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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 16, 1986 - Issue 3
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Original Articles

The Use of N-Ethyl-N'-Dimethylamincfropylcarbodiimide or Silicon Tetrachloride in Pyrrole Syntheses

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Pages 357-364 | Published online: 19 Dec 2006

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Benoit Rigo, Dominique Fasseur, Pascal Cauliez & Daniel Couturier. (1989) Disilylated Compounds as Precursors of Heterocycles: A New and Easy Oxadiazole Synthesis. Synthetic Communications 19:13-14, pages 2321-2335.
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Beno[icaron]t Rigo, Dominique Valligny, Sophie Taisne & Daniel Couturier. (1988) Disilylated Compounds as Precursors of Heterocycles : Synthesis of Benzimidazoles, Triazoles, Furan and Pyrrole. Synthetic Communications 18:2, pages 167-180.
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Articles from other publishers (16)

David T. George, Michael J. Williams & Gregory L. Beutner. (2023) Safety as a Factor in Reaction Development: Considerations of Sensitization Potential with Amide Bond Forming Reagents. Helvetica Chimica Acta 106:11.
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Karine Porte, Margaux Riomet, Carlotta Figliola, Davide Audisio & Frédéric Taran. (2020) Click and Bio-Orthogonal Reactions with Mesoionic Compounds. Chemical Reviews 121:12, pages 6718-6743.
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Masami Kawase & Ryosuke Saijo. (2021) The Fascinating Chemistry of Mesoionic 4-Trifluoroacetyl-1,3-oxazolium-5-olates and Related Compounds. HETEROCYCLES 102:9, pages 1643.
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Carlos Aydillo, Nuria Mazo, Claudio D. Navo & Gonzalo Jiménez‐Osés. (2019) Elusive Dehydroalanine Derivatives with Enhanced Reactivity. ChemBioChem 20:10, pages 1246-1250.
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Amanda K. Pearce, Alessandra Travanut, Benoit Couturaud, Vincenzo Taresco, Steven M. Howdle, Morgan R. Alexander & Cameron Alexander. (2017) Versatile Routes to Functional RAFT Chain Transfer Agents through the Passerini Multicomponent Reaction. ACS Macro Letters 6:7, pages 781-785.
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Richard S. Pottorf, Peter Szeto & Madduri Srinivasarao. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis 1 5 .
Hamza Karakuş & Yaşar Dürüst. (2016) Novel benzothiophene 1,1-dioxide deoxygenation path for the microwave-assisted synthesis of substituted benzothiophene-fused pyrrole derivatives. Molecular Diversity 21:1, pages 53-60.
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Sergio Rossi, Maurizio Benaglia & Andrea Genoni. (2014) Organic reactions mediated by tetrachlorosilane. Tetrahedron 70:12, pages 2065-2080.
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Kirsi Harju, Nenad Manevski & Jari Yli-Kauhaluoma. (2009) Microwave-assisted synthesis of pyridylpyrroles from N-acylated amino acids. Tetrahedron 65:47, pages 9702-9706.
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Richard S. Pottorf & Peter Szeto. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Alan R. Katritzky, Tian-Bao Huang, Michael V. Voronkov, Mingyi Wang & Hartmuth Kolb. (2000) Efficient One-Pot Synthesis of Polysubstituted Pyrroles. The Journal of Organic Chemistry 65:25, pages 8819-8821.
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Thierry Granier, Florian Gaiser, Lukas Hintermann & Andrea Vasella. (2004) Synthesis via a Carbohydrate‐Derived Münchnone of Pyrrolopyridines (Indolizines) and imidazopyridines, and their evaluation as inhibitors of β‐D‐glucosidases . Helvetica Chimica Acta 80:5, pages 1443-1456.
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Gordon W. Gribble, Frank L. Switzer, John H. Bushweller, John G. Jewett, Jay H. Brown, Jessica L. Dion, C. Hackett Bushweller, Marianne P. Byrn & Charles E. Strouse. (1996) Stereodynamics of 9,11-Diphenyl-10-azatetracyclo[6.3.0.0. 4,11 0. 5,9 ]undecanes. Highly Restricted Nitrogen Inversion and Isolated Phenyl Rotation. X-ray Crystallographic, Dynamic NMR, and Molecular Mechanics Studies . The Journal of Organic Chemistry 61:13, pages 4319-4327.
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Laurent Désaubry, Camille Georges Wermuth & Jean-Jacques Bourguignon. (1995) Synthesis of a conformationally constrained analogue of BW A78U, an anticonvulsant adenine derivative. Tetrahedron Letters 36:24, pages 4249-4252.
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Gerritt P. Bean. 1990. Chemistry of Heterocyclic Compounds. Chemistry of Heterocyclic Compounds 105 294 .
W. K. ANDERSON & A. R. HEIDER. (2016) ChemInform Abstract: The Use of N‐Ethyl‐N′‐dimethylaminopropylcarbodiimide or Silicon Tetrachloride in Pyrrole Syntheses.. Chemischer Informationsdienst 17:32.
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