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Volumn 5, Issue 5, 1999, Pages 1565-1569

A substrate-based methodology that allows the regioselective control of the catalytic aminohydroxylation reaction

Author keywords

Amino alcohols; Aminohydroxylations; Osmium; Oxidations

Indexed keywords

AMINO ACID; AMINOALCOHOL;

EID: 0032912625     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3765(19990503)5:5<1565::AID-CHEM1565>3.0.CO;2-J     Document Type: Article
Times cited : (48)

References (37)
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    • a) J. Rudolph, P. C. Sennhenn, C. P. Vlaar, K. B. Sharpless, Angew. Chem. 1996, 108, 2991; Angew. Chem. Int. Ed. Engl. 1996, 35, 2810; b) G. Li, H. H. Angert, K. B. Sharpless, Angew. Chem. 1996, 108, 2995; Angew. Chem. Int. Ed. Engl. 1996, 35, 2813; c) M. Bruncko, G. Schlingloff, K. B. Sharpless, Angew. Chem. 1997, 109, 1580; Angew. Chem. Int. Ed. Engl. 1997, 36, 1483;
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    • Sharpless et al. observed a reversal of the regiochemistry between the PHAL- and the AQN-based ligands in the AA reaction of transcinnamate derivatives (ligand-based regioselective control). B. Tao, G. Schlingloff, K. B. Sharpless, Tetrahedron Lett. 1998, 39, 2507.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.