Books on the topic 'Heterocycle'

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1

Kaur, Navjeet. Lawesson’s Reagent in Heterocycle Synthesis. Singapore: Springer Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-4655-3.

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2

Petrone, David A. Stereoselective Heterocycle Synthesis via Alkene Difunctionalization. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-77507-4.

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3

Wang, Yinli. Development of a New Heterocycle-Forming Reaction and Kinetic Resolution with N-Heterocyclic Carbenes. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9398-3.

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4

Wu, Xiao-Feng, ed. Transition Metal-Catalyzed Heterocycle Synthesis via CH Activation. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527691920.

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5

R, Katritzky Alan, Soldatenkov, A. T. (Anatoliĭ Timofeevich), and ebrary Inc, eds. Heterocycles in life and society: An introduction to heterocyclic chemistry, biochemistry and applications. 2nd ed. Chichester, West Sussex: Wiley, 2011.

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6

Pozharskiĭ, A. F. Heterocycles in life and society: An introduction to heterocyclic chemistry and biochemistry and the role of heterocycles in science, technology, medicine, and agriculture. Chichester: Wiley, 1997.

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7

Ameta, Keshav Lalit, Ravi Kant, Andrea Penoni, Angelo Maspero, and Luca Scapinello, eds. N-Heterocycles. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0832-3.

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8

Iskra, Jernej, ed. Halogenated Heterocycles. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25103-0.

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9

Gakh, Andrei A., and Kenneth L. Kirk, eds. Fluorinated Heterocycles. Washington, DC: American Chemical Society, 2009. http://dx.doi.org/10.1021/bk-2009-1003.

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10

Gakh, Andrei A. Fluorinated heterocycles. Edited by American Chemical Society. Division of Fluorine Chemistry and American Chemical Society Meeting. Washington, DC: American Chemical Society, 2009.

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11

Phosphorous heterocycles. Dordrecht: Springer, 2009.

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12

Eguchi, Shoji. Bioactive heterocycles. Edited by Eguchi Shoji. Berlin: Springer, 2006.

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13

Motohashi, Noboru, ed. Bioactive Heterocycles VI. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-79218-5.

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14

Khan, Mahmud Tareq Hassan, ed. Bioactive Heterocycles III. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-73402-4.

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15

Khan, Mahmud Tareq Hassan, ed. Bioactive Heterocycles IV. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-73404-8.

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16

Khan, Mahmud Tareq Hassan, ed. Bioactive Heterocycles V. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-73406-2.

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17

Motohashi, Noboru, ed. Bioactive Heterocycles VII. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-00336-3.

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18

Bansal, Raj K., ed. Phosphorous Heterocycles I. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-00338-7.

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19

Somsák, László, ed. Carbohydrate-spiro-heterocycles. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-31942-7.

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20

Eguchi, Shoji, ed. Bioactive Heterocycles I. Berlin/Heidelberg: Springer-Verlag, 2006. http://dx.doi.org/10.1007/11514725.

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21

Diana, Patrizia, and Girolamo Cirrincione. Biosynthesis of Heterocycles. Hoboken, NJ, USA: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118960554.

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22

Eguchi, Shoji, ed. Bioactive Heterocycles II. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-72592-3.

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23

Bansal, Raj K., ed. Phosphorus Heterocycles II. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-12254-5.

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24

Khan, Mahmud Tareq Hassan. Bioactive Heterocycles III. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2007.

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25

Kaur, Navjeet. Three-Membered Heterocycle Synthesis. Elsevier, 2024.

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26

Four-Membered Heterocycle Synthesis. Elsevier, 2023.

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27

Kaur, Navjeet. Four-Membered Heterocycle Synthesis. Elsevier, 2023.

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28

Modern Strategies for Heterocycle Synthesis. MDPI, 2021. http://dx.doi.org/10.3390/books978-3-0365-0341-7.

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29

Kaur, Navjeet. Lawesson's Reagent in Heterocycle Synthesis. Springer, 2022.

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30

Kaur, Navjeet. Lawesson's Reagent in Heterocycle Synthesis. Springer Singapore Pte. Limited, 2021.

