Organic synthesis

This article is about artificial synthesis of organic compounds. For the journal Organic Syntheses, see Organic Syntheses. For synthesis in organisms, see Biosynthesis.

Organic synthesis is a special branch of chemical synthesis and is concerned with the construction of organic compounds via organic reactions. Organic molecules often contain a higher level of complexity than purely inorganic compounds, so that the synthesis of organic compounds has developed into one of the most important branches of organic chemistry. There are several main areas of research within the general area of organic synthesis: total synthesis, semisynthesis, and methodology.

Total synthesis

Main article: Total synthesis

A total synthesis is the complete chemical synthesis of complex organic molecules from simple, commercially available (petrochemical) or natural precursors.[1] Total synthesis may be accomplished either via a linear or convergent approach. In a linear synthesis—often adequate for simple structures—several steps are performed one after another until the molecule is complete; the chemical compounds made in each step are called synthetic intermediates. For more complex molecules, a convergent synthetic approach may be preferable, one that involves individual preparation of several "pieces" (key intermediates), which are then combined to form the desired product.[2]

Robert Burns Woodward, who received the 1965 Nobel Prize for Chemistry for several total syntheses[3] (e.g., his 1954 synthesis of strychnine[4]), is regarded as the father of modern organic synthesis. Some latter-day examples include Wender's,[5] Holton's,[6] Nicolaou's,[7] and Danishefsky's[8] total syntheses of the anti-cancer therapeutic, paclitaxel (trade name, Taxol).[9]

Methodology and applications

Each step of a synthesis involves a chemical reaction, and reagents and conditions for each of these reactions must be designed to give an adequate yield of pure product, with as little work as possible.[10] A method may already exist in the literature for making one of the early synthetic intermediates, and this method will usually be used rather than an effort to "reinvent the wheel". However, most intermediates are compounds that have never been made before, and these will normally be made using general methods developed by methodology researchers. To be useful, these methods need to give high yields, and to be reliable for a broad range of substrates. For practical applications, additional hurdles include industrial standards of safety and purity.[11]

Methodology research usually involves three main stages: discovery, optimisation, and studies of scope and limitations. The discovery requires extensive knowledge of and experience with chemical reactivities of appropriate reagents. Optimisation is a process in which one or two starting compounds are tested in the reaction under a wide variety of conditions of temperature, solvent, reaction time, etc., until the optimum conditions for product yield and purity are found. Finally, the researcher tries to extend the method to a broad range of different starting materials, to find the scope and limitations. Total syntheses (see above) are sometimes used to showcase the new methodology and demonstrate its value in a real-world application.[12] Such applications involve major industries focused especially on polymers (and plastics) and pharmaceuticals.

Stereoselective synthesis

Main article: Chiral synthesis

Most complex natural products are chiral,[13][14] and the bioactivity of chiral molecules varies with the enantiomer.[15] Historically, total syntheses targeted racemic mixtures, mixtures of both possible enantiomers, after which the racemic mixture might then be separated via chiral resolution.

In the later half of the twentieth century, chemists began to develop methods of stereoselective catalysis and kinetic resolution whereby reactions could be directed to produce only one enantiomer rather than a racemic mixture. Early examples include stereoselective hydrogenations (e.g., as reported by William Knowles[16] and Ryōji Noyori[17]), and functional group modifications such as the asymmetric epoxidation of Barry Sharpless;[18] for these specific achievements, these workers were awarded the Nobel Prize in Chemistry in 2001.[19] Such reactions gave chemists a much wider choice of enantiomerically pure molecules to start from, where previously only natural starting materials could be used. Using techniques pioneered by Robert B. Woodward and new developments in synthetic methodology, chemists became more able to take simple molecules through to more complex molecules without unwanted racemisation, by understanding stereocontrol, allowing final target molecules to be synthesised pure enantiomers (i.e., without need for resolution). Such techniques are referred to as stereoselective synthesis.

Synthesis design

Elias James Corey brought a more formal approach to synthesis design, based on retrosynthetic analysis, for which he won the Nobel Prize for Chemistry in 1990. In this approach, the synthesis is planned backwards from the product, using standard rules.[20] The steps "breaking down" the parent structure into achievable component parts are shown in a graphical scheme that uses retrosynthetic arrows (drawn as ⇒, which in effect, mean "is made from").

More recently, and less widely accepted, computer programs have been written for designing a synthesis based on sequences of generic "half-reactions".[21]

