-
1
-
-
0000353538
-
-
references therein
-
B.R. Bender, M. Koller, D. Nanz and W. Von Philipsborn, J. Am. Chem. Soc, 1993, 115, 5889 and references therein.
-
(1993)
J. Am. Chem. Soc
, vol.115
, pp. 5889
-
-
Bender, B.R.1
Koller, M.2
Nanz, D.3
Von Philipsborn, W.4
-
2
-
-
0000735257
-
-
B. McCulloch, J. Halpern, M.R. Thompson and C.R. Landis, Organometallics, 1990, 9, 1392.
-
(1990)
Organometallics
, vol.9
, pp. 1392
-
-
McCulloch, B.1
Halpern, J.2
Thompson, M.R.3
Landis, C.R.4
-
3
-
-
0003400107
-
Asymmetric catalysis in organic synthesis
-
Wiley-Interscience, New York, ch. 1
-
Asymmetric Catalysis in Organic Synthesis, ed. R. Noyori, Wiley-Interscience, New York, 1994, ch. 1.
-
(1994)
-
-
Noyori, R.1
-
6
-
-
0000935935
-
-
J.S. Giovannetti, C.M. Kelly and C.R. Landis, J. Am. Chem. Soc, 1993, 115, 4040.
-
(1993)
J. Am. Chem. Soc
, vol.115
, pp. 4040
-
-
Giovannetti, J.S.1
Kelly, C.M.2
Landis, C.R.3
-
7
-
-
84989141784
-
-
H. Bircher, B.R. Bender and W. Von Philipsborn, Magn. Reson. Chem., 1993, 31, 293.
-
(1993)
Magn. Reson. Chem
, vol.31
, pp. 293
-
-
Bircher, H.1
Bender, B.R.2
Von Philipsborn, W.3
-
8
-
-
37049069497
-
Further evidence from dynamic 31p nmr is on hand
-
Further evidence from dynamic 31P NMR is on hand. R. Kadyrov, T. Freier, D. Heller, M. Michalik and R. Selke, J. Chem. Soc, Chem. Commun., 1995, 1745.
-
(1995)
J. Chem. Soc, Chem. Commun
, pp. 1745
-
-
Kadyrov, R.1
Freier, T.2
Heller, D.3
Michalik, M.4
Selke, R.5
-
10
-
-
0027939311
-
-
J.A. Ramsden, J.M. Brown, M.B. Hursthouse and A.I. Karaulov, Tetrahedron Asymmetry, 1994, 5, 2033.
-
(1994)
Tetrahedron Asymmetry
, vol.5
, pp. 2033
-
-
Ramsden, J.A.1
Brown, J.M.2
Hursthouse, M.B.3
Karaulov, A.I.4
-
11
-
-
0001769326
-
-
J.M. Brown, P.L. Evans and A.P. James, Org. Synth., 1989, 68, 64.
-
(1989)
Org. Synth
, vol.68
, pp. 64
-
-
Brown, J.M.1
Evans, P.L.2
James, A.P.3
-
12
-
-
84943963535
-
-
E.g., and references therein in the present case the disfavoured Re-isomers correlate with the favoured S enantiomer of product, and e.e.s. of 80-85% are obtained
-
E.g. S.K. Armstrong, J.M. Brown and M.J. Burk, Tetrahedron Lett., 1993, 34, 689, and references therein in the present case the disfavoured Re-isomers correlate with the favoured S enantiomer of product, and e.e.s. of 80-85% are obtained.
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 689
-
-
Armstrong, S.K.1
Brown, J.M.2
Burk, M.J.3
-
13
-
-
0000164203
-
For recent applications of exsy to organometallic structure
-
see
-
For recent applications of EXSY to organometallic structure, see: M.T. Ashby, G.N. Govindan and A.K. Grafton, J. Am. Chem. Soc, 1994, 116, 4801.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 4801
-
-
Ashby, M.T.1
Govindan, G.N.2
Grafton, A.K.3
-
14
-
-
0001704975
-
-
A. Gogoll, J. Oernebro, H. Grennberg and J.E. Backvall, J. Am. Chem. Soc, 1994, 116, 3631.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 3631
-
-
Gogoll, A.1
Oernebro, J.2
Grennberg, H.3
Backvall, J.E.4
-
15
-
-
0039850797
-
-
E.W. Abel, E.S. Blackwall, K.G. Orrell and V. Sik, J. Organomet. Chem., 1994, 464, 163.
-
(1994)
J. Organomet. Chem
, vol.464
, pp. 163
-
-
Abel, E.W.1
Blackwall, E.S.2
Orrell, K.G.3
Sik, V.4
-
18
-
-
84987452290
-
Prepared as before (Ref. 2) but with an improved procedure for the synthesis of 13c-benzaldehyde as oxazolone precursor
-
cf.
-
Prepared as before (ref. 2) but with an improved procedure for the synthesis of 13C-benzaldehyde as oxazolone precursor, cf. H.C. Brown, C. Gundu Rao and S.U. Kulkarni, Synthesis, 1979, 704.
-
(1979)
Synthesis
, pp. 704
-
-
Brown, H.C.1
Gundu Rao, C.2
Kulkarni, S.U.3
|