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1
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0002874969
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Morrison, J. W.; Scott, J. W., Eds; Academic Press: New York
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Scott, J. W. In Asymmetric Synthesis; Morrison, J. W.; Scott, J. W., Eds; Academic Press: New York, 1984, Vol. 4, pp. 1-226.
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(1984)
In Asymmetric Synthesis
, vol.4
, pp. 1-226
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Scott, J.W.1
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2
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4444276636
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and references therein
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Kolb, H. C.; Van Nieuwenhze, M. S.; Sharpless, K. B. Chem. Rev. 1994, 94, 2483 and references therein.
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(1994)
Chem. Rev.
, vol.94
, pp. 2483
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Kolb, H.C.1
Van Nieuwenhze, M.S.2
Sharpless, K.B.3
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3
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0344536355
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McLaughlin, A. G. I.; Milton, R.; Perry, K. M. A. Brit. J. Ind. Med. 1946, 3, 183.
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(1946)
Brit. J. Ind. Med.
, vol.3
, pp. 183
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McLaughlin, A.G.I.1
Milton, R.2
Perry, K.M.A.3
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4
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84987678281
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Bortolini, O.; Fantin, G.; Fogagnolo, M.; Giovannini, P. P.; Guerrini, A.; Medici, A. J. Org. Chem. 1997, 62, 1854.
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(1997)
J. Org. Chem.
, vol.62
, pp. 1854
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Bortolini, O.1
Fantin, G.2
Fogagnolo, M.3
Giovannini, P.P.4
Guerrini, A.5
Medici, A.6
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6
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0344966983
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Eds; VCH: Weinheim
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Enzyme Catalysis in Organic Synthesis; Drauz, K.; Waldmann, H., Eds; VCH: Weinheim, 1995, Vol. II, p. 731.
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(1995)
Enzyme Catalysis in Organic Synthesis
, vol.2
, pp. 731
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Drauz, K.1
Waldmann, H.2
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7
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-
0030789621
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-
The combined yields of the recovered alcohol and the α-hydroxy ketone are always higher than 50%. For a recent report on the coupled use of resolution and recovery of the substrate see for example:
-
The combined yields of the recovered alcohol and the α-hydroxy ketone are always higher than 50%. For a recent report on the coupled use of resolution and recovery of the substrate see for example: Larsson, A. L. E.; Persson, B. A.; Backvall, J. E. Angew. Chem. Int. Ed. Engl. 1997, 36, 1211.
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(1997)
Angew. Chem. Int. Ed. Engl.
, vol.36
, pp. 1211
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Larsson, A.L.E.1
Persson, B.A.2
Backvall, J.E.3
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8
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-
84920311191
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-
Acyclic syn compounds are formed by the (R,R) and (S,S) pair, anti compounds by the (R,S) and (S,R) pair. With cyclic compounds the nomenclature is inverted: syn is the meso compound and anti is the (R,R) and (S,S) pair
-
Acyclic syn compounds are formed by the (R,R) and (S,S) pair, anti compounds by the (R,S) and (S,R) pair. With cyclic compounds the nomenclature is inverted: syn is the meso compound and anti is the (R,R) and (S,S) pair.
-
-
-
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9
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-
0029092875
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-
For selectivity as a function of steric bulkiness see
-
For selectivity as a function of steric bulkiness see Kim, M. J.; Choi, G. B.; Kim, J. Y.; Kim, H. J. Tetrahedron Lett. 1995, 36, 6253.
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(1995)
Tetrahedron Lett.
, vol.36
, pp. 6253
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Kim, M.J.1
Choi, G.B.2
Kim, J.Y.3
Kim, H.J.4
-
10
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-
84920311190
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-
The catalytic system is equally effective as a single enzyme, where BSDR catalyzes the desired reaction while simultaneously regenerating the cofactor. In this case, the BSDR natural substrate diacetyl i.e. (2,3-butandione) has been used as a cosubstrate, see Ref. 13. For an easy work-up of the reaction mixture, however, the double-enzyme system is recommended
-
The catalytic system is equally effective as a single enzyme, where BSDR catalyzes the desired reaction while simultaneously regenerating the cofactor. In this case, the BSDR natural substrate diacetyl i.e. (2,3-butandione) has been used as a cosubstrate, see Ref. 13. For an easy work-up of the reaction mixture, however, the double-enzyme system is recommended.
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-
-
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11
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0028343849
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Nicolosi, G.; Patti, A.; Piattelli, M.; Sanfilippo, C. Tetrahedron: Asymmetry 1994, 5, 283.
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(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 283
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Nicolosi, G.1
Patti, A.2
Piattelli, M.3
Sanfilippo, C.4
-
13
-
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0030220236
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Giovannini, P. P.; Medici, A.; Bergamini, C. M.; Rippa, M. Bioorg. Med. Chem. 1996, 4, 1197.
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(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 1197
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Giovannini, P.P.1
Medici, A.2
Bergamini, C.M.3
Rippa, M.4
-
16
-
-
0344966981
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-
(b) Eds; VCH: Weinheim
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(b) Enzyme Catalysis in Organic Synthesis; Drauz, K., Waldmann, H., Eds; VCH: Weinheim, 1995, Vol. I, p. 63.
-
(1995)
Enzyme Catalysis in Organic Synthesis
, vol.1
, pp. 63
-
-
Drauz, K.1
Waldmann, H.2
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17
-
-
84920311189
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-
For the optical rotation of the (S,S)-enantiomer see Ref. 4
-
For the optical rotation of the (S,S)-enantiomer see Ref. 4.
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-
-
-
18
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0000641488
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Sakai, T.; Nakagawa, Y.; Takahashi, J.; Iwabuchi, K.; Ishii, K. Chem. Lett. 1984, 263.
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(1984)
Chem. Lett.
, pp. 263
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Sakai, T.1
Nakagawa, Y.2
Takahashi, J.3
Iwabuchi, K.4
Ishii, K.5
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21
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-
84920311188
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-
Commercially available product
-
Commercially available product.
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-
-
-
22
-
-
0017815321
-
-
(a)
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(a) Kawabata, J.; Tahara, S.; Mizutani, J. Agric. Biol. Chem. 1978, 42, 89;
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Agric. Biol. Chem.
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, pp. 89
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Kawabata, J.1
Tahara, S.2
Mizutani, J.3
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23
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0001081787
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(b)
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(b) Bel-Rhlid, R.; Fauve, A.; Veschambre, H. J. Org. Chem. 1989, 54, 3221.
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(1989)
J. Org. Chem.
, vol.54
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Bel-Rhlid, R.1
Fauve, A.2
Veschambre, H.3
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