See also

Publications

Specialized methods

References

  1. ↑ Nicolaou, K. C.; Sorensen, E. J. (1996). Classics in Total Synthesis. New York: VCH.
  2. ↑ Dighe, Nachiket (2010). "Convergent synthesis: A strategy to synthesize compounds of biological interest" (PDF). Der Pharmacia Lettre. 2: 318–328.
  3. ↑ "Nobelprize.org". www.nobelprize.org. Retrieved 2016-11-20.
  4. ↑ Woodward, R. B.; Cava, M. P.; Ollis, W. D.; Hunger, A.; Daeniker, H. U.; Schenker, K. (1954). "The Total Synthesis of Strychnine". Journal of the American Chemical Society. 76 (18): 4749–4751. doi:10.1021/ja01647a088.
  5. ↑ Wender, Paul A.; Badham, Neil F.; Conway, Simon P.; Floreancig, Paul E.; Glass, Timothy E.; Gränicher, Christian; Houze, Jonathan B.; Jänichen, Jan; Lee, Daesung (1997-03-01). "The Pinene Path to Taxanes. 5. Stereocontrolled Synthesis of a Versatile Taxane Precursor". Journal of the American Chemical Society. 119 (11): 2755–2756. doi:10.1021/ja9635387. ISSN 0002-7863.
  6. ↑ Holton, Robert A.; Somoza, Carmen; Kim, Hyeong Baik; Liang, Feng; Biediger, Ronald J.; Boatman, P. Douglas; Shindo, Mitsuru; Smith, Chase C.; Kim, Soekchan (1994-02-01). "First total synthesis of taxol. 1. Functionalization of the B ring". Journal of the American Chemical Society. 116 (4): 1597–1598. doi:10.1021/ja00083a066. ISSN 0002-7863.
  7. ↑ Nicolaou, K. C.; Yang, Z.; Liu, J. J.; Ueno, H.; Nantermet, P. G.; Guy, R. K.; Claiborne, C. F.; Renaud, J.; Couladouros, E. A. (1994-02-17). "Total synthesis of taxol". Nature. 367 (6464): 630–634. doi:10.1038/367630a0.
  8. ↑ Danishefsky, Samuel J.; Masters, John J.; Young, Wendy B.; Link, J. T.; Snyder, Lawrence B.; Magee, Thomas V.; Jung, David K.; Isaacs, Richard C. A.; Bornmann, William G. (1996-01-01). "Total Synthesis of Baccatin III and Taxol". Journal of the American Chemical Society. 118 (12): 2843–2859. doi:10.1021/ja952692a. ISSN 0002-7863.
  9. ↑ "Taxol – The Drama behind Total Synthesis". www.org-chem.org. Retrieved 2016-11-20.
  10. ↑ March, J.; Smith, D. (2001). Advanced Organic Chemistry, 5th ed. New York: Wiley.
  11. ↑ Carey, J.S.; Laffan, D.; Thomson, C. & Williams, M.T. (2006). "Analysis of the reactions used for the preparation of drug candidate molecules". Org. Biomol. Chem. (print, online research report). 4: 2337–2347. doi:10.1039/B602413K.
  12. ↑ Nicolaou, K. C.; Hale, Christopher R. H.; Nilewski, Christian; Ioannidou, Heraklidia A. (2012-07-09). "Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance". Chemical Society Reviews. 41 (15). doi:10.1039/C2CS35116A. ISSN 1460-4744.
  13. ↑ Blackmond, Donna G. (2016-11-20). "The Origin of Biological Homochirality". Cold Spring Harbor Perspectives in Biology. 2 (5). doi:10.1101/cshperspect.a002147. ISSN 1943-0264. PMC 2857173Freely accessible. PMID 20452962.
  14. ↑ Welch, CJ (1995). Advances in Chromatography. New York: Marcel Dekker, Inc. p. 172.
  15. ↑ Nguyen, Lien Ai; He, Hua; Pham-Huy, Chuong (2016-11-20). "Chiral Drugs: An Overview". International Journal of Biomedical Science : IJBS. 2 (2): 85–100. ISSN 1550-9702. PMC 3614593Freely accessible. PMID 23674971.
  16. ↑ Knowles, William S. (2002-06-17). "Asymmetric Hydrogenations (Nobel Lecture)". Angewandte Chemie International Edition. 41 (12): 1998–2007. doi:10.1002/1521-3773(20020617)41:123.0.CO;2-8. ISSN 1521-3773.
  17. ↑ Noyori, R.; Ikeda, T.; Ohkuma, T.; Widhalm, M.; Kitamura, M.; Takaya, H.; Akutagawa, S.; Sayo, N.; Saito, T. "Stereoselective hydrogenation via dynamic kinetic resolution". Journal of the American Chemical Society. 111 (25): 9134–9135. doi:10.1021/ja00207a038.
  18. ↑ Gao, Yun; Klunder, Janice M.; Hanson, Robert M.; Masamune, Hiroko; Ko, Soo Y.; Sharpless, K. Barry (1987-09-01). "Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization". Journal of the American Chemical Society. 109 (19): 5765–5780. doi:10.1021/ja00253a032. ISSN 0002-7863.
  19. ↑ Service. R.F. (2001). "Science Awards Pack a Full House of Winners" (print, online science news). Science. 294 (5542; October 19): 503–505. doi:10.1126/science.294.5542.503b. PMID 11641480. Retrieved 2 March 2016.
  20. ↑ Corey, E. J.; Cheng, X-M. (1995). The Logic of Chemical Synthesis. New York: Wiley.
  21. ↑ Todd, Matthew H. (2005). "Computer-aided Organic Synthesis". Chemical Society Reviews. 34 (3): 247–266. doi:10.1039/b104620a. PMID 15726161.
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