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AbstractAbstract
[en] The subject of this study is the preparation of 11-cis and 9-cis retinals deuterated at specific positions of the chain with a high deuterium incorporation and a high chemical purity. The reaction of opsin with these compounds gives rhodopsin and isorhodopsin with a deuterium label on the predetermined positions of the chromophore. For the introduction of the deuterium the author has used the conversion of a propargyl alcohol into an ethylenic alcohol by the LiAlH4 reductive method. (Auth./C.F.)
Source
31 Mar 1982; 66 p; Includes Dutch summary; 61 refs.; Proefschrift (Dr.).
Record Type
Miscellaneous
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Thesis/Dissertation
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