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Volumn 66, Issue 39, 2010, Pages 7707-7719

Enantioselective synthesis of butadien-2-ylcarbinols via (silylmethyl)allenic alcohols from chromium-catalyzed additions to aldehydes utilizing chiral carbazole ligands

Author keywords

Asymmetric catalysis; Carbazole ligands; Chromium; Dienes; Regioselectivity

Indexed keywords

ALCOHOL DERIVATIVE; BUTADIEN 2 YLCARBINOL DERIVATIVE; CARBAZOLE DERIVATIVE; CHROMIUM; METHANOL DERIVATIVE; SUCCINIMIDE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77956382088     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.07.065     Document Type: Article
Times cited : (19)

References (59)
  • 46
    • 77956373784 scopus 로고    scopus 로고
    • When a bulkier silyl group such as DMPS was used as a substituent on the propargyl bromide, a decrease in the product yield and %ee was observed
    • When a bulkier silyl group such as DMPS was used as a substituent on the propargyl bromide, a decrease in the product yield and %ee was observed.
  • 51
    • 77956360233 scopus 로고    scopus 로고
    • Our attempts to synthesize 1,3,6,8-tetraiodo-9H-carbazole were unsuccessful
    • Our attempts to synthesize 1,3,6,8-tetraiodo-9H-carbazole were unsuccessful.
  • 54
    • 77956378806 scopus 로고    scopus 로고
    • Chiral amino alcohol 4f was obtained in semipure form as a yellow oil in 55% yield by LAH reduction of (2S,3R)-2-amino-3-methoxybutanoic acid and used without further purification
    • Chiral amino alcohol 4f was obtained in semipure form as a yellow oil in 55% yield by LAH reduction of (2S,3R)-2-amino-3-methoxybutanoic acid and used without further purification.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.