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Volumn 130, Issue 41, 2008, Pages 13524-13525

Enantioselective organocatalytic direct Michael addition of nitroalkanes to nitroalkenes promoted by a unique bifunctional DMAP-thiourea

Author keywords

[No Author keywords available]

Indexed keywords

2,2' DIAMINO 1,1'BINAPHTHYL; ALKENE DERIVATIVE; DIMETHYLAMINOPYRIDINE; LANTHANUM; NAPHTHYL GROUP; NITROALKANE; NITROALKENE; NITROGEN DERIVATIVE; PYRIDINE DERIVATIVE; TITANIUM; UNCLASSIFIED DRUG; ZINC;

EID: 53849128905     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja805390k     Document Type: Article
Times cited : (130)

References (25)
  • 5
    • 53849128714 scopus 로고    scopus 로고
    • See Supporting Information for a graphical survey of these catalysts and a complete list of citations
    • See Supporting Information for a graphical survey of these catalysts and a complete list of citations.
  • 10
    • 53849129759 scopus 로고    scopus 로고
    • For citations to the literature, see ref 8
    • For citations to the literature, see ref 8.
  • 18
    • 53849131868 scopus 로고    scopus 로고
    • 2O).
    • 2O).
  • 19
  • 25
    • 53849148090 scopus 로고    scopus 로고
    • One attempt with a β-alkyl substituted nitroalkene gave a much less selective outcome. Reaction of 1-nitro-1-pentene under the conditions in entry 1 of Table 2 (24 h) gave the Michael adduct in 66% yield with a dr of 58:42 and 42% ee for the major diastereomer.
    • One attempt with a β-alkyl substituted nitroalkene gave a much less selective outcome. Reaction of 1-nitro-1-pentene under the conditions in entry 1 of Table 2 (24 h) gave the Michael adduct in 66% yield with a dr of 58:42 and 42% ee for the major diastereomer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.