Kendal

G. D. Halsey, see Twenty Years of Colloid and Surface Chemistry The Kendall Award Adresses, Amer. Chem. Soc., Washington, DC, 1973. 

Johnson K L, Kendall K and Roberts A D 1971 Surface energy and the contact of elastic solids Proc. R. Soc. A 324 301... 

Chalasinski G, Kendall R A, Taylor H and Simons J 1988 Propensity rules for vibration-rotation induced electron detachment of diatomic anions application to NH -> NH + e J. Phys. Chem. 92 3086-91... 

Simons J 1981 Propensity rules for vibration-induced electron detachment of anions J. Am. Chem. See. 103 3971-6 Acharya P K, Kendall R A and Simons J 1984 Vibration-induced electron detachment in molecular anions J. Am. Chem. See. 106 3402-7... 

Kendall structure Kenics mixer Ken-React KR TTS Kentucky bluegrass Kenyaite [12285-95-9]... 

W. A. Zisman, in K. J. Mysels and co-workers, eds., 20 Years of Suface and Colloid Chemistry, The Kendall Award Addresses, American Chemical Society, Washington, D.C., 1973, p. 109. 

Other companies with early involvement in developing nonwovens as textile replacements include Avondale Mills, Kimberly-Clark, The Kendall Company, and the West Point Manufacturing Company. Freudenburg of Germany, a worldwide producer of nonwoven interlinings (another woven fabric replacement), began efforts in the 1930s to find a substitute for leather (qv) (7). 

J. D. Kendall, in L. P. Clerc, ed., ISP Congms Internationalde Photographie Scientifique et Appliquue, Paris 1935, Editions Revue d Optique, Paris, 1936, p. 

Since fV-acylpyrazoles have been fully described in (B-76MI40402) only a summary and some new references will be discussed here. Only neutral pyrazolides have been described, but a cationic intermediate (249) is involved in the Olofson and Kendall method of obtaining minor fV-alkylated isomers (70JOC2246). 

The fact that the isomeric structure of azolides is thermodynamically controlled has been used by Olofson and Kendall to prepare 1-alkylazoles regioselectively (70JOC2246). An asymmetric pyrazole yields two alkylated derivatives (Scheme 21 see Section 4.04.2.1.3 (viii)), but the alkylation with a powerful alkylating agent of the acetylated derivative leads to the less abundant isomer via the salt (249), which is too unstable to be isolated. 

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