Exploratory study of β-carotene autoxidation
✍ Scribed by Raphael C. Mordi; John C. Walton; Graham W. Burton; Lise Hughes; Keith U. Ingold; David A. Lindsay
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 228 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
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The synthesis of 10,lO' 19,19 , 19,19' , 19' 19'-2H8p-carotene is described. The double condensation (C15+C o+C15=C40) of the Wittig salt of 9 , 9 , 9 , 10-2H4-pionyliaene ethanol with the symmetrical Cl0 dial 2,7- dimethyl-2 , 4 , 6-octatrienedial led directly to 2H -pcarotene. The symmetrical labe
In response to a need for relative large amounts of highly labeled 14C p carotene, a search was made for a biological system which would supply an adequate amount of carotene with sufficient label. Methods previously described did not appear to be adequate appear to devote a greater part of their me