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Volumn 50, Issue 23, 2009, Pages 2797-2800

Studies toward the total synthesis of the hirsutellones

Author keywords

[No Author keywords available]

Indexed keywords

HIRSUTELLONE A; HIRSUTELLONE B; HIRSUTELLONE C; HIRSUTELLONE D; HIRSUTELLONE E; KETENE DERIVATIVE; NATURAL PRODUCT; UNCLASSIFIED DRUG;

EID: 64549159707     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.03.158     Document Type: Article
Times cited : (30)

References (32)
  • 10
    • 60849120481 scopus 로고    scopus 로고
    • When this manuscript is in preparation, an elegant synthesis of the decahydrofluorene core of the hirsutellones is reported:
    • When this manuscript is in preparation, an elegant synthesis of the decahydrofluorene core of the hirsutellones is reported:. Tilley S.D., Reber K.P., and Sorensen E.J. Org. Lett. 11 (2009) 701-703
    • (2009) Org. Lett. , vol.11 , pp. 701-703
    • Tilley, S.D.1    Reber, K.P.2    Sorensen, E.J.3
  • 14
    • 64549132320 scopus 로고    scopus 로고
    • note
    • A seven-step sequence was followed to prepare 12:{A figure is presented}.
  • 15
    • 64549101803 scopus 로고    scopus 로고
    • A routine synthetic sequence was followed to afford 17: {A figure is presented}.
    • A routine synthetic sequence was followed to afford 17: {A figure is presented}.
  • 16
    • 0037956005 scopus 로고    scopus 로고
    • For selective deprotection of phenolic TBS ether, see:
    • For selective deprotection of phenolic TBS ether, see:. Ankala S.V., and Fenteany G. Synlett (2003) 825-828
    • (2003) Synlett , pp. 825-828
    • Ankala, S.V.1    Fenteany, G.2
  • 25
    • 3242683644 scopus 로고    scopus 로고
    • For an example, see:
    • For an example, see:. Cook G.R., and Sun L. Org. Lett. 6 (2004) 2481-2484
    • (2004) Org. Lett. , vol.6 , pp. 2481-2484
    • Cook, G.R.1    Sun, L.2
  • 27
    • 64549116541 scopus 로고    scopus 로고
    • note
    • + 592.3434, found 592.3445.
  • 30
    • 0023043811 scopus 로고
    • Houk's modeling on conformational preferenes of allylic groups in transition structures does not account for our result, see:
    • Houk's modeling on conformational preferenes of allylic groups in transition structures does not account for our result, see:. Houk K.N., Paddon-Row M.N., Rondan N.G., Wu Y., Brown F.K., Spellmeyer D.C., Metz J.T., Li Y., and Loncharich R.J. Science 231 (1986) 1108-1117
    • (1986) Science , vol.231 , pp. 1108-1117
    • Houk, K.N.1    Paddon-Row, M.N.2    Rondan, N.G.3    Wu, Y.4    Brown, F.K.5    Spellmeyer, D.C.6    Metz, J.T.7    Li, Y.8    Loncharich, R.J.9
  • 31
    • 12944325309 scopus 로고    scopus 로고
    • For the examples of similar IMDA reactions consistent with Houk's modeling, see:
    • For the examples of similar IMDA reactions consistent with Houk's modeling, see:. Jarosz S., Boryczko B., Cmoch P., Gomez A.M., and Lopez C. Tetrahedron: Asymmetry 16 (2005) 513-518
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 513-518
    • Jarosz, S.1    Boryczko, B.2    Cmoch, P.3    Gomez, A.M.4    Lopez, C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.