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31

Kaur, Navjeet. 5-Membered Heterocycle Synthesis Using Iodine. Elsevier, 2022.

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32

Kaur, Navjeet. 5-Membered Heterocycle Synthesis Using Iodine. Elsevier, 2022.

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33

Key Heterocycle Cores for Designing Multitargeting Molecules. Elsevier, 2018. http://dx.doi.org/10.1016/c2016-0-01252-4.

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34

Silakari, Om. Key Heterocycle Cores for Designing Multitargeting Molecules. Elsevier, 2018.

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35

Wang, Yinli. Development of a New Heterocycle-Forming Reaction and Kinetic Resolution with N-Heterocyclic Carbenes. Springer, 2019.

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36

Wang, Yinli. Development of a New Heterocycle-Forming Reaction and Kinetic Resolution with N-Heterocyclic Carbenes. Springer Singapore Pte. Limited, 2020.

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37

Silakari, Om. Key Heterocycle Cores for Designing Multi-Targeting Molecules. Elsevier Science & Technology Books, 2018.

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38

Atta-ur-Rahman, ed. Advances in Organic Synthesis: Volume 17. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/97898150405241221701.

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Abstract:
Advances in Organic Synthesis is a book series devoted to the latest advances in synthetic approaches towards challenging structures. The series presents comprehensive reviews written by eminent authorities on different synthetic approaches to selected target molecules and new methods developed to achieve specific synthetic transformations or optimal product yields. Advances in Organic Synthesis is essential for all organic chemists in academia and the industry who wish to keep abreast of rapid and important developments in the field. Contents of this volume include these 6 reviews: - Multicomponent synthesis of heterocycles by microwave irradiation - Stereoselective procedures for the synthesis of olefines - Advanced microwave assisted organic synthesis method in organic chemistry - Five and six-membered n-heterocycle rings from diaminomaleonitrile - Peptidomimetics: current and future perspectives on hiv protease inhibitors - A review on synthesis, chemistry, and medicinal properties of benzothiazines and their related scaffolds
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39

Wu, Xiao-Feng. Transition Metal-Catalyzed Heterocycle Synthesis Via C-H Activation. Wiley & Sons, Limited, John, 2016.

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40

Wu, Xiao-Feng. Transition Metal-Catalyzed Heterocycle Synthesis Via C-H Activation. Wiley & Sons, Incorporated, John, 2015.

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41

Wu, Xiao-Feng. Transition Metal-Catalyzed Heterocycle Synthesis Via C-H Activation. Wiley & Sons, Incorporated, John, 2015.

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42

Yang, Zhijun. Heterocycle stabilized carbanions: Novel synthon equivalents in organic synthesis. 1994.

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43

Metals and Non-Metals: Five-Membered N-heterocycle Synthesis. Taylor & Francis Group, 2020.

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44

Kaur, Navjeet. Metals and Non-Metals: Five-Membered N-heterocycle Synthesis. Taylor & Francis Group, 2020.

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45

Wu, Xiao-Feng. Transition Metal-Catalyzed Heterocycle Synthesis Via C-H Activation. Wiley-VCH Verlag GmbH, 2016.

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46

Kaur, Navjeet. Metals and Non-Metals: Five-Membered N-heterocycle Synthesis. Taylor & Francis Group, 2020.

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47

Kaur, Navjeet. Metals and Non-Metals: Five-Membered N-heterocycle Synthesis. Taylor & Francis Group, 2020.

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48

Wu, Xiao-Feng. Transition Metal-Catalyzed Heterocycle Synthesis Via C-H Activation. Wiley & Sons, Incorporated, John, 2015.

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49

Wu, Xiao-Feng. Noble Metal Noble Value: Ru-, Rh-, Pd-Catalyzed Heterocycle Synthesis. Imperial College Press, 2016.

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50

Wu, Xiao-Feng, and Yahui Li. Transition Metal-Catalyzed Benzofuran Synthesis: Transition Metal-Catalyzed Heterocycle Synthesis Series. Elsevier Science & Technology Books, 2017.

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