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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 16, 1986 - Issue 13
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Original Articles

One Pot Synthesis of Monosubstituted Isopropylidene Malonates

Xian Huang Department of Chemistry, Hangzhou University, Hangzhou, People's Republic of China
&
Linghong Xie Department of Chemistry, Hangzhou University, Hangzhou, People's Republic of China
Pages 1701-1707 | Published online: 05 Dec 2006

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Nitin B. Darvatkar, Amol R. Deorukhkar, Sachin V. Bhilare & Manikrao M. Salunkhe. (2006) Ionic Liquid–Mediated Knoevenagel Condensation of Meldrum's Acid and Aldehydes. Synthetic Communications 36:20, pages 3043-3051.
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Uday V. Desai, D. M. Pore, R. B. Mane, S. B. Solabannavar & P. P. Wadgaonkar. (2004) One Pot Synthesis of Monoalkylated and Mixed, Dialkylated Meldrum's Acid Derivatives. Synthetic Communications 34:1, pages 25-32.
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Paul F. Vogt, Bruce F. Molino & Albert J. Robichaud. (2001) A REGIOSPECIFIC SYNTHESIS OF 3,3,6-TRIMETHYLINDAN-1-ONE. Synthetic Communications 31:5, pages 679-684.
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György Tóth & KatalinE. Kövér. (1995) Simple, Safe, Large Scale Synthesis of 5-Arylmethyl-2,2-dimethyl-1,3-dioxane-4,6-diones and 3-Arylpropanoic Acids. Synthetic Communications 25:19, pages 3067-3074.
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Xian Huang & Han-Zhong Zhang. (1989) Tandem Reduction-Desulfonylation of α-Alkylidene-β-Keto Sulfones. Synthetic Communications 19:1-2, pages 97-105.
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Zhizhen Huang, Linghong Xie & Xian Huang. (1988) Convenient Synthesis and Facile Cleavage of Phenacyl Esters. Synthetic Communications 18:10, pages 1167-1170.
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Articles from other publishers (20)

Syed Nasir Abbas Bukhari, Mohamed Abdelwahab Abdelgawad, Naveed Ahmed, Muhammad Wahab Amjad, Muhammad Ajaz Hussain, Mervat A. Elsherif, Hasan Ejaz, Nasser H. Alotaibi, Ignjat Filipović & Nenad Janković. (2023) Synthesis, Characterization, and Biological Evaluation of Meldrum’s Acid Derivatives: Dual Activity and Molecular Docking Study. Pharmaceuticals 16:2, pages 281.
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Konstantin L. Ivanov, Mikhail Ya. Melnikov & Ekaterina M. Budynina. (2020) Reductive Knoevenagel Condensation with the Zn–AcOH System. Synthesis 53:07, pages 1285-1291.
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Elham Moosazadeh, Enayatollah Sheikhhosseini, Dadkhoda Ghazanfari & Shahla Soltaninejad. (2019) Uncatalyzed Synthesis of New Antibacterial Bisarylidene Meldrum's Acid Derivatives Functionalized with Ether Groups. Letters in Organic Chemistry 16:10, pages 818-824.
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Nenad Janković, Jovana Muškinja, Zoran Ratković, Zorica Bugarčić, Branislav Ranković, Marijana Kosanić & Srđan Stefanović. (2016) Solvent-free synthesis of novel vanillidene derivatives of Meldrum's acid: biological evaluation, DNA and BSA binding study. RSC Advances 6:45, pages 39452-39459.
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G. Thirupathi, M. Venkatanarayana, P. K. Dubey & Y. Bharathi Kumari. (2013) Eco-friendly synthesis and antimicrobial activities of substituted-5-(1H-indol-3-yl)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione derivatives. Medicinal Chemistry Research 23:3, pages 1569-1580.
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G. Thirupathi, M. Venkatanarayana, P. K. Dubey & Y. Bharathi Kumari. (2012) L-Tyrosine as an Eco-Friendly and Efficient Catalyst for Knoevenagel Condensation of Arylaldehydes with Meldrum’s Acid in Solvent-Free Condition under Grindstone Method. Organic Chemistry International 2012, pages 1-4.
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Zvi RappoportAkihiro Nomoto & Akiya Ogawa. 2010. Patai's Chemistry of Functional Groups. Patai's Chemistry of Functional Groups.
Jitender M. Khurana & Kanika Vij. (2011) Nickel nanoparticles catalyzed chemoselective Knoevenagel condensation of Meldrum’s acid and tandem enol lactonizations via cascade cyclization sequence. Tetrahedron Letters 52:28, pages 3666-3669.
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Kazuaki Shimada, Akiko Moro-oka, Akiko Maruyama, Hiroyuki Fujisawa, Toshio Saito, Ryo Kawamura, Hisashi Kogawa, Maiko Sakuraba, Yukichi Takata, Shigenobu Aoyagi, Yuji Takikawa & Chizuko Kabuto. (2007) Synthesis of Isochalcogenazole Rings by Treating β-( N , N -Dimethylcarbamoylchalcogenenyl)alkenyl Ketones with Hydroxylamine- O -sulfonic Acid . Bulletin of the Chemical Society of Japan 80:3, pages 567-577.
Crossref
Nicola Petragnani & Hélio A. Stefani. 2007. Tellurium in Organic Synthesis. Tellurium in Organic Synthesis 115 284 .
Madhukar S. Chande & Rahul R. Khanwelkar. (2005) Michael addition approach for the synthesis of novel spiro compounds and 2-substituted malonic acid derivatives from Meldrum’s acid. Tetrahedron Letters 46:45, pages 7787-7792.
Crossref
Eric Fillion, Dan Fishlock, Ashraf Wilsily & Julie M. Goll. (2005) Meldrum's Acids as Acylating Agents in the Catalytic Intramolecular Friedel−Crafts Reaction. The Journal of Organic Chemistry 70:4, pages 1316-1327.
Crossref
Bunda Hin, Pavel Majer & Takashi Tsukamoto. (2002) Facile Synthesis of α-Substituted Acrylate Esters. The Journal of Organic Chemistry 67:21, pages 7365-7368.
Crossref
Donald C. Dittmer. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Barry M. Trost, Marco A. Ceschi & Burkhard König. (2003) Palladium‐Catalyzed Additions of Alkenyl Epoxides to Pronucleophiles: A Synthesis of the Macrolactam Aglycone of Fluviricin B1. Angewandte Chemie International Edition in English 36:13-14, pages 1486-1489.
Crossref
Barry M. Trost, Marco A. Ceschi & Burkhard König. (2006) Palladiumkatalysierte Addition von Alkenylepoxiden an Pronucleophile: eine Synthese des Makrolactam‐Aglycons von Fluviricin B1. Angewandte Chemie 109:13-14, pages 1562-1564.
Crossref
Nicola Petragnani. 1995. Comprehensive Organometallic Chemistry II. Comprehensive Organometallic Chemistry II 571 601 .
Martin Eberle & Richard G. Lawton. (1988) Thioalkylation ofMeldrum's Acid: Protected alkylidene derivatives of isopropylidene malonate. Helvetica Chimica Acta 71:8, pages 1974-1982.
Crossref
M. Prat, M. Moreno-Mañas & J. Ribas. (1988) Palladium catalyzed c-allylation of highly acidic carbo and heterocyclic β-dicarbonyl compounds. Tetrahedron 44:23, pages 7205-7212.
Crossref
X. HUANG & L. XIE. (2016) ChemInform Abstract: One‐Pot Synthesis of Monosubstituted Isopropylidene Malonates.. ChemInform 18:18.
Crossref

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