Glycal Explained

Glycal is a name for cyclic enol ether derivatives of sugars having a double bond between carbon atoms 1 and 2 of the ring. The term "glycal" should not be used for an unsaturated sugar that has a double bond in any position other than between carbon atoms 1 and 2.[1]

History

The first glycal was synthesized by Hermann Emil Fischer and Karl Zach in 1913.[2] They synthesized this 1,2-unsaturated sugar from D-glucose and named their product D-glucal. Fischer believed he had synthesized an aldehyde, and therefore he gave the product a name that suggested this.[3] By the time he discovered his mistake, the name "glycal" was adopted as a general name for all sugars with a double bond between carbon atoms 1 and 2.[4]

Conformation

Glycals can be formed as pyranose (six-membered) or furanose (five-membered) rings, depending on the monosaccharide used as a starting material to synthesize the glycal. Glycals can also be classified as endo-glycals or exo-glycals. A glycal is an endo-glycal when the double bond is within the ring. If the hydroxyl group on carbon 1 has been replaced with another carbon atom, a double bond can also form outside the ring between carbon 1 and this new carbon. In this case, the product is called an exo-glycal.[5] The glycal conformation that has been studied in most depth is that of the pyranose endo-glycal. The favoured conformation of this glycal is the half-chair,[6] a result which has been confirmed by quantum mechanical calculations.[7]

Synthesis

The original Fischer glycal synthesis was the reductive elimination with zinc of a glycosyl halide. This glycosyl halide was formed from a monosaccharide starting material.[8] Some other synthetic routes include:

A general example of each synthetic route is given below (drawn with first discussed synthesis bottom right, moving clockwise):

Reactions and uses

The double bond of a glycal allows many other functional groups to be introduced into a monosaccharide. Like an alkene, a glycal can undergo electrophilic addition across the double bond to add in these new atoms such as halogens, epoxides, and nitrogen. The glycal double bond also allows a deoxy position (carbon in the ring that doesn’t have an oxygen bonded to it) to be easily introduced.[8]

Glycals have many uses in synthetic carbohydrate chemistry. They are commonly used as glycosylation donors, meaning that they can react with other monosaccharides to form a longer chain of monosaccharides called an oligosaccharide.[11]

Glycals can also have interesting applications in studying biological systems, particularly enzymes. D-glucal and radiolabelled D-galactal have been used to selectively bind with amino acids in the active sites of several enzymes. These enzyme-glycal complexes allow these amino acids that are essential for catalysis to be identified and allow for a better understanding of how these enzymes function.[12]

References

See also

Notes and References

  1. http://www.iupac.org/publications/pac/1996/pdf/6810x1919.pdf IUPAC "Nomenclature of Carbohydrates"
  2. Web site: GLYCALS. Extensive, interesting and inexpensive starting materials for building blocks synthesis . 2018-11-30 . https://web.archive.org/web/20090605162326/http://www.glycoteam.com/n1.htm . 2009-06-05 . dead .
  3. Book: Lindhorst, T.K. . Essentials of Carbohydrate Chemistry and Biology . Wiley-VCH . 2007 . 978-3-527-31528-4 .
  4. Book: Fraser-Reid, B.O. . Tatsuta, K. . Thiem, Joachim . Glycoscience: Chemistry and Chemical Biology I - III . Springer . 2001 . 3-540-67764-X .
  5. Taillefumier, C. . Chapleur, Y. . Synthesis and Uses of exo-Glycals . Chemical Reviews . 2004 . 104 . 263–292 . 10.1021/cr030640v . 14719977 . 1 .
  6. Book: Pigman, W.W. . Wolfrom, M.L.. Melville Wolfrom . Tipson, R.S. . Advances in Carbohydrate Chemistry . Academic Press . 1950 . 0-12-007226-2 .
  7. Ernst, C. . Piacenza, M. . Grimme, S. . Klaffke, W. . Epoxidation of C-branched glycals: unexpected stereochemical results and their theoretical rationale . Carbohydrate Research . 2003 . 338 . 231–236 . 10.1016/S0008-6215(02)00406-8 . 12543555 . 3 .
  8. Book: Lindberg, T.J. . Harmata, M. . Wender, P.A. . Strategies and Tactics in Organic Synthesis . Academic Press . 2004 . 0-12-450287-3 .
  9. Calimente, D. . Postema, M.H.D. . Preparation of C-1 Glycals via Olefin Metathesis. A Convergent and Flexible Approach to C-Glycoside Synthesis . The Journal of Organic Chemistry . 1999 . 64 . 1770–1771 . 10.1021/jo982331o . 11674258 . 6 .
  10. Somsk, L. . Carbanionic Reactivity of the Anomeric Center in Carbohydrates . Chemical Reviews . 2001 . 101 . 81–136 . 10.1021/cr980007n. 11712195 . 1.
  11. Danishefsky, S.J. . McClure, K.F. . Randolf, J.T. . Ruggeri, R.B. . A Strategy for the Solid-Phase Synthesis of Oligosaccharides . Science . 1993 . 260 . 1307–1309 . 10.1126/science.8493573 . 8493573 . 5112 . 1993Sci...260.1307D .
  12. Book: Sigman, D.S. . Mechanisms of Catalysis . Academic Press . 1992 . 0-12-122720-0 .