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For reviews, see: (a) Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993. (b) Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley: New York, 1994. (c) Brunner, H.; Zettimeier, W. Handbook of Enantioselective Catalysis with Transition Metal Compounds; VCH: Weinheim, Germany, 1993.
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For reviews, see: (a) Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993. (b) Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley: New York, 1994. (c) Brunner, H.; Zettimeier, W. Handbook of Enantioselective Catalysis with Transition Metal Compounds; VCH: Weinheim, Germany, 1993.
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-
34
-
-
85033170569
-
-
note
-
26-FeOPRh: C, 60.84; H, 4.43. Found: C, 60.59; H, 4.08.
-
-
-
-
35
-
-
85033168074
-
-
note
-
w = 0.023 for 4109 unique reflections (I > 3σ(I)).
-
-
-
-
36
-
-
85033182901
-
-
note
-
2Ru·2EtOH: C, 64.34; H, 5.61. Found: C, 64.10; H, 5.28.
-
-
-
-
37
-
-
85033189847
-
-
note
-
w = 0.084 for 3960 unique reflections (I > 3σ(I)).
-
-
-
-
38
-
-
0004005458
-
-
Houben-Weyl, Methods of Organic Chemistry E21a; Georg Thieme Verlag: Stuttgart, Germany
-
Stereoselective Synthesis; Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.; Houben-Weyl, Methods of Organic Chemistry E21a; Georg Thieme Verlag: Stuttgart, Germany, 1995.
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(1995)
Stereoselective Synthesis
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Helmchen, G.1
Hoffmann, R.W.2
Mulzer, J.3
Schaumann, E.4
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39
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0001818624
-
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Kataoka, Y.; Saito, Y.; Nagata, K.; Kitamura, K.; Shibahara, A.; Tani. K. Chem. Lett. 1995, 833.
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Tani, K.6
-
40
-
-
85033175224
-
-
note
-
3Ru: C, 61.58; H, 4.51. Found: C, 61.19; H, 4.89.
-
-
-
-
41
-
-
85033163318
-
-
note
-
-1, R = 0.078, Rw = 0.085 for 1944 unique reflections (I > 3σ(I)). The carbon atoms of cyclopentadienyl rings and ruthenium, iron, and phosphine atoms were refined anisotropically. All other non-hydrogen atoms were refined isotropically.
-
-
-
-
42
-
-
1142274757
-
-
(a) Davies, S. G.; McNally, J. P.; Smallridge, A. J. Adv. Organomet. Chem. 1990, 30, 1.
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-
46
-
-
85033181820
-
-
note
-
The low yield of 7 for both the stoichiometric and catalytic reactions was due to the formation of unidentified side products.
-
-
-
-
47
-
-
85033183458
-
-
note
-
The preliminary results of a few catalytic reactions using 5 are as follows: 1-octyne and 1-buten-3-ol (20%, 34% ee), 1-octyne and 4-methyl-1-penten-3-ol (10%, 27% ee). The results will be reported in due course.
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