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Volumn , Issue 3, 2006, Pages 435-439

The Baylis-Hillman reaction with chiral α-amino aldehydes under racemization-free conditions

Author keywords

Aldehydes; Alkaloids; Amino aldehydes; Ring closure; Stereoselectivity

Indexed keywords

ALDEHYDE DERIVATIVE; ALPHA AMINO ALDEHYDE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33344473974     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nimb.2005.11.149     Document Type: Article
Times cited : (28)

References (52)
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  • 9
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    • For some recent examples concerning the utilization of Baylis-Hillman adduct as substrate for the synthesis of natural products and drugs, see: (a) Mateus, C. R.; Coelho, F. J. Braz. Chem. Soc. 2005, 16, 386-396; available free-of-charge at http://jbcs.sbq.org.br/online/2005/vol16_n3A/11-238-04.pdf.
    • (2005) J. Braz. Chem. Soc. , vol.16 , pp. 386-396
    • Mateus, C.R.1    Coelho, F.2
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    • For the anti relationship, an increment up to 1.9% was expected, see: (a) Schuch, C. M.; Pilli, R. A. Tetrahedron: Asymmetry 2000, 11, 153. For some examples describing the utilization of oxazolidines as a tool for the determination of relative stereochemistry, see:
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    • Schuch, C.M.1    Pilli, R.A.2
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    • For some examples in which chiral bicyclic lactam were used as advanced substrates for the synthesis of alkaloids see: (a) Muroni, D.; Saba, A.; Culeddu, N. Tetrahedron: Asymmetry 2004, 15, 2609.
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    • Muroni, D.1    Saba, A.2    Culeddu, N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.