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Volumn 352, Issue 10, 2010, Pages 1657-1661

Chemo- And stereodivergent preparation of terminal epoxides and bromohydrins through One-Pot biocatalysed reactions: Access to enantiopure Five- and Six-Membered N-Heterocycles

Author keywords

Alcohol dehydrogenases; Bromohydrins; Epoxides; Medium engineering; One pot reaction; Prolinol

Indexed keywords


EID: 77954777151     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201000353     Document Type: Article
Times cited : (21)

References (53)
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    • These substrates can easily be obtained starting from the corresponding ketones or alkenes. See, for instance: a
    • These substrates can easily be obtained starting from the corresponding ketones or alkenes. See, for instance: a) R. D. Patil, G. Joshi, S. Adimurthy, B. C. Ranu, Tetrahedron Lett. 2009, 50, 2529-2532;
    • (2009) Tetrahedron Lett. , vol.50 , pp. 2529-2532
    • Patil, R.D.1    Joshi, G.2    Adimurthy, S.3    Ranu, B.C.4
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    • 4 buffer pH 10 showed that only α-bromo ketone was unstable, while derivatives 2a and 3a did not decompose (see Supporting Information)
    • 4 buffer pH 10 showed that only α-bromo ketone was unstable, while derivatives 2a and 3a did not decompose (see Supporting Information).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.