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Volumn 14, Issue 8, 2012, Pages 2150-2153

Asymmetric total synthesis and absolute stereochemistry of the neuroactive marine macrolide palmyrolide A

Author keywords

[No Author keywords available]

Indexed keywords

COPPER; CUPROUS IODIDE; IODIDE; MACROLIDE; PALMYROLIDE A;

EID: 84860117782     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol300673m     Document Type: Article
Times cited : (39)

References (49)
  • 3
    • 84860174594 scopus 로고    scopus 로고
    • This method was successfully applied to the structure elucidation of the (-)-apratoxin A macrolide. See ref 3a.
    • This method was successfully applied to the structure elucidation of the (-)-apratoxin A macrolide. See ref 3a.
  • 17
    • 84860187985 scopus 로고    scopus 로고
    • Personal communication, 2011
    • Personal communication, 2011.
  • 40
    • 0034622871 scopus 로고    scopus 로고
    • For a review article documenting the reactivity of cyclic sulfates, see: Byun, H.-S.; He, L.; Bittman, R. Tetrahedron 2000, 56, 7051-7091
    • (2000) Tetrahedron , vol.56 , pp. 7051-7091
    • Byun, H.-S.1    He, L.2    Bittman, R.3
  • 46
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.