Smaller substituents on nitrogen facilitate the osmium-catalyzed asymmetric aminohydroxylation

Angewandte Chemie - International Edition

Volumn 35, Issue 23-24, 1997, Pages 2810-2813

  Rudolph, Joachim ^a   Sennhenn, Peter C ^a   Vlaar, Cornelis P ^a   Sharpless, K Barry ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

Amino alcohols; Asymmetric aminohydroxylation; Catalysis; Chloramines; Sulfonamides

Indexed keywords

EID: 0030484752     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. a) G. Li, H.-T. Chang, K. B. Sharpless, Angew. Chem. 1996, 108, 449-452;
2. Angew. Chem. Int. Ed. Engl. 1996, 35, 451-454
3. b) G. Li, K. B. Sharpless, Acta Chem. Scand. 1996, 50, 649-651.
4. Certain functionalized alkylsulfonamides have recently been found to be interesting candidates for deprotection: a) S. M. Weinreb, D. M. Demko, T. A. Lessen, J. P. Demers, Tetrahedron Lett. 1986, 27, 2099-2102
5. b) T. Fukuyama, personal communication.