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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 41, 2011 - Issue 24
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Original Articles

Solvent-Free One-Pot Synthesis of Spiro[indoline-3,4′(1H′)-pyrano[2,3-c]pyrazol]-2-one Derivatives by Grinding

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Pages 3620-3626 | Received 26 Feb 2008, Published online: 22 Aug 2011

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (3)

Seyedeh F. Hojati, Amirhassan Amiri, Sara Mohamadi & Sara Soleimanian. (2023) MOF-199 as an Efficient Metal Organic Framework Catalyst for the Synthesis of Spiro[Indoline-3,4′-Pyrano[2,3-c]Pyrazole] Derivatives. Polycyclic Aromatic Compounds 43:9, pages 8134-8146.
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S. F. Hojati & S. Mohamadi. (2020) Ultrasound Promoted Green Synthesis of Spiro Indoline-3,4′-pyrano[2,3-c]pyrazoles. Organic Preparations and Procedures International 52:4, pages 304-310.
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S. F. Hojati & H. Raouf. (2016) Ionic Liquid for One-pot Synthesis of Spiro[indoline-3,4′-pyrano[2,3-c]pyrazoles]. Organic Preparations and Procedures International 48:6, pages 474-480.
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Articles from other publishers (19)

A. Surya Kumari, C. Sudhakar & K. Swarupa. (2024) Microwave-Assisted One-Pot Synthesis of Spiro[indole-3,4′-pyrano[2,3-c]pyrazoles] Using Polystyrene-Supported p-Toluenesulfonic Acid as Heterogeneous Catalyst under Solvent-Free Conditions. Russian Journal of Organic Chemistry 59:10, pages 1747-1754.
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Seyedeh Fatemeh Hojati, Fariba Zeidabadi Nezhad & Reyhane Kashki. (2022) The investigation of substituent effect in the structure of copolymer as the protecting cover of magnetic nanocomposite on its catalytic activity. Research on Chemical Intermediates 49:2, pages 603-617.
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Jianming Zhao, Xudong Liu, Yan Zhang & Ying Xue. (2021) Exploring the Effects of Water on the Mechanism of the Catalyst-Free Reaction between Isatin and 3-Methyl-2-pyrazolin-5-one from the Mixed Implicit/Explicit Multiple Types of Water Clusters. The Journal of Physical Chemistry B 126:1, pages 249-261.
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Abhishek Upadhyay & R.K.P. Singh. (2021) An Efficient One Pot Four-Component Synthesis of Spiro[indoline-3,4′-pyrano[2,3-c]pyrazole] Derivatives via Electrochemical Approach. Asian Journal of Chemistry 33:7, pages 1685-1691.
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Atieh Rezvanian, Vahideh Zadsirjan, Pegah Saedi & Majid M. Heravi. (2018) Iodine‐Catalyzed One‐Pot Four‐Component Synthesis of Spiro[indoline‐3,4′‐pyrano‐pyrazole] Derivatives. Journal of Heterocyclic Chemistry 55:12, pages 2772-2780.
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Seyedeh Fatemeh Hojati, Amirhassan Amiri, Sakineh Mohamadi & Nasrin MoeiniEghbali. (2017) Novel organometallic nanomagnetic catalyst for multicomponent synthesis of spiroindoline derivatives. Research on Chemical Intermediates 44:4, pages 2275-2287.
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Jutika Devi, Subarna Jyoti Kalita & Dibakar Chandra Deka. (2018) A Quick Micelle‐Catalyzed One‐Pot Synthesis of Spiro[indoline‐3, 4′‐pyrano[2, 3‐ c ]pyrazoles] in Water at Room Temperature . ChemistrySelect 3:5, pages 1512-1516.
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Sakshi Sharma, Goutam Brahmachari, Rajni Kant & Vivek K. Gupta. (2016) One-pot green synthesis of biologically relevant novel spiro[indolin-2-one-3,4′-pyrano[2,3- c ]pyrazoles] and studies on their spectral and X-ray crystallographic behaviors . Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 72:3, pages 335-343.
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Tetyana L. Pavlovska, Ruslan Gr. Redkin, Victoria V. Lipson & Dmytro V. Atamanuk. (2015) Molecular diversity of spirooxindoles. Synthesis and biological activity. Molecular Diversity 20:1, pages 299-344.
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Goutam Brahmachari. (2016) Design for carbon–carbon bond forming reactions under ambient conditions. RSC Advances 6:69, pages 64676-64725.
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Manouchehr Mamaghani, Roghayeh Hossein Nia, Farhad Shirini, Khalil Tabatabaeian & Mehdi Rassa. (2014) An efficient and eco-friendly synthesis and evaluation of antibactrial activity of pyrano[2,3-c]pyrazole derivatives. Medicinal Chemistry Research 24:5, pages 1916-1926.
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Majid M. Heravi, Elaheh Hashemi & Fereshteh Azimian. (2014) N-Sulfonic acid modified poly(styrene-co-maleic anhydride): an efficient and recyclable solid acid catalyst for the synthesis of a wide range of spiropyrans. Journal of the Iranian Chemical Society 12:4, pages 647-653.
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Wang Liju, Keyume Ablajan & Feng Jun. (2015) Rapid and efficient one-pot synthesis of spiro[indoline-3,4′-pyrano[2, 3-c]pyrazole] derivatives catalyzed by l-proline under ultrasound irradiation. Ultrasonics Sonochemistry 22, pages 113-118.
Crossref
Goutam Brahmachari. 2015. Room Temperature Organic Synthesis. Room Temperature Organic Synthesis 1 73 .
Leonid A. Shemchuk, Dmitry A. Lega, Ruslan Gr. Redkin, Valentin P. Chernykh, Oleg V. Shishkin & Svetlana V. Shishkina. (2014) An efficient, three-component synthesis and molecular structure of derivatives of 2-amino-3-R-6-ethyl-4,6-dihydropyrano[3,2-c][2,1]benzothiazine-5,5-dioxide spirocombined with a 2-oxindole nucleus. Tetrahedron 70:44, pages 8348-8353.
Crossref
Pramod B. Thakur & Harshadas M. Meshram. (2014) “On water” highly atom economical and rapid synthesis of a novel class of 3-hydroxy-2-oxindole scaffolds under a catalyst-free and column chromatography-free protocol at room temperature. RSC Advances 4:12, pages 6019.
Crossref
Jiangxia Yu, Yongbing Zhou, Tianhua Shen, Wengang Mao, Kang Chen & Qingbao Song. (2013) Novel and Efficient One-Pot Synthesis of Spiro[Indoline-3,4′-Pyrano [2,3-c]pyrazole]Derivatives Catalysed by L-Proline in Aqueous Medium. Journal of Chemical Research 37:6, pages 365-368.
Crossref
Ying Liu, Zhongjiao Ren, Weiguo Cao, Jie Chen, Hongmei Deng & Min Shao. (2012) ChemInform Abstract: Solvent‐Free One‐Pot Synthesis of Spiro[indoline‐3,4′(1H′)‐pyrano[2,3‐c]pyrazol]‐2‐one Derivatives by Grinding.. ChemInform 43:18.
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Larry Yet. 2012. 243 279 .

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