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Analytical enantiomer separation of aliphatic diols as boronates and acetals by complexation gas chromatography

✍ Scribed by V. Schurig; D. Wistuba

Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
260 KB
Volume
25
Category
Article
ISSN
0040-4039

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✦ Synopsis

Cgc.&c bohonatecr and acetaes 06 mono-and diaebgk?.bubb~ed 1,2-, 2.3-1,3-.t 1,4-dioL!~ have been quWveRg bepakakd into enatiomm by compkxcction gao chhomatoguphg tizing opkLc&g active metal chekzten. An e~&cient, puk_be f. benbixtive m&hod ~OJL de,WunLning enatiomti p(LtLititi 60% voeatiee gLyco& .& Hun avaieabke. Optically active glycols are useful building blocks in chiral synthesis '. Optically enriched aliphatic diols may also occur as hydrolysis products of the biochemical transformation of race-

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