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Volumn , Issue 3, 2011, Pages 578-583

4-aminothioureaprolinal dithioacetal as a catalyst for highly enantioselective michael additions of ketones and aldehydes to nitroolefins

Author keywords

Asymmetric catalysis; Enantioselectivity; Hydrogen bonds; Michael addition; Organocatalysis; Sulfur

Indexed keywords


EID: 78651322223     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001211     Document Type: Article
Times cited : (25)

References (78)
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    • For selected examples of using bulky groups to control stereochemistry, see
    • For selected examples of using bulky groups to control stereochemistry, see
  • 39
    • 78651340604 scopus 로고    scopus 로고
    • For selected examples of proline derivatives containing H-bonding moieties to control stereochemistry, see
    • For selected examples of proline derivatives containing H-bonding moieties to control stereochemistry, see
  • 53
    • 78651289491 scopus 로고    scopus 로고
    • For selected examples of using salts to control stereochemistry, see
    • For selected examples of using salts to control stereochemistry, see
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    • 33947605163 scopus 로고    scopus 로고
    • Vishnumaya.
    • Vishnumaya, V. K. Singh, Org. Lett. 2007, 9, 1117-1119.
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    • Singh, V.K.1
  • 70
    • 78651295459 scopus 로고    scopus 로고
    • To control stereochemistry by using H-bonding and bulky groups, see
    • To control stereochemistry by using H-bonding and bulky groups, see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.