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A team of chemists led by Young Lok Choi and Jung-Nyoung Heo successfully synthesized dibenzoheptenones by combining a suzuki-miyaura coupling reaction with an aldol condensation reaction.<ref>{{Cite journal|last=Kim|first=Joa|last2=Kim|first2=Young|last3=Jung-Nyoung|first3=Heo|date=Winter 2017|title=Total Synthesis of Aristolactams via a One-Pot Suzuki−Miyaura Coupling/Aldol Condensation Cascade Reaction|url=http://pubs.acs.org/doi/abs/10.1021/ol801291k|journal=Journal of Organic Letters|volume=10|pages=3543-3546|via=}}</ref> These dibenzoheptenone form the skeleton for important medicinal drugs such as colchicine (anti-inflamatory used to treat gout). A team of chemists led by Young Lok Choi and Jung-Nyoung Heo successfully synthesized dibenzoheptenones by combining a suzuki-miyaura coupling reaction with an aldol condensation reaction.<ref>{{Cite journal|last=Kim|first=Joa|last2=Kim|first2=Young|last3=Jung-Nyoung|first3=Heo|date=Winter 2017|title=Total Synthesis of Aristolactams via a One-Pot Suzuki−Miyaura Coupling/Aldol Condensation Cascade Reaction|url=http://pubs.acs.org/doi/abs/10.1021/ol801291k|journal=Journal of Organic Letters|volume=10|pages=3543-3546|via=}}</ref> These dibenzoheptenone form the skeleton for important medicinal drugs such as colchicine (anti-inflamatory used to treat gout).


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Condensation reactions have also recently been used to initiate tandem C-N bond formation to form heterocycles. In a paper published in 2017 by a team led by  Yan-Xiao Jiao and Gui-Fa Su* they managed to form quinoxilines which is a structure that is used throughout the pharmaceutical and technological industry.<ref>{{Cite journal|last=Jiao|first=Yan-Xiao|last2=Wu|first2=Ling-Ling|last3=Su|first3=Gui-FA|date=Winter 2017|title=Tandem C–N Bond Formation through Condensation and Metal-Free N-Arylation: Protocol for Synthesizing Diverse Functionalized Quinoxalines|url=http://pubs.acs.org/doi/abs/10.1021/acs.joc.7b00011|journal=Journal of Organic Chemistry|volume=82|pages=4407-4417|via=}}</ref> Condensation reactions have also recently been used to initiate tandem C-N bond formation to form heterocycles. In a paper published in 2017 by a team led by  Yan-Xiao Jiao and Gui-Fa Su* they managed to form quinoxilines which is a structure that is used throughout the pharmaceutical and technological industry.<ref>{{Cite journal|last=Jiao|first=Yan-Xiao|last2=Wu|first2=Ling-Ling|last3=Su|first3=Gui-FA|date=Winter 2017|title=Tandem C–N Bond Formation through Condensation and Metal-Free N-Arylation: Protocol for Synthesizing Diverse Functionalized Quinoxalines|url=http://pubs.acs.org/doi/abs/10.1021/acs.joc.7b00011|journal=Journal of Organic Chemistry|volume=82|pages=4407-4417|via=}}</ref>


Revision as of 19:58, 28 December 2017

A condensation reaction is a class of an organic addition reaction that proceeds in a step-wise fashion to produce the addition product, usually in equilibrium, and a water molecule (hence the name condensation). The reaction may otherwise involve the formation of ammonia, ethanol, or acetic acid. It is a versatile class of reactions that can occur in acidic or basic conditions or in the presence of a catalyst. This class of reactions is a vital part of life as it is essential to the formation of peptide bonds between amino acids.

This oxidation is an example of a condensation reaction involved in the linking of peptides.

There are also copious variations of condensation reactions carried out in the lab, common examples include the Aldol Condensation, the Claisen Condensation, the Knoevenagel Reaction and the Dieckman Condensation (intramolecular Claisen Condensation).

Condensation reaction between two symmetrical aldehydes. The final product is formed irreversibly due to stability from the conjugation of the double bonds.
  1. "Condensation Reaction". IUPAC Copendium of Chemical Terminology (Gold Book). IUPAC. Retrieved 7 December 2017.
  2. Voet, Donald; Voet, Judith; Pratt, Chriss (2008). Fundamentals of Biochemistry. Hoboken, NJ: John Wiley & Sons, Inc. p. 88. ISBN 978-0470-12930-2.
  3. Bruckner, Reinhard (2002). Advanced Organic Chemistry (First ed.). San Diego, California: Harcourt Academic Press. p. 414. ISBN 0-12-138110-2.

Mechanistic Details

The numerous variations of condensation reactions which correspond to numerous mechanisms. In many condensation reactions there is a carbonyl which acts as an electrophile and either another carbonyl that can enolize or

Knoevenagel Reaction Mechanism

This reaction takes between a carbonyl compound and a activated methylene compound or with a nitromethane group, in mildly basic conditions. The final product of the reaction is an alkene with two geminal acceptor groups or one nitro group.

Mechanism for the reaction of active-methylene compounds with carbonyls to form alkenes.
Mechanism for the reaction of active-methylene compounds with carbonyls to form alkenes.

Crossed Claisen Condensation Reaction Mechanism

The crossed claisen reaction results in the acylation of an ester enolate with another ester. These reactions are only possible when one ester has no alpha hydrogens. The reaction conditions call for a highly basic solution and a rapid acidic workup to achieve the final compound.

Formation of diethyl phenylmalonte by a crossed claisen condensation reaction.
Formation of diethyl phenylmalonte by a crossed claisen condensation reaction.

Modern Synthetic Applications

Condensation reactions are used throughout the field of synthetic and medicinal chemistry to synthesize target compounds. Their familiarity and predictable nature make them a widely used synthetic tool. In this section are several examples of some recent uses of condensation reactions in the fields of medicinal and synthetic chemistry.

A team of chemists led by Young Lok Choi and Jung-Nyoung Heo successfully synthesized dibenzoheptenones by combining a suzuki-miyaura coupling reaction with an aldol condensation reaction. These dibenzoheptenone form the skeleton for important medicinal drugs such as colchicine (anti-inflamatory used to treat gout).

Condensation reactions have also recently been used to initiate tandem C-N bond formation to form heterocycles. In a paper published in 2017 by a team led by  Yan-Xiao Jiao and Gui-Fa Su* they managed to form quinoxilines which is a structure that is used throughout the pharmaceutical and technological industry.

See also

References

  1. Bruckner, Reinhard (2002). Advanced Organic Chemistry. San Diego, California: Harcourt Academic Press. p. 414. ISBN 0-12-138110-2.
  2. Bruckner, Reinhard (2002). Advanced Organic Chemistry. San Diego, California: Harcourt Academic Press. p. 418. ISBN 0-12-138110-2.
  3. Kim, Joa; Kim, Young; Jung-Nyoung, Heo (Winter 2017). "Total Synthesis of Aristolactams via a One-Pot Suzuki−Miyaura Coupling/Aldol Condensation Cascade Reaction". Journal of Organic Letters. 10: 3543–3546.
  4. Jiao, Yan-Xiao; Wu, Ling-Ling; Su, Gui-FA (Winter 2017). "Tandem C–N Bond Formation through Condensation and Metal-Free N-Arylation: Protocol for Synthesizing Diverse Functionalized Quinoxalines". Journal of Organic Chemistry. 82: 4407–4417.
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