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Volumn , Issue 13, 2007, Pages 2114-2120

Highly stereoselective synthesis of stereochemically defined polyhydroxylated propargylamines by alkynylation of N-benzylimines derived from (R)-glyceraldehyde

Author keywords

Amino alcohols; Asymmetric synthesis; Diastereoselectivity; Nucleophilic addition; Schiff bases

Indexed keywords


EID: 34250686268     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200601011     Document Type: Article
Times cited : (17)

References (66)
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    • Recent examples of diastereoselective additions: a R. B. Lettan II, K. A. Scheidt, Org. Lett. 2005, 7, 3227-3230;
    • Recent examples of diastereoselective additions: a) R. B. Lettan II, K. A. Scheidt, Org. Lett. 2005, 7, 3227-3230;
  • 22
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    • Recent examples of enantioselective additions: a F. Colombo, M. Benaglia, S. Orlandi, F. Usuelli, G. Celentano, J. Org. Chem. 2006, 71, 2064-2070;
    • Recent examples of enantioselective additions: a) F. Colombo, M. Benaglia, S. Orlandi, F. Usuelli, G. Celentano, J. Org. Chem. 2006, 71, 2064-2070;
  • 35
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    • b) R. Bloch, Chem. Rev. 1998, 98, 1407-1438;
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    • For some recent examples, see: a
    • For some recent examples, see: a) M. Achmatowicz, L. S. Hegedus, J. Org. Chem. 2004, 69, 2229-2234;
    • (2004) J. Org. Chem , vol.69 , pp. 2229-2234
    • Achmatowicz, M.1    Hegedus, L.S.2
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    • 0010771837 scopus 로고    scopus 로고
    • For a review of chelation and non-chelation control in addition reactions of chiral α-alkoxy carbonyl compounds, see: M. T. Reetz, Angew. Chem. Int. Ed. Engl. 1984, 23, 556-569
    • For a review of chelation and non-chelation control in addition reactions of chiral α-alkoxy carbonyl compounds, see: M. T. Reetz, Angew. Chem. Int. Ed. Engl. 1984, 23, 556-569.
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    • For a review of multiple stereoselectivity, see
    • For a review of multiple stereoselectivity, see: O. J. Kolodiazhnyi, Tetrahedron 2003, 59, 5953-6018.
    • (2003) Tetrahedron , vol.59 , pp. 5953-6018
    • Kolodiazhnyi, O.J.1
  • 64
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    • 3NHAcO, pH4.0; room temp, for (S)-glutamic acid 5.1 min; room temp, for (R)-glutamic acid 7.4 min.
    • 3NHAcO, pH4.0; room temp, for (S)-glutamic acid 5.1 min; room temp, for (R)-glutamic acid 7.4 min.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.