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0010541988
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J. Chem. Soc. Perkin Trans. 1
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Govindachari, T.1
Nagarajan, K.2
Parthasarathy, P.C.3
Rajagopalan, T.G.4
Desai, H.K.5
Kartha, G.6
Chen, S.L.7
Nakanishi, K.8
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15
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84984298398
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Von molekularen Wirten und Gästen sowie ihren Komplexen (Nobel-Vortrag)
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Angewandte Chemie
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Cram, D.J.1
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35
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84990132518
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(1987)
C. A.
, vol.107
, pp. 96106r
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36
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0000840987
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Synthesis of 1,1'-, 2,2'-, 1,2'-, and 2,6'-biazulenes and their derivatives by Ullmann reaction.
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(1982)
Bulletin of the Chemical Society of Japan
, vol.55
, pp. 1144
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Morita, T.1
Takase, K.2
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37
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84990170066
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For exceptions see e.g. [24]
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68
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84985615968
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Schlüsselbausteine der Naturstoff-Biosynthese und ihre Bedeutung für Chemie und Medizin
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(1979)
Angewandte Chemie
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Franck, B.1
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112
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84918678077
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Nickel and palladium complex catalyzed cross-coupling reactions of organometallic reagents with organic halides
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(1980)
Pure and Applied Chemistry
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, pp. 669
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Kumada, M.1
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122
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0000103227
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Palladium-katalysierte Kupplungsreaktionen organischer Elektrophile mit Organozinn-Verbindungen
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Angewandte Chemie
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Stille, J.K.1
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138
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84970602018
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The Stereoisomers of 5-Bromo-6,8-dimethoxy-1,2,3-trimethyl-1,2,3,4-tetrahydroisoquinoline. X-Ray Crystal-Structure of thetransIsomer
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(1990)
Australian Journal of Chemistry
, vol.43
, pp. 79
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Rizzacasa, M.A.1
Sargent, M.V.2
Skelton, B.W.3
White, A.H.4
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151
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84990098928
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In the case of very electron‐poor aromatic compounds (such as oxazoline‐substituted quinolines) the electrophilic coupling partner does not require a nucleofugal group
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167
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84990098188
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In another example, an unnatural but biologically more active aza‐analogous dibenzocyclooctadiene, the thermodynamic equilibrium even lies at only 1:40
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183
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84990145541
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A further advantage of this process is that apart from 42 and 43 hydroxymethyl compounds of type 41 and lactones of type 40 are found as natural products in the same plants and can thus be included synthetically without additional effort:, Planta med. 56
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(1990)
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Bringmann, G.1
Rübenacker, M.2
Jansen, J.R.3
Gender, T.4
Aké Assi, L.5
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184
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84990107761
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In contrast, precomplexation of the alkali metal cation of basic hydride transfer reagents at nitrogen and attack of the anionic hydride part of the reagent from the same side (i.e. from above) should lead to the other lactolate diastercomer (not shown in Scheme 27), which bears the hydrogen in β‐position; this isomer should react in an analogous manner to give 45b.
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187
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84990105156
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See for example the non‐stereoselective synthesis of a (probably not separable) mixture of all four possible stereoisomeric ancistrocladisines [113].
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