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By J R Hanson; G Britton; Chemical Society.; et al

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Evstigneeva, J. Gen. Chem. ),1977,47, 1948. H. Itokawa, K. Takeya, and S . Mihashi, Chem. and Pharm. Bull. (Japan),1977,25,1941;K. Takeya and H. , p. 1947. J. Rama Devi and P. K. Bhattacharyya, Indian J. Biochem. , p. 359.

G. Finke, P. L. Matlock, R. Wahren, R. G. Komoto, and J. I. Brauman, J. Amer. Chem. ,1978,100, 11 19; see Vol. 7, p. 7 for the earlier report. The authors also make a useful comparison with other methods for performing this reaction. 201 N. A. Cortese and R. F. Heck, J. Org. , 1978,43, 3985. 202 E. C. Ashby, A. B. Goel, and J. J. Lin, Tetrahedron Letters, 1977, 3133; E. C. Ashby, J. J. Lin, and A. B. Goel, J. Org. , 1978,43, 1560, 1564; cf Vol. 7, p. 7 . 203 W. Adam and H. J. Eggelte, Angew. Chem.

Ephritikhine, and H. Felkin, Nouueau J. , 1978, 2, 355. ''I W. E. Fristad, T. R. Bailey, and L. A. Paquette, J. Org. , 1978, 43, 1620. '" ( a ) S. L. Huang, K. Omura, and D. Swern, Synthesis, 1978, 297; ( 6 ) K. Omura and D. Swern, Tetrahedron, 1978,34,1651; (c) A. J. -L. Huang, andD. Swern, J. Org. , 1978,43, 2480. l B 3 H. Firouzabadi and E. Ghaderi, Tetrahedron Letters, 1978, 839; the borneols [a mixture of (+)-borne01 and (-)-isoborneol was used] and camphor each lack the C-10 methyl group in this paper.

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