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Volumn 71, Issue 26, 2006, Pages 9891-9894

New aniline-containing amino alcohols from trans-(r,r)-2-(2-nitrophenyl)-3- phenyloxirane as useful intermediates for the synthesis of chiral ligands, bases, and benzoxazine nucleus

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ALCOHOLS; ANILINE; CHIRAL LIGANDS; OPTICAL PURITY;

EID: 33845932909     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0617969     Document Type: Article
Times cited : (13)

References (34)
  • 7
    • 4243863543 scopus 로고
    • US Pat. 4030906, 79678e
    • (a) Kobzina, J. W. US Pat. 4030906, 1977; Chem. Abstr. 1977, 87, 79678e.
    • (1977) Chem. Abstr , vol.87
    • Kobzina, J.W.1
  • 8
    • 33845938837 scopus 로고    scopus 로고
    • Imperial Chemistry Industries Ltd. Jpn. Pat. 8047665, 1980: Chem. Abstr. 1980, 93, 204681c.
    • (b) Imperial Chemistry Industries Ltd. Jpn. Pat. 8047665, 1980: Chem. Abstr. 1980, 93, 204681c.
  • 9
    • 33845914950 scopus 로고    scopus 로고
    • Boyle, F. T.; Taylor, M. A. Span. Pat. 1980, 484472; Chem. Abstr. 1981, 94, 156956t.
    • Boyle, F. T.; Taylor, M. A. Span. Pat. 1980, 484472; Chem. Abstr. 1981, 94, 156956t.
  • 18
    • 0000758818 scopus 로고    scopus 로고
    • For the synthesis of 6 from (R,R,R)-oxathiane, see: Vedejs, E.; Engler, D. A.; Mullins, M. J. J. Org. Chem. 1977, 42, 3109-3113.
    • For the synthesis of 6 from (R,R,R)-oxathiane, see: Vedejs, E.; Engler, D. A.; Mullins, M. J. J. Org. Chem. 1977, 42, 3109-3113.
  • 19
    • 33845949273 scopus 로고    scopus 로고
    • For the synthesis of (R,R,R)-oxathiane, see: Eliel, E. L.; Lynch, J. E.; Kume, F.; Frye, S. V. Org. Synth. 1987, 65, 215-221.
    • For the synthesis of (R,R,R)-oxathiane, see: Eliel, E. L.; Lynch, J. E.; Kume, F.; Frye, S. V. Org. Synth. 1987, 65, 215-221.
  • 32
    • 33845950073 scopus 로고    scopus 로고
    • In a typical procedure, a MgClO4/H2O 1:10 molar ratio was used
    • 2O 1:10 molar ratio was used.
  • 33
    • 33845916267 scopus 로고    scopus 로고
    • When the reaction was performed on amino alcohols 6 and 7, an approximately equimolar mixture of the different products 11, 12, 17, 18, and N-Boc tert-butyl ethers was formed.
    • When the reaction was performed on amino alcohols 6 and 7, an approximately equimolar mixture of the different products 11, 12, 17, 18, and N-Boc tert-butyl ethers was formed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.