Folgen
Byung Tae Cho
Byung Tae Cho
Bestätigte E-Mail-Adresse bei hallym.ac.kr
Titel
Zitiert von
Zitiert von
Jahr
Direct and indirect reductive amination of aldehydes and ketones with solid acid-activated sodium borohydride under solvent-free conditions
BT Cho, SK Kang
Tetrahedron 61 (24), 5725-5734, 2005
2512005
Recent development and improvement for boron hydride-based catalytic asymmetric reduction of unsymmetrical ketones
BT Cho
Chemical Society Reviews 38 (2), 443-452, 2009
1592009
Recent advances in the synthetic applications of the oxazaborolidine-mediated asymmetric reduction
BT Cho
Tetrahedron 62 (33), 7621-7643, 2006
1592006
Selective reductions. 40. A critical examination of the relative effectiveness of various reducing agents for the asymmetric reduction of different classes of ketones
HC Brown, WS Park, BT Cho, PV Ramachandran
The Journal of Organic Chemistry 52 (24), 5406-5412, 1987
1371987
Chiral synthesis via organoboranes. 15. Selective reductions. 42. Asymmetric reduction of representative prochiral ketones with potassium 9-O-(1, 2: 5, 6-di-O-isopropylidene …
HC Brown, BT Cho, WS Park
The Journal of Organic Chemistry 53 (6), 1231-1238, 1988
1041988
Solvent-free reduction of aldehydes and ketones using solid acid-activated sodium borohydride
BT Cho, SK Kang, MS Kim, SR Ryu, DK An
Tetrahedron 62 (34), 8164-8168, 2006
832006
Application of optically active 1, 2-diol monotosylates for synthesis of β-azido and β-amino alcohols with very high enantiomeric purity. Synthesis of enantiopure (R …
BT Cho, SK Kang, SH Shin
Tetrahedron: Asymmetry 13 (11), 1209-1217, 2002
762002
Enantioselective synthesis of optically active secondary amines via asymmetric reduction
BT Cho, YS Chun
Tetrahedron: Asymmetry 3 (12), 1583-1590, 1992
701992
Boron‐Based Reducing Agents for the Asymmetrical Reduction of Functionalized Ketones and Ketimines
BT Cho
ChemInform 34 (17), no-no, 2003
552003
Efficient synthesis of optically active β-hydroxy p-tolylsulfones with very high enantiomeric excess via CBS–oxazaborolidine-catalyzed borane reduction
BT Cho, DJ Kim
Tetrahedron: Asymmetry 12 (14), 2043-2047, 2001
552001
Enantioselective addition of diethylzinc to aldehydes catalyzed by a new chiral β-amino alcohol derived from d-mannitol
BT Cho, YS Chun
Tetrahedron: Asymmetry 9 (9), 1489-1492, 1998
531998
Enantioselective addition of diethylzinc to aldehydes using γ-aminoalcohols derived from α-D-xylose as new chiral catalysts
BT Cho, N Kim
Tetrahedron letters 35 (24), 4115-4118, 1994
491994
Asymmetric reduction of. alpha.-keto esters with potassium 9-O-(1, 2: 5, 6-di-O-isopropylidene-. alpha.-D-glucofuranose)-9-boratabicyclo [3.3. 1] nonane. Chiral synthesis of …
HC Brown, BT Cho, WS Park
The Journal of Organic Chemistry 51 (17), 3396-3398, 1986
481986
Enantioselective synthesis of optically active β-aminoalcohols via asymmetric reduction
BT Cho, YS Chun
Tetrahedron: Asymmetry 3 (3), 341-342, 1992
441992
Clean and simple chemoselective reduction of imines to amines using boric acid-activated sodium borohydride under solvent-free conditions
BT Cho, SK Kang
Synlett 2004 (09), 1484-1488, 2004
412004
Facile synthesis of terminal 1, 2-diols with high optical purity via oxazaborolidine-catalyzed asymmetric borane reduction
BT Cho, YS Chun
The Journal of Organic Chemistry 63 (15), 5280-5282, 1998
401998
Facile synthesis of chiral isopropyl carbinols with high enantiomeric excess via catalytic enantioselective addition of diisopropylzinc to aldehydes
WK Yang, BT Cho
Tetrahedron: Asymmetry 11 (14), 2947-2953, 2000
392000
Highly efficient synthesis of chiral β-hydroxy sulfides with high enantiomeric purity via CBS-oxazaborolidine-catalyzed borane reduction
BT Cho, OK Choi, DJ Kim
Tetrahedron: Asymmetry 13 (7), 697-703, 2002
382002
A practical method for synthesis of terminal 1, 2-diols in high enantiomeric excess via oxazaborolidine-catalyzed asymmetric reduction
BT Cho, YS Chun
Tetrahedron: Asymmetry 10 (10), 1843-1846, 1999
381999
Addition compounds of alkali metal hydrides. 28. Preparation of potassium dialkoxymonoalkylborohydrides from cyclic boronic esters. A new class of reducing agents
HC Brown, WS Park, JS Cha, BT Cho, CA Brown
The Journal of organic chemistry 51 (3), 337-342, 1986
381986
Das System kann den Vorgang jetzt nicht ausführen. Versuchen Sie es später erneut.
Artikel 1–20