SUPPORT THE WORK

GetWiki

Organic synthesis

ARTICLE SUBJECTS
aesthetics  →
being  →
complexity  →
database  →
enterprise  →
ethics  →
fiction  →
history  →
internet  →
knowledge  →
language  →
licensing  →
linux  →
logic  →
method  →
news  →
perception  →
philosophy  →
policy  →
purpose  →
religion  →
science  →
sociology  →
software  →
truth  →
unix  →
wiki  →
ARTICLE TYPES
essay  →
feed  →
help  →
system  →
wiki  →
ARTICLE ORIGINS
critical  →
discussion  →
forked  →
imported  →
original  →
Organic synthesis
[ temporary import ]
please note:
- the content below is remote from Wikipedia
- it has been imported raw for GetWiki
{{about|artificial synthesis of organic compounds|the journal Organic Syntheses|Organic Syntheses|synthesis in organisms|Biosynthesis}}{{refimprove|date=March 2016}}Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds.JOURNAL, Cornforth, JW, 1993-02-01, The Trouble With Synthesis, Australian Journal of Chemistry, 46, 2, 157–170, 10.1071/ch9930157, 2005AJCh...58...69S, Organic molecules are often more complex than inorganic compounds, and their synthesis 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

A total synthesis is the complete chemical synthesis of complex organic molecules from simple, commercially available (petrochemical) or natural precursors.BOOK, Nicolaou, K. C., K. C. Nicolaou, Sorensen, E. J., Classics in Total Synthesis, Wiley-VCH, VCH, 1996, New York, {{page needed|date=March 2016}} 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.JOURNAL, Dighe, Nachiket, 2010, Convergent synthesis: A strategy to synthesize compounds of biological interest,weblink Der Pharmacia Lettre, 2, 318–328, Robert Burns Woodward, who received the 1965 Nobel Prize for Chemistry for several total synthesesWEB,weblink Nobelprize.org, www.nobelprize.org, 2016-11-20, (e.g., his 1954 synthesis of strychnineJOURNAL, Woodward, R. B., M. P., W. D., A., H. U., K., The Total Synthesis of Strychnine, Journal of the American Chemical Society, 76, 18, 4749–4751, 1954, 10.1021/ja01647a088, Cava, Ollis, Hunger, Daeniker, Schenker, ), is regarded as the father of modern organic synthesis. Some latter-day examples include Wender's,JOURNAL, Wender, Paul A., Paul Wender, 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, 10.1021/ja9635387, 0002-7863, Holton's,JOURNAL, 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, 10.1021/ja00083a066, 0002-7863, Nicolaou's,JOURNAL, 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,weblink Nature, en, 367, 6464, 630–634, 10.1038/367630a0, 7906395, 1994Natur.367..630N, and Danishefsky'sJOURNAL, 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, 10.1021/ja952692a, 0002-7863, total syntheses of the anti-cancer therapeutic, paclitaxel (trade name, Taxol).WEB,weblink Taxol – The Drama behind Total Synthesis, www.org-chem.org, 2016-11-20,

Methodology and applications

{{refimprove section|date=March 2016}}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.BOOK, March, J., Smith, D., Advanced Organic Chemistry, 5th ed, John Wiley & Sons, Wiley, 2001, New York, {{page needed|date=March 2016}} 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.JOURNAL, 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., 4, 12, 2337–2347, 10.1039/B602413K, 16763676, 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.JOURNAL, 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,weblink Chemical Society Reviews, en, 41, 15, 10.1039/C2CS35116A, 22743704, 1460-4744, 5185–5238, 3426871, 2012ChSRv..41.6507P, Such applications involve major industries focused especially on polymers (and plastics) and pharmaceuticals.

Stereoselective synthesis

{{refimprove section|date=March 2016}}Most complex natural products are chiral,JOURNAL, Blackmond, Donna G., 2016-11-20, The Origin of Biological Homochirality, Cold Spring Harbor Perspectives in Biology, 2, 5, 10.1101/cshperspect.a002147, 1943-0264, 2857173, 20452962, a002147, BOOK, Advances in Chromatography, Welch, CJ, Marcel Dekker, Inc., 1995, New York, 172, and the bioactivity of chiral molecules varies with the enantiomer.JOURNAL, 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, 1550-9702, 3614593, 23674971, 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 KnowlesJOURNAL, Knowles, William S., 2002-06-17, Asymmetric Hydrogenations (Nobel Lecture),weblink Angewandte Chemie International Edition, en, 41, 12, 1998–2007, 10.1002/1521-3773(20020617)41:123.0.CO;2-8, 1521-3773, 2012AnChe..51.3695M, 2019-02-05, and Ryōji Noyori,JOURNAL, 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, 10.1021/ja00207a038, 1989, and functional group modifications such as the asymmetric epoxidation of Barry Sharpless;JOURNAL, 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, 10.1021/ja00253a032, 0002-7863, for these specific achievements, these workers were awarded the Nobel Prize in Chemistry in 2001.JOURNAL, Service. R.F., 2001, Science Awards Pack a Full House of Winners, Science, print, online science news, 294, 5542; October 19, 503–505, 11641480, 10.1126/science.294.5542.503b,weblink 2 March 2016, 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.BOOK, Corey, E. J., Elias James Corey, Cheng, X-M., The Logic of Chemical Synthesis, John Wiley & Sons, Wiley, 1995, New York, {{page needed|date=March 2016}} 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,{{when|date=March 2016}} and less widely accepted, computer programs have been written for designing a synthesis based on sequences of generic "half-reactions".JOURNAL, Todd, Matthew H., Computer-aided Organic Synthesis, Chemical Society Reviews, 34, 247–266, 2005, 10.1039/b104620a, 15726161, 3,

See also

References

{{Reflist|30em}}

Further reading

  • BOOK, Corey EJ, Elias James Corey, Cheng, X-M, 1995, The Logic of Chemical Synthesis, New York, NY, John Wiley & Sons, 978-0471115946,

External links

{{Commons category|Organic syntheses}} {{chemical synthesis}}{{Organic chemistry}}

- content above as imported from Wikipedia
- "Organic synthesis" does not exist on GetWiki (yet)
- time: 8:04am EST - Mon, Feb 18 2019
[ this remote article is provided by Wikipedia ]
LATEST EDITS [ see all ]
GETWIKI 09 MAY 2016
GETWIKI 18 OCT 2015
M.R.M. Parrott
Biographies
GETWIKI 20 AUG 2014
GETWIKI 19 AUG 2014
GETWIKI 18 AUG 2014
Wikinfo
Culture
CONNECT