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chain products
Mechanisms of formation of the free-radical chain products are discussed.
      
Thus, variations in starting material and variations in procedure make possible a great variety of straight chain products containing one or two functional groups such as carboxyl, aldehyde, hydroxyl, and amino.
      
The urea adduct method avoids hydrogenation and low-temperature crystallization, and furthermore, unsaturated cyclic and unsaturated straight-chain products can be recovered as individual fractions.
      
Terminal alkynes produced straight chain products while internal alkynes produced both terminal and internal products.
      
Furthermore, it was demonstrated that the formation of straight chain products was favoured over branched products.
      
In the absence of added pyridine nucleotides the long chain products of the cleavage reaction are aldehydes.
      
Moreover, their decay chain products generate the bulk of the long-term radiotoxicity of the nuclear waste.
      
Part of the internal triple bond in the alkyne can isomerize to the terminal position and then start chain growth to produce straight chain products.
      
Taken together, these data would seem to demonstrate that peroxisomes are the sole site at which HETEs are metabolized to shorter chain products.
      
The condensation of metal clusters into a variety of infinite chain products, most of which are also centered, is also encountered.
      
The factor Va heavy-chain products a, b, and c appear to be APC associated.
      
The medium and long chain products are degraded more slowly.
      
 

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