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Volumn 32, Issue 3, 2011, Pages 1087-1090

Remarkable rate acceleration of baylis-hillman reaction of notorious α,β-unsaturated aldehydes catalyzed by proton donor

Author keywords

, Unsaturated aldehydes; Baylis hillman reaction; Phenol; Proton donor

Indexed keywords


EID: 79953268366     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2011.32.3.1087     Document Type: Article
Times cited : (7)

References (46)
  • 1
    • 0037366617 scopus 로고    scopus 로고
    • For the leading reviews on Baylis-Hillman reaction, see
    • For the leading reviews on Baylis-Hillman reaction, see: Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891.
    • (2003) Chem. Rev. , vol.103 , pp. 811-891
    • Basavaiah, D.1    Rao, A.J.2    Satyanarayana, T.3
  • 8
    • 77956464073 scopus 로고    scopus 로고
    • and further references cited therein
    • Basavaiah, D.; Reddy, B. S.; Badsara, S. S. Chem. Rev. 2010, 110, 5447-5674 and further references cited therein.
    • (2010) Chem. Rev. , vol.110 , pp. 5447-5674
    • Basavaiah, D.1    Reddy, B.S.2    Badsara, S.S.3
  • 9
    • 70349769318 scopus 로고    scopus 로고
    • For the synthesis of Baylis-Hillman adducts of cinnamaldehyde derivatives, see
    • For the synthesis of Baylis-Hillman adducts of cinnamaldehyde derivatives, see: Song, Y.; Ke, H.; Wang, N.; Wang, L.; Zou, G. Tetrahedron 2009, 65, 9086-9090.
    • (2009) Tetrahedron , vol.65 , pp. 9086-9090
    • Song, Y.1    Ke, H.2    Wang, N.3    Wang, L.4    Zou, G.5
  • 16
    • 0035823312 scopus 로고    scopus 로고
    • For the use of special acrylates in order to increase the reaction rate, see
    • For the use of special acrylates in order to increase the reaction rate, see: Lee, W.-D.; Yang, K.-S.; Chen, K. Chem. Commun. 2001, 1612-1613.
    • (2001) Chem. Commun. , pp. 1612-1613
    • Lee, W.-D.1    Yang, K.-S.2    Chen, K.3
  • 22
    • 79953288784 scopus 로고    scopus 로고
    • The manuscript on palladium-catalyzed synthesis of cyclobuta- [a]indene scaffold from the modified Baylis-Hillman adducts of cinnamaldehydes will be published in due course
    • The manuscript on palladium-catalyzed synthesis of cyclobuta- [a]indene scaffold from the modified Baylis-Hillman adducts of cinnamaldehydes will be published in due course.
  • 23
    • 0742322001 scopus 로고    scopus 로고
    • For the rate increase by proton donor additive in DABCOcatalyzed Baylis-Hillman reactions, see
    • For the rate increase by proton donor additive in DABCOcatalyzed Baylis-Hillman reactions, see: Maher, D. J.; Connon, S. J. Tetrahedron Lett. 2004, 45, 1301-1305.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 1301-1305
    • Maher, D.J.1    Connon, S.J.2
  • 31
    • 0000516236 scopus 로고    scopus 로고
    • Various Lewis acids have also been used for the same purpose, see
    • Various Lewis acids have also been used for the same purpose, see: Aggarwal, V. K.; Mereu, A.; Tarver, G. J.; McCague, R. J. Org. Chem. 1998, 63, 7183-7189.
    • (1998) J. Org. Chem. , vol.63 , pp. 7183-7189
    • Aggarwal, V.K.1    Mereu, A.2    Tarver, G.J.3    McCague, R.4
  • 34
    • 33744469835 scopus 로고    scopus 로고
    • For the rate increase by proton donor additive in phosphine or other Lewis base-catalyzed Baylis-Hillman reactions, see
    • For the rate increase by proton donor additive in phosphine or other Lewis base-catalyzed Baylis-Hillman reactions, see: Shi, M.; Liu, Y.-H. Org. Biomol. Chem. 2006, 1468-1470.
    • (2006) Org. Biomol. Chem. , pp. 1468-1470
    • Shi, M.1    Liu, Y.-H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.