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Volumn 127, Issue 19, 2005, Pages 7014-7024

Development of aliphatic alcohols as nucleophiles for palladium-catalyzed DYKAT reactions: Total synthesis of (+)-hippospongic acid A

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; ALKYLATION; CATALYSIS; COMPLEXATION; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 18744386668     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja050340q     Document Type: Article
Times cited : (123)

References (63)
  • 22
    • 18744417153 scopus 로고    scopus 로고
    • note
    • Matched implies that the reaction pathway is favored by the given enantiomer of chiral ligand.
  • 23
    • 18744370654 scopus 로고    scopus 로고
    • note
    • Full experimental details for all intermediates and products are reported in the Supporting Information.
  • 25
    • 18744390977 scopus 로고    scopus 로고
    • note
    • L-3 has been successfully used to effect alkylations on bulky or otherwise sterically encumbered substrates. For an example relating to DYKAT reactions, see ref 11.
  • 55
    • 85026854437 scopus 로고    scopus 로고
    • Vinyl bromide 56 is made by simple Markovnikov addition of dry hydrogen bromide gas across propargyl alcohol, followed by silyl protection: Marshall, J. A.; Sehon, C. A. Org. Synth. 1999, 76, 263.
    • (1999) Org. Synth. , vol.76 , pp. 263
    • Marshall, J.A.1    Sehon, C.A.2
  • 63
    • 18744379056 scopus 로고    scopus 로고
    • note
    • Our spectral data matched those previously reported in refs 25 and 26.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.