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Volumn 5, Issue 12, 2010, Pages 2459-2462

Rapid assembly of resorcylic acid lactone frameworks through sequential palladium-catalyzed coupling reactions

Author keywords

antitumor agents; carbonylation; macrocycles; metathesis; palladium

Indexed keywords

ANTI-TUMOR AGENTS; CATALYZED COUPLING; EFFICIENT SYNTHESIS; MACROCYCLES; METATHESIS; RING-CLOSING METATHESIS REACTIONS;

EID: 78650112447     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201000534     Document Type: Article
Times cited : (28)

References (50)
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    • It has been reported in Ref. [2] that the Mitsunobu esterification requires the ortho-phenol unprotected to get the best yield. On the other hand, the RCM reaction usually worked best with the ortho-phenol protected
    • It has been reported in Ref. [2] that the Mitsunobu esterification requires the ortho-phenol unprotected to get the best yield. On the other hand, the RCM reaction usually worked best with the ortho-phenol protected.
  • 10
    • 0242636003 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 5230-5234.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5230-5234
  • 18
    • 33749026617 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 6086-6101.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 6086-6101
  • 26
    • 78650122530 scopus 로고    scopus 로고
    • See Supporting Information for detailed preparation of the aromatic scaffolds 4 and 5
    • See Supporting Information for detailed preparation of the aromatic scaffolds 4 and 5.
  • 27
    • 78650141304 scopus 로고    scopus 로고
    • See Supporting Information for detailed preparation of the 7 c - 7 g
    • See Supporting Information for detailed preparation of the 7 c-7 g.
  • 40
  • 41
    • 0038373087 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 2826-2830.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 2826-2830
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    • 78650105776 scopus 로고    scopus 로고
    • the RCM reaction of alkene 18 with the Grubbs II catalyst, a substantial amount of the undesired 6-membered ring product was generated
    • In the RCM reaction of alkene 18 with the Grubbs II catalyst, a substantial amount of the undesired 6-membered ring product was generated.
  • 46
    • 78650131787 scopus 로고    scopus 로고
    • Terminal trisubstituted alkene 7 g was used to suppress the undesired 6-membered ring formation under the existence of the Grubbs II catalyst. 7 g can be prepared from citronellal in short steps
    • Terminal trisubstituted alkene 7 g was used to suppress the undesired 6-membered ring formation under the existence of the Grubbs II catalyst. 7 g can be prepared from citronellal in short steps.
  • 48
    • 34548779745 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 6899-6902.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 6899-6902
  • 50
    • 78650136200 scopus 로고    scopus 로고
    • 50=17.4 μ M)
    • 50=17.4 μ M).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.