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Crawford, L., Cole-Hamilton, D. J. & Buehl, M. Uncovering the mechanism of homogeneous methyl methacrylate formation with p,n chelating ligands and palladium: favored reaction channels and selectivities. Organometallics 34, 438–449 (2015). a) Golding, S., Katritzky, A. R. and Kucharska, H. Z. J. chem. Soc. (1965) 3090; Katritzky, A. R., with Kucharska, H. Z. and Rowe, T. D. ibid. 3093; ( b) with Reavill, R. E. ibid. 3825 Johnson, G. D., Katritzky, A. R., Ridgewell, B. J., Shakir, N. and White, A. M. Tetrahedron 31 (1965) 1055

Hamer, J., Link, W. J., Jurjevich, A. and Vigo, T. L. Recl Trav. chim. Pays-Bas Belg. 81 (1962) 1058 Helferich, B. with Moog, L. and Jünger, A. 58 (1925) 872; with Sieber, H. 59 (1926) 600; Rebek, M. 62 (1929) 2508; with Kramaršic, V. ibid. All Wibaut, J. P., Uhlenbroek, J. H., Kooyman, E. G. and Kettenes, D. K. Recl Trav. chim. Pays-Bas Belg. 79 (1960) 481 d) den Hertog, H. J., van der Does, L. and Landheer, C. A. Recl Trav. chim. Pays-Bas Belg 81 (1962) 864 d) Eddy, N. B., Murphy, J. G. and May, E. L. ibid. 1370; ( e) May, E. L. and Ager, J. H. 24 (1959) 1432; ( f) 25 (1960) 984; ( g) Fullerton, S. E., Ager, J. H. and May, E. L. 27 (1962) 2554a) Murakami, M. and Matsumura, E. J. chem. Soc. Japan (Pure Chem.) 70 (1949) 393; ( b) Matsumura, E. 74 (1953) 446; Lukeš, R. Colin. Czech. chem. Commun. 12 (1947) 71; with Pliml, J. 15 (1950) 463; and Jizba, J. and Štep, V. 19 (1954) 949

Any statement as to authorship, attribution, origin, date, age, provenance and condition is a statement of our opinion and is not to be taken as a statement of fact. a) Popov, A. I. with Pflaum, R. T. J. Am. chem. Soc. 79 (1957) 570; ( b) with Rygg, R. H. ibid. 4622Insurance: – All goods will be held insured against the risks of fire, burglary and water damage, for which Richard Winterton Auctioneers Ltd will charge a premium of 1% subject to the Value Added Tax. The value of the goods so covered shall be the gross amount realised, or in the case of unsold lots the best bid, or in the case of withdrawn lots prior to a sale that which the specialised staff of Richard Winterton Auctioneers Ltd shall in their absolute discretion, estimate to be the auction value of the goods. a) Jaffé, H. H. and Jones, H. L. J. org. Chem. 30 ( Eastham, G. R. et al. Synthesis and spectroscopic characterisation of the intermediates in the Pd-catalysed methoxycarbonylation of ethene. Chem. Commun. 7, 609–610 (2000). Relationship of the Dromedary TRDV Germline Genes with Public Available Gene Sequences and Analysis of the δ-Chain Repertoire I went to a paint shop (who is my customer too), They opened to software and showed me that it is a mixture of pure white paint (99%) with a few drops of blue and other colors.

Besides their adaptation to harsh environments, camels are multipurpose animals used for milk and meat production, racing, transportation and tourism. Despite the somatic mutation, we tentatively evaluated the contribution of each annotated germline genes in the formation of the δ chain repertoire with particular reference to the CDR3-IMGT region. A total of 61 cDNA clones isolated from peripheral lymphoid tissues of an adult healthy dromedary (22 from spleen, 15 from tonsils and 24 from blood) and containing unique rearranged productive V–(D)–J–C transcripts, were selected from the cDNA library [ 5] and analysed. Penfold, B. R. Acta crystallogr. 6 (1953) ( a) 591 ( b) 707; ( c) Wright, W. B. and King, G. D. S. ibid. 305 To develop the first general alkoxycarbonylation catalyst for ‘non-reactive’ olefins, we focused on the alkoxycarbonylation of tetramethylethylene 1a as the benchmark substrate. In our initial attempts, we performed catalytic experiments with two state-of-the-art palladium catalysts: Pd 2(dba) 3/ L1/MeSO 3H (refs 10, 11, 29) known from the methyl methacrylate process developed by Eastham et al. and established by Lucite International and the Shell system Pd(OAc) 2/ L2/MeSO 3H pioneered by Drent and co-workers for the methoxycarbonylation of alkynes 30, 31, 32, 33, 34, 35. However, in both cases no carbonylation occurred and only the corresponding ether—resulting from electrophilic addition of methanol—was detected in 50 and 45% yield, respectively. Obviously, to realize the alkoxycarbonylation of 1a, the development of a new catalyst system is imperative. According to the so-called hydride mechanism (see Supplementary Fig. 1 for details), successful alkoxycarbonylation requires the formation of a palladium hydride complex 26, 36, 37, 38, 39. a) Ochiai, E., Itai, T. and Yoshino, K. Proc. imp. Acad. Japan 20 (1944) 141; ( b) Katritzky, A. R. J. chem. Soc. (1956) 2404

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Carlsohn, H. Ber. dtsch. chem. Ges. 68 (1935) 2209; Über eine neue Klasse von Verbindungen des positiv einwertigen Jods, Leipzig, 1932 Surrey, A. R. and Lindwall, H. G. J. Am. chem. Soc. 62 (1940) 1697; Boarland, M. P. V. and McOmie, J. F. W. J. chem. Soc. (1951) 1218; a) Bishop, R. R., Cavell, E. A. S. and Chapman, N. B. J. chem. Soc. (1952) 437; ( b) the latter two, (1953) 3392 Richard Winterton Auctioneers Ltd reserve the right to store or arrange the the storage of goods delivered to them for sale either on their own premises or elsewhere at their sole discretion. They exempt themselves from any liability for loss or damage to goods delivered without sufficient sale instructions. All dimensions are given in centimetres, height before width and are approximate. Pictures are unframed unless otherwise stated.