Quantum chemical modeling of chiral catalysis. Part 15. On the role of hydride-bridged borane - alkoxyborane complexes in the catalytic enantioselective reduction of ketones promoted by chiral oxazaborolidines

Vesa Nevalainen

doi:10.1016/s0957-4166(00)86186-8

Quantum chemical modeling of chiral catalysis. Part 15. On the role of hydride-bridged borane - alkoxyborane complexes in the catalytic enantioselective reduction of ketones promoted by chiral oxazaborolidines

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)86186-8 ◽

1994 ◽

Vol 5 (2) ◽

pp. 289-296 ◽

Cited By ~ 9

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Reduction Of Ketones

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Quantum chemical modeling of chiral catalysis. Part 13. On the role of borane O-adducts in the enantioselective reduction of ketones catalyzed by chiral oxazaborolidines

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)82249-1 ◽

1993 ◽

Vol 4 (9) ◽

pp. 2001-2010 ◽

Cited By ~ 12

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Reduction Of Ketones

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Quantum chemical modeling of chiral catalysis. Part 8. On the conformational freedom of the ketone of ketone-borane complexes of oxazaborolidines used as catalysts in the enantioselective reduction of ketones

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)86061-9 ◽

1992 ◽

Vol 3 (12) ◽

pp. 1563-1572 ◽

Cited By ~ 31

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Conformational Freedom ◽

Reduction Of Ketones

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Quantum chemical modeling of chiral catalysis. Part 16. On the isomerism of dimers of chiral oxazaborolidines used in the catalytic enantioselective reduction of ketones

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)86210-2 ◽

1994 ◽

Vol 5 (3) ◽

pp. 387-394 ◽

Cited By ~ 3

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Reduction Of Ketones

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Quantum chemical modeling of chiral catalysis. Part 7. On the effects controlling the coordination of borane to chiral oxazaborolidines used as catalysts in the enantioselective reduction of ketones

Tetrahedron Asymmetry ◽

10.1016/0957-4166(92)80021-n ◽

1992 ◽

Vol 3 (11) ◽

pp. 1441-1453 ◽

Cited By ~ 33

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Reduction Of Ketones

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Quantum chemical modeling of chiral catalysis. Part 3. On the role of a Lewis basic solvent in the mechanism of catalytic enantioselective reduction of carbonyl compounds by chiral oxazaborolidines

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)80466-8 ◽

1991 ◽

Vol 2 (8) ◽

pp. 827-842 ◽

Cited By ~ 34

Author(s):

Vesa Nevalainen

Keyword(s):

Carbonyl Compounds ◽

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis

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Quantum chemical modeling of chiral catalysis. Part 11. Isomerism in borane adducts of chiral oxazaborolidines used as catalysts in the enantioselective reduction of ketones ?

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)80361-4 ◽

1993 ◽

Vol 4 (7) ◽

pp. 1569-1572 ◽

Cited By ~ 4

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Reduction Of Ketones

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Quantum chemical modeling of chiral catalysis. Part 17. On the diboranc derivatives of chiral oxazaborolidines used as catalysts in the enantioselective reduction of ketones

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)86211-4 ◽

1994 ◽

Vol 5 (3) ◽

pp. 395-402 ◽

Cited By ~ 3

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Derivatives Of ◽

Reduction Of Ketones

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Quantum chemical modeling of chiral catalysis. Part 19. Strain and stability - oxazadiboretanes potentially involved in the enantioselective reduction of ketones promoted by chiral oxazaborolidines

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)86242-4 ◽

1994 ◽

Vol 5 (5) ◽

pp. 903-908 ◽

Cited By ~ 18

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Reduction Of Ketones

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Quantum chemical modeling of chiral catalysis. Part 12. On the influence of the nature of the ring system on binding in ketone - borane complexes of chiral oxazaborolidines used as catalysts in the enantioselective reduction of ketones

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)80365-1 ◽

1993 ◽

Vol 4 (7) ◽

pp. 1597-1602 ◽

Cited By ~ 21

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Ring System ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Reduction Of Ketones

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Quantum chemical modeling of chiral catalysis. Part 9. On the aggregation reactions of borane and chiral oxazaborolidines used as catalysts in the enantioselective reduction of ketones

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)80352-3 ◽

1993 ◽

Vol 4 (7) ◽

pp. 1505-1519 ◽

Cited By ~ 9

Author(s):

Vesa Nevalainen

Keyword(s):

Quantum Chemical ◽

Quantum Chemical Modeling ◽

Chemical Modeling ◽

Enantioselective Reduction ◽

Chiral Catalysis ◽

Reduction Of Ketones

Download Full-text