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Volumn 77, Issue 14, 2012, Pages 6271-6289

Evolution of a protecting-group-free total synthesis: Studies en route to the neuroactive marine macrolide (-)-palmyrolide A

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE STEREOCHEMISTRY; DEGRADATION PRODUCTS; DIASTEREOMERS; EN-ROUTE; MACROLIDES; TOTAL SYNTHESIS;

EID: 84864056903     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo301121f     Document Type: Article
Times cited : (37)

References (92)
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    • For review on the determination of relative configuration by NMR and computational methods, see
    • For review on the determination of relative configuration by NMR and computational methods, see: Bifulco, G.; Dambruoso, P.; Gomez-Paloma, L.; Riccio, R. Chem. Rev. 2007, 107, 3744-3779
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  • 19
    • 0030912795 scopus 로고    scopus 로고
    • For a review article showcasing several examples, see
    • For a review article showcasing several examples, see: Gournelis, D. C.; Laskaris, G. G.; Verpoorte, R. Nat. Prod. Rep. 1997, 14, 75-82
    • (1997) Nat. Prod. Rep. , vol.14 , pp. 75-82
    • Gournelis, D.C.1    Laskaris, G.G.2    Verpoorte, R.3
  • 53
    • 84860724488 scopus 로고    scopus 로고
    • For the latest modification that uses pseudoephenamine, see
    • For the latest modification that uses pseudoephenamine, see: Morales, M. R.; Mellem, K. T.; Myers, A. G. Angew. Chem., Int. Ed. 2012, 51, 4568-4571
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 4568-4571
    • Morales, M.R.1    Mellem, K.T.2    Myers, A.G.3
  • 60
    • 77956640932 scopus 로고    scopus 로고
    • A possible explanation for our inability to form the vinyl triflate may be competing amide activation under these conditions. For a lead reference, see
    • A possible explanation for our inability to form the vinyl triflate may be competing amide activation under these conditions. For a lead reference, see: Pelletier, G.; Bechara, W. S.; Charette, A. B. J. Am. Chem. Soc. 2010, 132, 12817-12819
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 12817-12819
    • Pelletier, G.1    Bechara, W.S.2    Charette, A.B.3
  • 71
    • 0035794963 scopus 로고    scopus 로고
    • Our initial attempts using acrylamide and the Grubbs II precatalyst gave good, but somewhat inferior, results compared to acryloyl chloride (36% vs 58%, respectively). For a lead reference, see
    • Our initial attempts using acrylamide and the Grubbs II precatalyst gave good, but somewhat inferior, results compared to acryloyl chloride (36% vs 58%, respectively). For a lead reference, see: Choi, T.-L.; Chatterjee, A. K.; Grubbs, R. H. Angew. Chem., Int. Ed. 2001, 40, 1277-1279
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 1277-1279
    • Choi, T.-L.1    Chatterjee, A.K.2    Grubbs, R.H.3
  • 75
    • 33748617140 scopus 로고    scopus 로고
    • Alcohol 7 can also be prepared in one synthetic step from 3-butyn-1-ol. See: Huang, Z.; Negishi, E.-i. Org. Lett. 2006, 8, 3675-3678
    • (2006) Org. Lett. , vol.8 , pp. 3675-3678
    • Huang, Z.1    Negishi, E.-I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.