CBS 60 Minutes

On CBS 60 Minutes, Kessler expressed his indignation, [the juice] was made from concentrate. My grandmother could have told you, I mean, it wasn t fresh. It wasn t very hard [to tell the difference]. ... 

Figure 5.8.B Cyanogen chloride poison gas delivered by mortar shells, Panama, 1944. Photographs by U.S. Army. Pictures obtained courtesy Archives CBS 60 Minutes.

Photographs by U.S. Army. Pictures obtained courtesy Archives CBS 60 Minutes. 

I am grateful to DeLorme, Street Atlas USA, for permission to print their maps as Figure I in Chapter 4, and to the Archives of CBS 60 Minutes for Figures 8 and 9 of Chapter 5. 

His charges generated public controversy 3 months later when he repeated them in an interview with the CBS television news magazine 60 Minutes broadcast on September 7, 1997. Other Russian officials initially dismissed Lebed s charges, saying all the country s nuclear weapons were accounted for and under strict control. Top-ranking Russian defense officials later went further and denied that the U.S.S.R. ever built such weapons, claiming they were too expensive to maintain and too heavy for practical use. 

In mid-1982 on the program "60 Minutes," CBS presented a somewhat frightening story of how water wells on Long Island, New York had been contaminated by the pesticide Temik, and that its use was proliferating, especially in Florida. The story parenthetically added that no one in Florida was monitoring for pesticides in groundwater, nor was anyone really aware of the pesticide Temik s contamination potential. 

U.S. plants open to terrorists, 60 Minutes broadcast on CBS, June 13, 2004. 

Compound 1567 CB and chloracetone are caused to react as in (B), the mineral salts subsequently filtered, 12 ml of concentrated hydrochloric acid are added to the solution in dimethyl formamide without dilution with water, and the mixture heated for 40 minutes on a water bath. The product crystallizes in the warm mixture, the mixture is cooled to room temperature, filtered, the residue washed with water and crystallized from acetic acid. MPc = 222°C. Yield 60% based on compound 1567 CB. 

C) Preparation of 2-Acetyl-3-Methyl-5-(2-Oxo-2,5-Dihydro-4-Furyl)Benro[b]Furan (3556 CB) (1) A suspension of 2 grams of the compound prepared according to (B) in 20 ml of concentrated hydrochloric acid, is heated to about 50°C, just until it dissolves. There after it is heated for 2 minutes to 70°C, just until precipitation commences. The mixture is allowed to cool, diluted with water, filtered, the residue washed, dried, and sublimed at 200°C and 0.1 mm pressure. 1.4 grams of product (Yield 70%) is obtained. MPc=218°-221°C. A second sublimation produces a chemically pure product. MPC= 221°-222°C. (2) Compound 1567 CB and chloracetone are caused to react as in (B), the mineral salts subsequently filtered, 12 ml of concentrated hydrochloric acid are added to the solution in dimethyl formamide without dilution with water, and the mixture heated for 40 minutes on a water bath. The product crystallizes in the warm mixture, the mixture is cooled to room temperature, filtered, the residue washed with water and crystallized from acetic acid. MPC= 222°C. Yield 60% based on compound 1567 CB. 

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