By James Ralph Hanson; et al

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Umemoto, T. Tsuneya, and M. Shiga, Agric. and Biol. Chem. (Japan),1975,39,2083 (inadvertently omitted from last year’s Report); K. Umemoto and T. Nagasawa, Nagoya Gakuin University Review, 1976, 12, 117; T. Nagasawa, K. Umemoto, and N. Hirao, Nippon Nogei Kagaku Kaishi, 1977, 51, 81. J. Wiemann and Y. Dubois, Bull. Soc. chim. France, 1962, 1813. R. K. Thappa, K. L. Dhar, and C. K. 15, 1568. r. s. g. see Vol. 6 , p. r. and Raman spectra of limonene, p-menth-1-ene, trans-isolimonene, p-menth-3ene, and trans-p-menth-2-ene have been a n a l y ~ e d .

K. Itoh, M. S. Chem. , 1977, 500; reference 3 of this paper should refer to p. 4925 and not p. 492. P. J. R. Nederlof, M. J. Moolenaar, E. R. de Waard, and H. 0. Huisman, Tetrahedron, 1977, 33, 579. A. Musco, J. Mol. Catalysis, 1975/1976,1, 443. cta-2,7-dien-l-ol and 2,7-dimethylocta-l,7-dien-3-ol, or to various acetates depending upon the palladium catalyst/water/acetic acid/C02 . ratio,205 dimerization to (37) exclusively or with accompanying 8-alkoxy-2,7-dimethylocta- 1,6-diene and 3alkoxy-2,7-dimethylocta- 1,7-diene (palladium catalysts-alcohols) (cf.

A. Matos, and J. W. de Alencar, J. Chem. , 1976,53, 652. ''' ( a ) A. M. Humphrey, J. H. Greaves, B. E. Kent, W. S. Matthews, D. A. Moyler, R. G. Perry, J. Ridlington, R. A. Stocks, and G. Watson, Analyst, 1977,102,607; C. L. Goodwin and A. E. Squillace, Phytochemistry, 1976,15,1771; (b)C. H. Brieskorn and W. Schlicht, Pharm. , 1976,51,133. 176 J. Calderon, J. L. Munoz, L. Quijano, and T. Rios, Rev. Latinoamer. , 1976,7, 114 (Chem. , 1977,86,47 204). 177 E. V. C. International Symposium on the Chemistry of Natural Products, Dunedin, New Zealand, 1976, Abstract D27.

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