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Volumn 67, Issue 48, 2011, Pages 9401-9404

Expedient synthesis of 4-O-methylhonokiol via Suzuki-Miyaura cross-coupling

Author keywords

4 O Methylhonokiol; Neolignan; Potassium aryltrifluoroborate; Suzuki Miyaura cross coupling

Indexed keywords

4 O METHYLHONOKIOL; HONOKIOL; PHENOL DERIVATIVE; RUTHENIUM; UNCLASSIFIED DRUG;

EID: 80054850043     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.09.115     Document Type: Article
Times cited : (15)

References (28)
  • 11
    • 79954606182 scopus 로고    scopus 로고
    • During preparation of this manuscript, a concise synthesis of 4-O-methyl honokiol was reported, see
    • During preparation of this manuscript, a concise synthesis of 4-O-methyl honokiol was reported, see: Denton, R. M.; Scragg, J. T.; Saska, J. Tetrahedron Lett. 2011, 52, 2554-2556.
    • (2011) Tetrahedron Lett. , vol.52 , pp. 2554-2556
    • Denton, R.M.1    Scragg, J.T.2    Saska, J.3
  • 23
    • 80054866336 scopus 로고    scopus 로고
    • note
    • For examples of the preparation of 2-bromo-4-allylphenol, see: WO 2006107451. For related example of the preparation of 2-bromo-4-allylanisole, see Ref. 3.
  • 25
    • 4644298316 scopus 로고    scopus 로고
    • Although 2-allyl-4-bromoanisole 7 is known, it was prepared by allylation of commerciallyl available 4-bromophenol (97%), Claisen rearrangement (84%), and methylation (94%). For allylation and rearrangement, see
    • Although 2-allyl-4-bromoanisole 7 is known, it was prepared by allylation of commerciallyl available 4-bromophenol (97%), Claisen rearrangement (84%), and methylation (94%). For allylation and rearrangement, see: Bujok, R.; Bieniek, M.; Masnyk, M.; Michrowska, A.; Sarosiek, A.; Stȩpowska, H.; Arlt, D.; Grela, K. J. Org. Chem. 2004, 69, 6894-6896.
    • (2004) J. Org. Chem. , vol.69 , pp. 6894-6896
    • Bujok, R.1    Bieniek, M.2    Masnyk, M.3    Michrowska, A.4    Sarosiek, A.5    Stȩpowska, H.6    Arlt, D.7    Grela, K.8
  • 27
    • 0035813437 scopus 로고    scopus 로고
    • For examples of the SuzukieMiyura reaction in the presence of the unprotected phenol, see
    • For examples of the SuzukieMiyura reaction in the presence of the unprotected phenol, see: (a) Zhuravel, M. A.; Nguyen, S. T. Tetrahedron Lett. 2001, 42, 7925-7928;
    • (2001) Tetrahedron Lett. , vol.42 , pp. 7925-7928
    • Zhuravel, M.A.1    Nguyen, S.T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.