메뉴 건너뛰기




Volumn 16, Issue 47, 2010, Pages 14074-14082

Short diastereoselective synthesis of the C1-C13 (AB Spiroacetal) and C17-C28 fragments (CD spiroacetal) of spongistatin 1 and 2 through double chain-elongation reactions

Author keywords

double chain elongation; enantioselectivity; Hosomi Sakurai reaction; spiro compounds; spongistatin

Indexed keywords

ALLYLATIONS; ALLYLSILANES; DIASTEREOSELECTIVE SYNTHESIS; DOUBLE CHAIN; LINEAR SEQUENCE; POLYKETIDES; RING SYSTEMS; SAKURAI; SPIRO COMPOUNDS; SPONGISTATIN; SPONGISTATIN 1; SYNTHETIC SEQUENCE;

EID: 78650266449     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002204     Document Type: Article
Times cited : (6)

References (160)
  • 32
  • 50
  • 79
    • 24644506223 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 5433-5438
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 5433-5438
  • 132
    • 0032890482 scopus 로고    scopus 로고
    • For a convergent synthesis of a polyol chain by using this reagent
    • For a convergent synthesis of a polyol chain by using this reagent, see:, S. D. Rychnovsky, O. Fryszman, U. R. Khire, Tetrahedron Lett. 1999, 40, 41-44.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 41-44
    • Rychnovsky, S.D.1    Fryszman, O.2    Khire, U.R.3
  • 135
    • 78650286024 scopus 로고    scopus 로고
    • When (2-((trimethylsilyl)methyl)allyl)trimethylsilane was used a 1-methyl-1-alkylethene (loss of TMS) was obtained
    • When (2-((trimethylsilyl)methyl)allyl)trimethylsilane was used a 1-methyl-1-alkylethene (loss of TMS) was obtained.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.