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Volumn , Issue 23, 2006, Pages 4087-4091

An enantio- and diastereoselective synthesis of fluorinated β-aminoalkyloxepine derivatives through Mannich and ring-closing metathesis reactions

Author keywords

Amino alcohols; Fluorine; Mannich reaction; Metathesis; Organocatalysis; Oxepines

Indexed keywords

DERIVATIVES; ETHERS; FLUORINE; REDUCTION; STEREOCHEMISTRY; SUBSTRATES; SYNTHESIS (CHEMICAL);

EID: 33845608013     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-950345     Document Type: Article
Times cited : (17)

References (48)
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    • Organo-fluorine compounds
    • Georg Thieme Verlag: Stuttgart
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    • 0034721440 scopus 로고    scopus 로고
    • For representative examples of organocatalyzed Mannich reactions, see: (a) List, B. J. Am. Chem. Soc. 2000, 122, 9336.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9336
    • List, B.1
  • 34
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    • Berkessel, A.; Gröger, H., Eds.; Wiley-VCH: Weinheim
    • (a) Asymmetric Organocatalysis; Berkessel, A.; Gröger, H., Eds.; Wiley-VCH: Weinheim, 2005.
    • (2005) Asymmetric Organocatalysis
  • 47
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    • note
    • In the case of γ-amino alcohol 2c, however, the yield in the O-allylation reaction was substantially lower because of competitive side reactions. As the O-allylation product turned out to be very difficult to purify, we decided not to continue with this substrate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.