work on ruthenium-catalyzed decarbonylations, see
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 9576
    • Varela, J.A.1    Gonzales-Rodriguez, C.2    Rubin, S.G.3    Castedo, L.4    Saa, C.5
  • 25
    • 78649550935 scopus 로고    scopus 로고
    • For examples of transition metal-catalyzed arylation of norbornenes with organometallic reagents, see
    • For examples of transition metal-catalyzed arylation of norbornenes with organometallic reagents, see
  • 32
    • 78649564918 scopus 로고    scopus 로고
    • The excess amount of norbornene was used to compensate its loss due to its evaporation during the reaction
    • The excess amount of norbornene was used to compensate its loss due to its evaporation during the reaction.
  • 33
    • 78649541664 scopus 로고    scopus 로고
    • For examples of decarboxylative coupling of carboxylic acid derivatives, see
    • For examples of decarboxylative coupling of carboxylic acid derivatives, see
  • 54
    • 78649550452 scopus 로고    scopus 로고
    • 3 (214.8mg, 0.60mmol, 10mol%), vacuumed and refilled with argon. Then toluene (6mL) was added under argon protection and the autoclave was sealed and heated at 150°C (oil bath temperature) for 24h. The decarbonylative coupling product 6d was isolated in 80% (1.032g) yield and the reduced yield may be caused by the accumulation of CO in the autoclave
    • 3 (214.8mg, 0.60mmol, 10mol%), vacuumed and refilled with argon. Then toluene (6mL) was added under argon protection and the autoclave was sealed and heated at 150°C (oil bath temperature) for 24h. The decarbonylative coupling product 6d was isolated in 80% (1.032g) yield and the reduced yield may be caused by the accumulation of CO in the autoclave.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.