Preparation of Heteroatom Compounds by Stepwise Atom/Group Transfer incis- andtrans-[OsVI(tpy)(Cl)2(N)]+

2001 ◽  
Vol 40 (20) ◽  
pp. 5062-5063 ◽  
Author(s):  
My Hang V. Huynh ◽  
Donald L. Jameson ◽  
Thomas J. Meyer
Keyword(s):  
Group Transfer ◽  
Atom Group ◽  
Heteroatom Compounds

ChemInform Abstract: Metalloporphyrin-Catalyzed Asymmetric Atom/Group Transfer Reactions

ChemInform ◽  
2013 ◽  
Vol 44 (19) ◽  
pp. no-no
Author(s):  
Joshua V. Ruppel ◽  
Kimberly B. Fields ◽  
Nicole L. Snyder ◽  
X. Peter Zhang
Keyword(s):  
Transfer Reactions ◽  
Group Transfer ◽  
Atom Group

Metalloporphyrin-Catalyzed Asymmetric Atom/Group Transfer Reactions

2010 ◽  
pp. 1-84 ◽  
Author(s):  
Joshua V. Ruppel ◽  
Kimberly B. Fields ◽  
Nicole L. Snyder ◽  
X. Peter Zhang
Keyword(s):  
Transfer Reactions ◽  
Group Transfer ◽  
Atom Group

ChemInform Abstract: Practical Iron-Catalyzed Atom/Group Transfer and Insertion Reactions

ChemInform ◽  
2012 ◽  
Vol 43 (50) ◽  
pp. no-no
Author(s):  
Toby Wai-Shan Chow ◽  
Guo-Qiang Chen ◽  
Yungen Liu ◽  
Cong-Ying Zhou ◽  
Chi-Ming Che
Keyword(s):  
Insertion Reactions ◽  
Group Transfer ◽  
Atom Group

scholarly journals Practical iron-catalyzed atom/group transfer and insertion reactions

2012 ◽  
Vol 84 (8) ◽  
pp. 1685-1704 ◽  
Author(s):  
Toby Wai-Shan Chow ◽  
Guo-Qiang Chen ◽  
Yungen Liu ◽  
Cong-Ying Zhou ◽  
Chi-Ming Che
Keyword(s):  
Catalytic Reactions ◽  
Donor Ligands ◽  
Insertion Reactions ◽  
Group Transfer ◽  
Atom Group ◽  
Fe Complexes ◽  
Working Principle ◽  
Catalyzed Reactions ◽  
Epoxidation Of Alkenes

Iron-catalyzed reactions are receiving a surge of interest owing to the natural abundance and biocompatibility of Fe and the urge to develop practically useful sustainable catalysis for fine chemical industries. This article is a brief account of our studies on the C–O and C–N bond formation reactions catalyzed by Fe complexes supported by oligopyridine, macrocyclic tetraaza, and fluorinated porphyrin ligands. The working principle is the in situ generation of reactive Fe=O and Fe=NR intermediates supported by these oxidatively robust N-donor ligands for oxygen atom/nitrogen group transfer and insertion reactions. The catalytic reactions include C–H bond oxidation of saturated hydrocarbons (up to 87 % yield), epoxidation of alkenes (up to 96 % yield), cis-dihydroxylation of alkenes (up to 99 % yield), epoxidation–isomerization (E–I) reaction of aryl alkenes (up to 94 % yield), amination of C–H bonds (up to 95 % yield), aziridination of alkenes (up to 95 % yield), sulfimidation of sulfides (up to 96 % yield), and amide formation from aldehydes (up to 89 % yield). Many of these catalytic reactions feature high regio- and diastereoselectivity and/or high product yields and substrate conversions, and recyclability of the catalyst, demonstrating the applicability of Fe-catalyzed oxidative organic transformation reactions in practical organic synthesis.

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