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33947085164
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3 coupling constants, was erroneously based on the consideration of stronger intramolecular hydrogen bonds in the threo comparatively to the erythro adducts, see: House, H. O.; Crumrine, D. S.; Teranishi, A. Y.; Olmstead, H. D. J. Am. Chem. Soc. 1973, 95, 3310.
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-
41
-
-
0038421140
-
-
note
-
3) = 10.4 Hz] were carefully measured by peak pickings.
-
-
-
-
43
-
-
0038759138
-
-
note
-
2 250.1389).
-
-
-
-
44
-
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0038421132
-
-
note
-
Base-induced Peterson olefination of cyclopropanols 9a and 11a led to ring-opened derivatives (see ref. 1).
-
-
-
-
45
-
-
0038421139
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-
note
-
3) 178 (100), 161 (22), 160 (17), 159 (14), 143 (18), 131 (13).
-
-
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47
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0038082433
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PhD Thesis; Université de Paris-Sud: Orsay France
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Ollivier, J. PhD Thesis; Université de Paris-Sud: Orsay France, 1986.
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(1986)
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Ollivier, J.1
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49
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0038421141
-
X-ray crystallographic data of the diol 9a′
-
will be published
-
X-ray crystallographic data of the diol 9a′, will be published in Zeitschrift fuer Kristallographie.
-
Zeitschrift fuer Kristallographie
-
-
-
50
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0001244323
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+ force field) and semi-empirical ZINDO calculations have been performed with the Hyperchem software (version 5.1). The Ti-O and Ti-C bond lengths and the Ti-bond angles were in accord with reported RX data for titanium complexes. See: Gais, H. J.; Volhardt, J.; Linder, H. J.; Paulus, H. Angew. Chem., Int. Ed. Engl. 1988, 27, 1541.
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Angew. Chem., Int. Ed. Engl.
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Gais, H.J.1
Volhardt, J.2
Linder, H.J.3
Paulus, H.4
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