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Synlett
Volumn , Issue 4, 2000, Pages 442-454
Nucleophilic additions to chiral nitrones: New approaches to nitrogenated compounds
Author keywords

Amino acids; Carbohydrates; Hydroxylamines; Nitrones; Nucleosides
Indexed keywords

AMINO ACID; CARBOHYDRATE; HYDROXYLAMINE; NITRONE DERIVATIVE; NUCLEOSIDE;
EID: 0034112410     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (164)
References (111)
  • 1
    • 0342569636 scopus 로고    scopus 로고
    • Formation of C-C bonds by addition to imino groups
    • Thieme: Stuttgart and references cited therein
    • Formation of C-C bonds by Addition to Imino Groups (several authors) In Stereoselective Synthesis, Houben-Weyl; Helmchen, G.; Hoffmann, R.W.; Mulzer, J.; Schaumann, E., Eds.; Thieme: Stuttgart 1996; Vol. 3, p 1833 and references cited therein.
    • (1996) Stereoselective Synthesis , vol.3 , pp. 1833
    • Houben-Weyl1    Helmchen, G.2    Hoffmann, R.W.3    Mulzer, J.4    Schaumann, E.5
  • 5
  • 13
    • 0001357078 scopus 로고    scopus 로고
    • Attanasi, O. A.; Spinelli, D., Eds., Italian Society of Chemistry: Rome
    • (g) Chiacchio, U.; Rescifina, A.; Romeo, G. In Targets in Heterocyclic Systems, Attanasi, O. A.; Spinelli, D., Eds., Italian Society of Chemistry: Rome 1997, Vol. 1, p 225.
    • (1997) Targets in Heterocyclic Systems , vol.1 , pp. 225
    • Chiacchio, U.1    Rescifina, A.2    Romeo, G.3
  • 21
    • 0343518308 scopus 로고
    • Most of work described in this report has been taken from five Ph.D. thesis presented at the University of Zaragoza: (a) Franco, S. 1994.
    • (1994)
    • Franco, S.1
  • 23
  • 34
  • 44
    • 84985553225 scopus 로고
    • In this Account we use the syn/anti nomenclature according to Masamune convention (See: Masamune, S.; Ali, S.A.; Snitman, D.L.; Garvey, D.S. Angew. Chem. Int. Ed. Engl. 1980, 19, 557 and Masamune, S.; Kaiho, T.; Garvey, D.S. J. Am. Chem. Soc. 1982, 104, 5521). Diastereoselectivities are indicated as diastereomeric ratios in the form of ds, as recommended for stereoselective reactions in which two isomers can be obtained. In addition the Re/Si nomenclature is used for the description of the topicity of the approach of reagent (nucleophile) and substrate (nitrone). For an excellent and comprehensive discussion on the terminology used in stereochemistry see: Helmchen, G. In Stereoselective Synthesis, Houben-Weyl; Helmchen, G.; Hoffmann, R.W.; Mulzer, J.; Schaumann, E., Eds.; Thieme: Stuttgart 1996; Vol. 1, p. 1.
    • (1980) Angew. Chem. Int. Ed. Engl. , vol.19 , pp. 557
    • Masamune, S.1    Ali, S.A.2    Snitman, D.L.3    Garvey, D.S.4
  • 45
    • 33845555760 scopus 로고
    • In this Account we use the syn/anti nomenclature according to Masamune convention (See: Masamune, S.; Ali, S.A.; Snitman, D.L.; Garvey, D.S. Angew. Chem. Int. Ed. Engl. 1980, 19, 557 and Masamune, S.; Kaiho, T.; Garvey, D.S. J. Am. Chem. Soc. 1982, 104, 5521). Diastereoselectivities are indicated as diastereomeric ratios in the form of ds, as recommended for stereoselective reactions in which two isomers can be obtained. In addition the Re/Si nomenclature is used for the description of the topicity of the approach of reagent (nucleophile) and substrate (nitrone). For an excellent and comprehensive discussion on the terminology used in stereochemistry see: Helmchen, G. In Stereoselective Synthesis, Houben-Weyl; Helmchen, G.; Hoffmann, R.W.; Mulzer, J.; Schaumann, E., Eds.; Thieme: Stuttgart 1996; Vol. 1, p. 1.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5521
    • Masamune, S.1    Kaiho, T.2    Garvey, D.S.3
  • 46
    • 0004005458 scopus 로고    scopus 로고
    • Houben-Weyl; Helmchen, G.; Hoffmann, R.W.; Mulzer, J.; Schaumann, E., Eds.; Thieme: Stuttgart
    • In this Account we use the syn/anti nomenclature according to Masamune convention (See: Masamune, S.; Ali, S.A.; Snitman, D.L.; Garvey, D.S. Angew. Chem. Int. Ed. Engl. 1980, 19, 557 and Masamune, S.; Kaiho, T.; Garvey, D.S. J. Am. Chem. Soc. 1982, 104, 5521). Diastereoselectivities are indicated as diastereomeric ratios in the form of ds, as recommended for stereoselective reactions in which two isomers can be obtained. In addition the Re/Si nomenclature is used for the description of the topicity of the approach of reagent (nucleophile) and substrate (nitrone). For an excellent and comprehensive discussion on the terminology used in stereochemistry see: Helmchen, G. In Stereoselective Synthesis, Houben-Weyl; Helmchen, G.; Hoffmann, R.W.; Mulzer, J.; Schaumann, E., Eds.; Thieme: Stuttgart 1996; Vol. 1, p. 1.
    • (1996) Stereoselective Synthesis , vol.1 , pp. 1
    • Helmchen, G.1
  • 54
    • 0343954157 scopus 로고    scopus 로고
    • unpublished theoretical calculations
    • Merino, P.; Tejero, T. unpublished theoretical calculations.
    • Merino, P.1    Tejero, T.2

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.