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Volumn 50, Issue 31, 2009, Pages 4416-4419

Appending aromatic moieties at the para- and meta-position of calixarene phenol rings via p-bromodienone route

Author keywords

Calixarene exo rim; Dienone phenol rearrangement; Inherently chiral calixarenes; Meta substituted calixarenes; p Bromodienone route

Indexed keywords

ALKADIENE; CALIXARENE; CARBON; OXYGEN; PHENOL DERIVATIVE; SILVER;

EID: 66949125432     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.05.032     Document Type: Article
Times cited : (40)

References (50)
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    • For comprehensive reviews on calixarenes see:
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    • 4f For general reviews see Ref. 1, while for representative or recent examples, see:
    • 4f For general reviews see Ref. 1, while for representative or recent examples, see:. Shinkai S., Koreishi H., Ueda K., Arimura T., and Manabe O. J. Am. Chem. Soc. 109 (1987) 6371-6376
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  • 20
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    • For a similar study on 4-bromo-2,6-di-tert-butylcyclohexa-2,5-dienone, see:
    • For a similar study on 4-bromo-2,6-di-tert-butylcyclohexa-2,5-dienone, see:. Omura K. J. Org. Chem. 63 (1998) 10031-10034
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    • note
    • See Supplementary data for additional details.
  • 32
    • 66949179129 scopus 로고    scopus 로고
    • note
    • In addition to 3a and 4a, tripropoxy-p-tert-butylcalix[4]arene and tripropoxycalix[4]monoquinone were also isolated in 35% and 5% yield, respectively.
  • 33
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    • It is well known that 2,5-cyclohexadienone derivatives with two groups in position 4 undergo 1,2-migration of one of these groups (the dienone-phenol rearrangement) to afford phenolic compounds. For a review, see:
    • It is well known that 2,5-cyclohexadienone derivatives with two groups in position 4 undergo 1,2-migration of one of these groups (the dienone-phenol rearrangement) to afford phenolic compounds. For a review, see:. Miller B. Acc. Chem. Res. 8 (1975) 245-256
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    • Notwithstanding the special interest for the inherent chirality of meta-substituted calix[4]arenes, functionalizations at the meta-position are relatively uncommon. For some representative examples, see:
    • Notwithstanding the special interest for the inherent chirality of meta-substituted calix[4]arenes, functionalizations at the meta-position are relatively uncommon. For some representative examples, see:. Reddy P.A., and Gutsche C.D. J. Org. Chem. 58 (1993) 3245-3251
    • (1993) J. Org. Chem. , vol.58 , pp. 3245-3251
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  • 45
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    • For very interesting examples of non-chromatographic resolution of inherently chiral meta-substituted calixarenes, see:
    • For very interesting examples of non-chromatographic resolution of inherently chiral meta-substituted calixarenes, see:. Xu Z.-X., Zhang C., Zheng Q.-Y., Chen C.-F., and Huang Z.-T. Org. Lett. 9 (2007) 4447-4450
    • (2007) Org. Lett. , vol.9 , pp. 4447-4450
    • Xu, Z.-X.1    Zhang, C.2    Zheng, Q.-Y.3    Chen, C.-F.4    Huang, Z.-T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.