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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 30, 2000 - Issue 22
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Original Articles

Synthesis of Pyrimidine-Annelated Heterocycles: Regioselective Synthesis of 1,3,6-Trialkyl Thieno[3,2-d]-Pyrimidine-2,4-Diones

K. C. Majumdar Department of Chemistry, University of Kalyani, Kalyani, 741 235, India
&
N. K. Jana Department of Chemistry, University of Kalyani, Kalyani, 741 235, India
Pages 4183-4196 | Received 17 Nov 1999, Published online: 04 Dec 2007

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Firouz Matloubi Moghaddam, Hassan Zali Boeini & Dordaneh Zargarani. (2005) Solvent-free synthesis of tri-substituted thiophenes via thio-Claisen rearrangement under microwave irradiation: A convenient route to novel tertiary 2-thienyl amines. Journal of Sulfur Chemistry 26:4-5, pages 331-335.
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K. C. Majumdar, N. K. Jana, A. Bandyopadhyay & S. K. Ghosh. (2001) SYNTHESIS OF PYRIMIDINE-ANNELATED HETEROCYCLES: THERMAL REARRANGEMENT OF 1,3-DIMETHYL-5-(PROP-2-ENYLTHIO)-PYRIMIDINE-2,4-DIONES. Synthetic Communications 31:19, pages 2979-2985.
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Articles from other publishers (6)

Lei Zhang, Kun Wan, Huanhuan Wang, Mengyao Wang, Ao Cui, Xin Huang & Bo Peng. (2024) Synthesis of benzothiophenes via sulfonium-[3,3]-rearrangement of aryl sulfoxides with allenenitriles . Organic Chemistry Frontiers 11:8, pages 2208-2214.
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Biswanath DindaBiswanath Dinda. 2017. Essentials of Pericyclic and Photochemical Reactions. Essentials of Pericyclic and Photochemical Reactions 107 160 .
V.P. Litvinov. 2006. 83 143 .
Krishna C. Majumdar, Subhojit Ghosh & Manish Ghosh. (2003) The thio-Claisen rearrangement 1980–2001. Tetrahedron 59:37, pages 7251-7271.
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K.C Majumdar & T Bhattacharyya. (2001) Studies of bioactive heterocycles: amino Claisen rearrangement of 4-N-(4-aryloxybut-2-ynyl),N-methylaminocoumarins. Tetrahedron Letters 42:25, pages 4231-4233.
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K. C. Majumdar & N. K. Jana. (2010) ChemInform Abstract: Synthesis of Pyrimidine‐Anellated Heterocycles: Regioselective Synthesis of 1,3,6‐Trialkylthieno[3,2‐d]pyrimidine‐2,4‐diones.. ChemInform 32:3.
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