By J R Hanson; James Ralph Hanson; Royal Society of Chemistry (Great Britain); et al
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Extra info for A review of the literature published between September 1975 & August 1976
Sakuda, Yukagaku, 1976,25, 161; ambiguities in the English abstract are resolved by reference to Table 1. 310 T. Tahara and Y. Sakuda, Yukagaku, 1 9 7 5 , 2 4 , 4 4 6 . 331 ( a ) V. P. Yur'ev, 1. Gailyunas, L. V. Spirikhin, and G. A. Tolstikov, Zhur. , 1975, 45, 2312; ( 6 )cf. E. E. Royals and J. C. Leffingwell, J. Org. , 1966,31, 1937, and Vol. 1, p. 26, ref. 91. See also Vol. 4, p. 57, ref. 269. 312 K. Arata and K. Tanabe, Chem. Letters, 1976, 321. 313 K . Arata, S. Akutagawa, and K. Tanabe, J.
1976, B32, 500; see F. Baert and R. Fouret, Cryst. , 1975, 4, 307. D. Rogers, J. M. Franco, S. Martinez-Carrera,and S. , 1975, B31, 2742. zng Y. Senda and S. Imaizumi, Tetrahedron, 1975, 31, 2905. Terpenoids and Steroids 30 unusually high binding potential of the r-bond in the photoelectron spectrum of ascaridole may be due to electronegativity Kinetic data are reported for acid-catalysed addition of acetic acid to l i m ~ n e n e . ~ ~ ’ Alkylation of isovaleramide with 1,3-dichlorobut-2-ene yields (139) after methylation; acid-catalysed hydrolysis and internal aldol condensation gives ( )~ i p e r i t o n e .
981 695 (Chem. A h . , 1976, 85, 33 220). 301 T. Shono and Y. Takagi, Jap. P. 69 049/1975 (Chem. A h . , 1975,83, 193 551). 290 29l Monoterpenoids 31 Last year's Report of (+)-limonene hydroboration (Vol. 6, p. 30) did not refer to the earlier Report (Vol. 3, p. 35) which, in the case of Brown's work, is a repetition of earlier Bacdyshev reports the salicylic acid-catalysed rearrangement of isoterpinolene to various p-methadienes (cf. Vol. 3, p. 71, ref. 304 Pyrolysis of limonene diacetate yields perillyl acetate as the major The full paper on the oxidation of cis- and trans-p-menth-2-ene with t-duty1 perbenzoate-cupric octanoate has appeared (Vol.
A review of the literature published between September 1975 & August 1976 by J R Hanson; James Ralph Hanson; Royal Society of Chemistry (Great Britain); et al