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Volumn 19, Issue 4, 2008, Pages 467-475

Highly diastereoselective approach to novel tetrahydrofuran-fused indolizidinols: a one-step formation of three contiguous stereocenters

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE; FURAN DERIVATIVE; INDOLIZINE DERIVATIVE; TETRAHYDROFURAN;

EID: 39949083371     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.01.013     Document Type: Article
Times cited : (14)

References (53)
  • 6
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    • and other references cited therein
    • Michael J.P. Nat. Prod. Rep. 22 (2005) 603 and other references cited therein
    • (2005) Nat. Prod. Rep. , vol.22 , pp. 603
    • Michael, J.P.1
  • 26
    • 33747405857 scopus 로고    scopus 로고
    • For another recent attractive route to enantiopure carbon and hetero-7-substituted swainsonine analogues, see:
    • For another recent attractive route to enantiopure carbon and hetero-7-substituted swainsonine analogues, see:. Tinarelli A., and Paolucci C. J. Org. Chem. 71 (2006) 6630
    • (2006) J. Org. Chem. , vol.71 , pp. 6630
    • Tinarelli, A.1    Paolucci, C.2
  • 32
    • 0023333694 scopus 로고
    • For a few known other strategies toward indolizidines using (S)-glutamic acid, see:
    • For a few known other strategies toward indolizidines using (S)-glutamic acid, see:. Ikota N., and Hanaki A. Chem. Pharm. Bull. 35 (1987) 2140
    • (1987) Chem. Pharm. Bull. , vol.35 , pp. 2140
    • Ikota, N.1    Hanaki, A.2
  • 46
    • 39949084910 scopus 로고    scopus 로고
    • note
    • This diagnostic is limited to the experiments catalyzed with Ra-Ni.
  • 47
    • 39949084178 scopus 로고    scopus 로고
    • note
    • The following results were obtained: iPrOH 4/5: 57/43, THF 4/5: 49/51, AcOEt 4/5: 52/48.
  • 48
    • 0034625892 scopus 로고    scopus 로고
    • For selectivity-enhancing effect of an ADmix additive in the catalytic hydrogenation of heteroaromatic cycles, see:
    • For selectivity-enhancing effect of an ADmix additive in the catalytic hydrogenation of heteroaromatic cycles, see:. Kuwano R., Sato K., Kurokawa T., Karube D., and Ito Y. J. Am. Chem. Soc. 122 (2000) 7614
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 7614
    • Kuwano, R.1    Sato, K.2    Kurokawa, T.3    Karube, D.4    Ito, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.