Aldol condensation

Definition: An aldol addition where an enol or enolate reacts with a carbonyl compound to form an alpha,beta-unsaturated ketone.

ID: RXNO:0000017

More about the RSC Name Reaction Ontology (RXNO)

Articles referencing this term

Copper nanoparticles on hydrotalcite as a heterogeneous catalyst for oxidant-free dehydrogenation of alcohols
Takato Mitsudome, Yusuke Mikami, Kaori Ebata, Tomoo Mizugaki, Koichiro Jitsukawa and Kiyotomi Kaneda, Chem. Commun., 2008 , 4804
DOI: 10.1039/b809012b

A thermal 6π electrocyclization strategy towards taiwaniaquinoids. First enantiospecific synthesis of (−)-taiwaniaquinone G
Enrique Alvarez-Manzaneda, Rachid Chahboun, Eduardo Cabrera, Esteban Alvarez, Ali Haidour, Jose Miguel Ramos, Ramón Alvarez-Manzaneda, Mohammed Hmamouchi and Hakima Es-Samti, Chem. Commun., 2009 , 592
DOI: 10.1039/b816812a

Asymmetric catalysis with chiral primary amine-based organocatalysts
Li-Wen Xu, Jie Luo and Yixin Lu, Chem. Commun., 2009 , 1807
DOI: 10.1039/b821070e

Synthesis and structure of air-stable Lewis acidic binuclear complex of zirconocene pentafluorophenylsulfonate and its catalytic application in the allylation of carbonyl compounds with tetraallyltin
Renhua Qiu, Xinhua Xu, Yinhui Li, Guoping Zhang, Lingling Shao, Delie An and Shuangfeng Yin, Chem. Commun., 2009 , 1679
DOI: 10.1039/b821366f

A heterogeneous Ru/CeO₂ catalyst effective for transfer-allylation from homoallyl alcohols to aldehydes
Hiroki Miura, Kenji Wada, Saburo Hosokawa, Masahiro Sai, Teruyuki Kondo and Masashi Inoue, Chem. Commun., 2009 , 4112
DOI: 10.1039/b901830a

A critical look at reactions in class I and II gas-expanded liquids using CO₂ and other gases
Geoffrey R. Akien and Martyn Poliakoff, Green Chem., 2009 , 11 , 1083
DOI: 10.1039/b904097h

Cycloabiesesquine A, a unique sesquiterpenoid from Abies delavayi
Xian-Wen Yang, Yuanqing Ding, Xing-Cong Li, Daneel Ferreira, Yun-Heng Shen, Su-Mei Li, Ning Wang and Wei-Dong Zhang, Chem. Commun., 2009 , 3771
DOI: 10.1039/b905710b

Recent extensions of the Morita–Baylis–Hillman reaction
Guang-Ning Ma, Jia-Jun Jiang, Min Shi and Yin Wei, Chem. Commun., 2009 , 5496
DOI: 10.1039/b909405a

Hydrodeoxygenation and coupling of aqueous phenolics over bifunctional zeolite-supported metal catalysts
Do-Young Hong, Stephen J. Miller, Pradeep K. Agrawal and Christopher W. Jones, Chem. Commun., 2010 , 46 , 1038
DOI: 10.1039/b918209h

Total synthesis of (±)-Vertine with Z-selective RCM as a key step
Laetitia Chausset-Boissarie, Roman Àrvai, Graham R. Cumming, Céline Besnard and E. Peter Kündig, Chem. Commun., 2010 , 46 , 6264
DOI: 10.1039/c0cc01885f

Green alcohol couplings without transition metal catalysts: base-mediated β-alkylation of alcohols in aerobic conditions
Laura J. Allen and Robert H. Crabtree, Green Chem., 2010 , 12 , 1362
DOI: 10.1039/c0gc00079e

Organosilicon-mediated total synthesis of the triquinane sesquiterpenes (±)-β-isocomene and (±)-isocomene
Arndt W. Schmidt, Thomas Olpp, Elke Baum, Tina Stiffel and Hans-Joachim Knölker, Org. Biomol. Chem., 2010 , 8 , 4562
DOI: 10.1039/c0ob00051e

Synthesis of 1,2-annulated and 1,2-unsubstituted pyrrolo[2,1,5-de]quinolizin-5-ones (cycl[3.3.2]azin-5-ones) via [3+2] cycloadditions of 1-oxoquinolizinium ylides with cyclic alkenes
Yun Liu, Hua-You Hu, Yan Zhang, Hong-Wen Hu and Jian-Hua Xu, Org. Biomol. Chem., 2010 , 8 , 4921
DOI: 10.1039/c0ob00299b

Synthesis enables a structural revision of the Mycobacterium tuberculosis-produced diterpene, edaxadiene
Jillian E. Spangler, Cheryl A. Carson and Erik J. Sorensen, Chem. Sci., 2010 , 1 , 202
DOI: 10.1039/c0sc00284d

Synthesis and biological evaluation of novel semi-conservative monocarbonyl analogs of curcumin as anti-inflammatory agents
Zhe Wang, Peng Zou, Chenglong Li, Wenfei He, Bing Xiao, Qilu Fang, Wenbo Chen, Suqing Zheng, Yunjie Zhao, Yuepiao Cai and Guang Liang, Med. Chem. Commun., 2015 , 6 , 1328
DOI: 10.1039/c5md00114e

Synthesis, biological evaluation and mechanism study of a class of benzylideneindanone derivatives as novel anticancer agents
Jinhui Hu, Jun Yan, Jie Chen, Yanqing Pang, Ling Huang and Xingshu Li, Med. Chem. Commun., 2015 , 6 , 1318
DOI: 10.1039/c5md00139k