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Volumn 70, Issue 11, 2005, Pages 4470-4473

Fluorous mixture synthesis of fused-tricyclic hydantoins. Use of a redundant tagging strategy on fluorinated substrates

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MIXTURES; SUBSTRATES; SYNTHESIS (CHEMICAL);

EID: 19544368155     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0502596     Document Type: Article
Times cited : (26)

References (25)
  • 5
    • 10844297488 scopus 로고    scopus 로고
    • (e) Short review: Zhang, W. Arkivoc 2004, 101-109.
    • (2004) Arkivoc , pp. 101-109
    • Zhang, W.1
  • 7
    • 3943111078 scopus 로고    scopus 로고
    • Gladysz, J. A., Curran, D. P., Horvath, I., Eds.; Wiley-VCH: Weinheim
    • (b) Curran, D. P. In Handbook of Fluorous Chemistry; Gladysz, J. A., Curran, D. P., Horvath, I., Eds.; Wiley-VCH: Weinheim, 2004; pp 101-128.
    • (2004) Handbook of Fluorous Chemistry , pp. 101-128
    • Curran, D.P.1
  • 10
    • 4544353451 scopus 로고    scopus 로고
    • (c) Ojima, I. ChemBioChem 2004, 5, 628-635. This issue of ChemBioChem also contains other articles and reviews regarding fluorine in the life sciences.
    • (2004) ChemBioChem , vol.5 , pp. 628-635
    • Ojima, I.1
  • 12
    • 13544273419 scopus 로고    scopus 로고
    • Manku, S.; Curran, D. P. J. Comb. Chem. 2005, 7, 63-68. In this work, secondary propargyl esters [RCOOCH(Me)C≡CTMS] were studied.
    • (2005) J. Comb. Chem. , vol.7 , pp. 63-68
    • Manku, S.1    Curran, D.P.2
  • 14
    • 19544372121 scopus 로고    scopus 로고
    • (b) The fluorous reagents and columns were purchased from Fluorous Technologies, Inc. (www.fluorous.com).
  • 15
    • 19544383258 scopus 로고    scopus 로고
    • note
    • (c) DPC holds an equity interest in this company.
  • 16
    • 0141854273 scopus 로고    scopus 로고
    • For another example of fluorous synthesis of hydantoins, see: Zhang, W.; Lu, Y. Org. Lett. 2003, 5, 2555-2558.
    • (2003) Org. Lett. , vol.5 , pp. 2555-2558
    • Zhang, W.1    Lu, Y.2
  • 17
    • 2942545969 scopus 로고    scopus 로고
    • For a review on the use of fluorous reagents for the synthesis of heterocycles, see: Zhang, W. Chem. Rev. 2004, 104, 2531-2556.
    • (2004) Chem. Rev. , vol.104 , pp. 2531-2556
    • Zhang, W.1
  • 18
    • 3142712364 scopus 로고    scopus 로고
    • For the use of Rh(I) catalysts on alkynyl allenes, see: (a) Brummond, K. M.; Mitasev, B. Org. Lett. 2004, 6, 2245-2248.
    • (2004) Org. Lett. , vol.6 , pp. 2245-2248
    • Brummond, K.M.1    Mitasev, B.2
  • 22
    • 19544373652 scopus 로고    scopus 로고
    • note
    • Trimethylsilylpropargyl alcohol, which was used in the initial tag assignments, failed to undergo the ester-enolate Claisen rearrangement cleanly.
  • 24
    • 19544368499 scopus 로고    scopus 로고
    • note
    • 1 = Me) gave a 4/1 mixture of 10-syn/10-anti with little or no 11. Full details can be found in Supporting Information.
  • 25
    • 0038260112 scopus 로고    scopus 로고
    • Zhang, W. Org. Lett. 2003, 5, 1011-1013.
    • (2003) Org. Lett. , vol.5 , pp. 1011-1013
    • Zhang, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.