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Volumn 13, Issue 15, 2011, Pages 4056-4059

A new synthesis of pyrrolidines by way of an enantioselective Mannich/diastereoselective hydroamination reaction sequence

Author keywords

[No Author keywords available]

Indexed keywords

HYDROGEN; PYRROLIDINE DERIVATIVE;

EID: 79961094527     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol201566u     Document Type: Article
Times cited : (22)

References (31)
  • 16
    • 0000365248 scopus 로고
    • For early studies on the generation of silyl ketene imines and their use in reactions with electrophiles, see
    • For early studies on the generation of silyl ketene imines and their use in reactions with electrophiles, see: Gornowicz, G. A.; West, R. J. Am. Chem. Soc. 1971, 93, 1714
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 1714
    • Gornowicz, G.A.1    West, R.2
  • 21
    • 13744263466 scopus 로고    scopus 로고
    • For two recent examples of the use of silyl ketene imines in asymmetric reactions, see
    • For two recent examples of the use of silyl ketene imines in asymmetric reactions, see: Mermerian, A. H.; Fu, G. C. Angew. Chem., Int. Ed. 2005, 44, 949
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 949
    • Mermerian, A.H.1    Fu, G.C.2
  • 23
    • 24044441607 scopus 로고    scopus 로고
    • For other examples of Mannich-type reactions with acylhydrazones, see
    • For other examples of Mannich-type reactions with acylhydrazones, see: Sugiura, M.; Kobayashi, S. Angew. Chem., Int. Ed. 2005, 44, 5176
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 5176
    • Sugiura, M.1    Kobayashi, S.2
  • 24
    • 18844456337 scopus 로고    scopus 로고
    • The effective use of disubstituted enolates or enolate equivalents in enantioselective Mannich reactions for the generation of all-carbon quaternary stereocenters is extremely rare (and, with hydrazones as the electrophile, nonexistent). See
    • The effective use of disubstituted enolates or enolate equivalents in enantioselective Mannich reactions for the generation of all-carbon quaternary stereocenters is extremely rare (and, with hydrazones as the electrophile, nonexistent). See: Poulsen, T. B.; Alemparte, C.; Saaby, S.; Bella, M.; Jørgensen, K. A. Angew. Chem., Int. Ed. 2005, 44, 2896
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 2896
    • Poulsen, T.B.1    Alemparte, C.2    Saaby, S.3    Bella, M.4    Jørgensen, K.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.