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Volumn 12, Issue 14, 2010, Pages 3234-3237

Facile approach to optically active α-Alkylidene-β-amino esters by thermal overman rearrangement

Author keywords

[No Author keywords available]

Indexed keywords


EID: 77954547147     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1011746     Document Type: Article
Times cited : (19)

References (51)
  • 8
    • 77954544035 scopus 로고    scopus 로고
    • For catalytic enantioselective rearrangement of imidate, see
    • For catalytic enantioselective rearrangement of imidate, see
  • 19
    • 77954546950 scopus 로고    scopus 로고
    • For a recent reports on cationic oxazaborolidinium, see
    • For a recent reports on cationic oxazaborolidinium, see
  • 26
    • 77954561677 scopus 로고    scopus 로고
    • For a review on (Z)- β-halo MBH ester synthesis, see
    • For a review on (Z)- β-halo MBH ester synthesis, see
  • 32
    • 77954560081 scopus 로고    scopus 로고
    • For other routes to β-branched MBH products, see
    • For other routes to β-branched MBH products, see
  • 40
    • 77954558498 scopus 로고    scopus 로고
    • For other methods to α-alkylidene-β-amino esters, see
    • For other methods to α-alkylidene-β-amino esters, see
  • 46
    • 77954543930 scopus 로고    scopus 로고
    • The Overman rearrangement of (E)-stereoisomer of 7a provided 8a in lower E/Z -ratio (∼2.5/1) and 73% yield
    • The Overman rearrangement of (E)-stereoisomer of 7a provided 8a in lower E / Z -ratio (∼2.5/1) and 73% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.