The coupling of an olefin with a carbonyl compound in the presence of an acid catalyst is known as the 'Prins reaction' which normally provides a mixture of 1,3-diols, 1,3-dioxanes, and allylic alcohols. In particular, the coupling of a homoallylic alcohol with a carbonyl compound in the presence of an acid catalyst is known as the 'Prins cyclization', which is a powerful synthetic tool for the stereo selective synthesis of tetrahydropyran scaffolds. On the other hand, aza-Prins cyclization of homoallylic amides with carbonyl compounds is one of the most elegant approaches for the synthesis of piperidine derivatives. In the same way, thia-Prins cyclization of homoallylicmercaptans with aldehydes under the influence of an acid catalyst provides the corresponding thiotetrahydropyrans with a high selectivity. Thus, the Prins cyclization has emerged as a powerful method for the stereo selective synthesis of a wide range of heterocycles such as tetrahydropyran, piperidine and thiotetrahydropyran scaffolds. In this book, we used Prins reaction for synthesis of bioactive natural products such as Polyrhacitide A, Dodoneine, Epi-dodoneine, Euschapholide and Tetraketide.
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Dr. Dhanraj O. Biradar is an Assistant Professor at Department of Chemistry, Maharashtra Mahavidyalaya, Nilanga, M.S., India. He did Ph.D. from IICT, Hyderabad, T.S., India. He did his postdoctoral research at Organic Chemistry Division, Masaryk University, Brno, Czech Republic under the supervision of Prof. Kamil Paruch.
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Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 176 pp. Englisch. Bestandsnummer des Verkäufers 9786630420074
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Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The coupling of an olefin with a carbonyl compound in the presence of an acid catalyst is known as the 'Prins reaction' which normally provides a mixture of 1,3-diols, 1,3-dioxanes, and allylic alcohols. In particular, the coupling of a homoallylic alcohol with a carbonyl compound in the presence of an acid catalyst is known as the 'Prins cyclization', which is a powerful synthetic tool for the stereo selective synthesis of tetrahydropyran scaffolds. On the other hand, aza-Prins cyclization of homoallylic amides with carbonyl compounds is one of the most elegant approaches for the synthesis of piperidine derivatives. In the same way, thia-Prins cyclization of homoallylicmercaptans with aldehydes under the influence of an acid catalyst provides the corresponding thiotetrahydropyrans with a high selectivity. Thus, the Prins cyclization has emerged as a powerful method for the stereo selective synthesis of a wide range of heterocycles such as tetrahydropyran, piperidine and thiotetrahydropyran scaffolds. In this book, we used Prins reaction for synthesis of bioactive natural products such as Polyrhacitide A, Dodoneine, Epi-dodoneine, Euschapholide and Tetraketide. Bestandsnummer des Verkäufers 9786630420074
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Taschenbuch. Zustand: Neu. PRINS CYCLIZATION & ITS APPLICATION IN SYNTHESIS OF NATURAL PRODUCTS | Synthesis of Bioactive Natural Products Containing 1,3-Diols | Dhanraj O. Biradae (u. a.) | Taschenbuch | Englisch | 2026 | LAP LAMBERT Academic Publishing | EAN 9786630420074 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. Bestandsnummer des Verkäufers 136761563
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Taschenbuch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The coupling of an olefin with a carbonyl compound in the presence of an acid catalyst is known as the 'Prins reaction' which normally provides a mixture of 1,3-diols, 1,3-dioxanes, and allylic alcohols. In particular, the coupling of a homoallylic alcohol with a carbonyl compound in the presence of an acid catalyst is known as the 'Prins cyclization', which is a powerful synthetic tool for the stereo selective synthesis of tetrahydropyran scaffolds. On the other hand, aza-Prins cyclization of homoallylic amides with carbonyl compounds is one of the most elegant approaches for the synthesis of piperidine derivatives. In the same way, thia-Prins cyclization of homoallylicmercaptans with aldehydes under the influence of an acid catalyst provides the corresponding thiotetrahydropyrans with a high selectivity. Thus, the Prins cyclization has emerged as a powerful method for the stereo selective synthesis of a wide range of heterocycles such as tetrahydropyran, piperidine and thiotetrahydropyran scaffolds. In this book, we used Prins reaction for synthesis of bioactive natural products such as Polyrhacitide A, Dodoneine, Epi-dodoneine, Euschapholide and Tetraketide. 176 pp. Englisch. Bestandsnummer des Verkäufers 9786630420074
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Softcover/Taschenbuch. Zustand: Neu. The coupling of an olefin with a carbonyl compound in the presence of an acid catalyst is known as the 'Prins reaction' which normally provides a mixture of 1,3-diols, 1,3-dioxanes, and allylic alcohols. In particular, the coupling of a homoallylic alcohol with a carbonyl compound in the presence of an acid catalyst is known as the 'Prins cyclization', which is a powerful synthetic tool for the stereo selective synthesis of tetrahydropyran scaffolds. On the other hand, aza-Prins cyclization of homoallylic amides with carbonyl compounds is one of the most elegant approaches for the synthesis of piperidine derivatives. In the same way, thia-Prins cyclization of homoallylicmercaptans with aldehydes under the influence of an acid catalyst provides the corresponding thiotetrahydropyrans with a high selectivity. Thus, the Prins cyclization has emerged as a powerful method for the stereo selective synthesis of a wide range of heterocycles such as tetrahydropyran, piperidine and thiotetrahydropyran scaffolds. In this book, we used Prins reaction for synthesis of bioactive natural products such as Polyrhacitide A, Dodoneine, Epi-dodoneine, Euschapholide and Tetraketide. Sprache: Englisch Gewicht in Gramm: 280. Bestandsnummer des Verkäufers IB-2608380
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