The Preparation of Derivatives for the Identification of Alkyl Chlorides1
HW Underwood Jr, JC Gale
Index: Underwood; Gale Journal of the American Chemical Society, 1934 , vol. 56, p. 2117,2119
Full Text: HTML
Citation Number: 9
Abstract
Oct., 1934 DERIVATIVES FOR THE IDENTIFICATION OF ALKYL CHLORIDES 2117 the residue was taken up in dry acetone, filtered, run almost to dryness as above, taken up in water, the bitter principle salted out with ammonium sulfate, dissolved in acetone, again taken almost to dryness as above, taken up in 95y0 alcohol and diluted to volume with water. Its concentration was determined by means of Fehling's solution by 1 he Munson- ...
Related Articles:
[Nakatsuji, Hidefumi; Morimoto, Mami; Misaki, Tomonori; Tanabe, Yoo Tetrahedron, 2007 , vol. 63, # 48 p. 12071 - 12080]
[Funasaka, Setsuo; Mukaiyama, Teruaki Bulletin of the Chemical Society of Japan, 2008 , vol. 81, # 1 p. 148 - 159]
Metal-free oxidative amide formation with N-hydroxysuccinimide and hypervalent iodine reagents
[Yao, Haoyi; Tang, Yun; Yamamoto, Kana Tetrahedron Letters, 2012 , vol. 53, # 38 p. 5094 - 5098]
Malonic Ester Amide Synthesis: An Efficient Methodology for Synthesis of Amides
[Mahajan, Pankaj S.; Mahajan, Jyoti P.; Mhaske, Santosh B. Synthetic Communications, 2013 , vol. 43, # 18 p. 2508 - 2516]
Estrogen carcinogenesis in breast cancer
[Chen, I.-Li; Wang, Tai-Chi; Chen, Yeh-Long; Tzeng, Cherng-Chyi Journal of the Chinese Chemical Society, 2000 , vol. 47, # 1 p. 155 - 162]