Synthesis of 1L-1, 2-Dideoxy-1, 2-epithio-myo-inositol through a 1L-1, 2-Anhydro-3, 4:5, 6-bis-O-(tetraisopropyldisiloxane-1, 3-diyl)-myo-inositol intermediate

Author

Todd Frederick Seiple

Date of Award

8-1994

Degree Type

Thesis

Degree Name

Master of Science

Major

Chemistry

Major Professor

David C. Baker

Committee Members

Fred Schell, Spiro D. Alexandratos

Abstract

This research attempted to develop inositol derivatives that could potentially be used as drugs to inhibit a variety of cellular functions. The main emphasis of this research revolved around the formation of an episulfide myoz-inositol derivative through an epoxide intermediate. Other procedures were carried out for the attempted formation of conduritol B and for a nitrogen analogue of myo-inositol.

Recommended Citation

Seiple, Todd Frederick, "Synthesis of 1L-1, 2-Dideoxy-1, 2-epithio-myo-inositol through a 1L-1, 2-Anhydro-3, 4:5, 6-bis-O-(tetraisopropyldisiloxane-1, 3-diyl)-myo-inositol intermediate. " Master's Thesis, University of Tennessee, 1994.
https://trace.tennessee.edu/utk_gradthes/11691