By J R Hanson; G Britton; Chemical Society.; et al
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Extra info for A review of the literature published between September 1977 and August 1978
W. Patrick, L. K. Truesdale, S. A. Biller, and K. B. Sharpless, J. Org. , 1978,43,2628. Two closely related papers (no monoterpenoid examples) report major improvements in this process, viz. E. Herranz and K. B. , 1978,43,2544; E. Herranz, S. A. Biller, and K. B. Sharpless, J. Amer. Chem. ,1978,100, 3596. g. 3 -endo -hydroxycamphor) using M O O ~ - ~ ~ - H M P A ; thermal '~' intermediate fragmentation may lead to some camphorquin~ne,~~' which is also a major by-product in attempted conversion of thiocamphor into camphor using benzeneseleninic anhydride as reagent.
1978, 43, 188. D. H. R. Barton, N. J. Cussans, and S. V. S. Chem. , 1978, 393. T. Hori and K. B. Sharpless, J. Org. , 1978, 43, 1689. H. Kropf and M. R. Yazdanbakhch, Synthesis, 1977,711. I. A. Gailyunas, E. M. Tsyrlina, N. I. Solov'eva, N. G. Komalenkova, and V. P. Yur'ev, J. Gen. Chem. ),1977,47,2188. However, see ref. 181; this compound is incorrectly named in the paper. K. Yamada, S. Goto, H. Nagase, Y. Kyotani, and Y. Hirata, J. Org. , 1978,43,2076. D. L. J. Clive and S. M. S. Chem. , 1977,658.
J . Cernigliaro and P. J . Kocienski, J. Org. , 1977, 42, 3622; this compound is named incorrectly in this paper. L. L. Danilov, L. V. Volkova, and R. P. 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.