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Books on the topic 'Ring formation'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

1954-, Giuliano Robert M., American Chemical Society. Division of Carbohydrate Chemistry., and American Chemical Society Meeting, eds. Cycloaddition reactions in carbohydrate chemistry. American Chemical Society, 1992.

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2

1933-, Tebby John C., ed. Alkynes in cycloadditions. Wiley, 2014.

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3

1930-, Hassner Alfred, ed. Synthesis of heterocycles via cycloadditions II. Springer, 2008.

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4

Valters, Raimonds E. Ring-chain tautomerism. Plenum, 1985.

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5

Appelbe, Ruth. Synthetic applications of cationic arene-alkene cyclisations. University College Dublin, 1997.

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6

Manus, Eileen Mc. Oxazolidine and thiazolidine ring opening reactions. University College Dublin, 1996.

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7

Margetic, Davor. Microwave assisted cycloaddition reactions. Nova Science Publishers, 2012.

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8

Harmata, Michael. Advances in cycloaddition. JAI Press, 1999.

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9

de, Meijere A., ed. Small ring compounds in organic synthesis. Springer-Verlag, 1986.

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10

I, Gevaza I͡U. Ėlektrofilʹnai͡a vnutrimolekuli͡arnai͡a t͡siklizat͡sii͡a olefinov. Nauk. dumka, 1990.

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11

Byrne, Maeve. The synthesis and cyclisation of 2-bromo-3-ethoxypropanones. University College Dublin, 1998.

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12

de, Meijere A., ed. Small ring compounds in organic synthesis III. Springer-Verlag, 1988.

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13

Zugrăvescu, Ion. Cicloadiții 3+2 dipolare. Editura Academiei Republicii Socialiste România, 1987.

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14

Hunt, Ian R. Ring formation reactions: Aspects of the aqueous Diels-Alder reaction. University ofEast Anglia, 1990.

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15

Zadrożna, Irmina. Modyfikacja struktury wybranych układów cyklicznych i policyklicznych w celu uzyskania odpowiednich właściwości optycznych, fotochemicznych i biologicznych. Oficyna Wydawnicza PW, 2001.

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16

Friedrich, Schmidt. Untersuchungen zur Stereo- und Regioselektivität bei der Photodimerisierung trans-fixierter Stilbene. Schäuble, 1992.

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17

Hesse, Manfred. Ring enlargement in organic chemistry. VCH, 1991.

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18

Joseph Johannes Gerardus Steven van Es. 1, 3-cycloaddition reactions of diphenylphosphinoyl-activated azomethine ylides and 2-azaallyl anions: Synthetic applications and mechanistic aspects. Pasmans Offsetdrukkerij BV, 1992.

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19

W, Chen M., and United States. National Aeronautics and Space Administration., eds. Ion radial diffusion in an electrostatic impulse model for stormtime ring current formation. Engineering and Technology Group, The Aerospace Corp., 1992.

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20

Swinger, Joe. Leave your nose ring at home: Get the job you want by creating a powerful first impression. Career Press, 2006.

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21

Boger, Dale L. Hetero Diels-Alder methodology inorganic synthesis. Academic Press, 1987.

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22

Boger, Dale L. Hetero Diels-Alder methodology in organic synthesis. Academic Press, 1987.

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23

Maier, Martin. Hetero-Diels-Alder Reaktionen mit inversem Elektronenbedarf zur Synthese von Hexopyranosiden. Hartung-Gorre, 1985.

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24

John, Struck-Marcell Curtis, and United States. National Aeronautics and Space Administration., eds. Theoretical models of gas dymnamics in star formation in interacting ring galaxies: Final technical report. National Aeronautics and Space Administration, 1990.

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25

Li, Jie Jack. Name Reactions for Carbocyclic Ring Formations. Wiley & Sons, Incorporated, John, 2010.

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26

Hesse, Manfred. Ring Enlargement in Organic Chemistry. Wiley & Sons, Incorporated, John, 1991.

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27

Tebby, John C., Irina A. Maretina, and Boris I. Ionin. Alkynes in Cycloadditions. Wiley & Sons, Limited, John, 2013.

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28

Maretina, Irina A. Alkynes in Cycloadditions. Wiley & Sons, Incorporated, John, 2013.

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29

Tebby, John C., Irina A. Maretina, and Boris I. Ionin. Alkynes in Cycloadditions. Wiley & Sons, Incorporated, John, 2013.

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30

Tebby, John C., Irina A. Maretina, and Boris I. Ionin. Alkynes in Cycloadditions. Wiley & Sons, Incorporated, John, 2013.

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31

Tebby, John C., Irina A. Maretina, and Boris I. Ionin. Alkynes in Cycloadditions. Wiley & Sons, Incorporated, John, 2013.

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32

Li, Jie Jack, and E. J. Corey. Name Reactions for Carbocyclic Ring Formations. Wiley & Sons, Incorporated, John, 2010.

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33

Harmata, M. Advances in Cycloaddition, Volume 4 (Advances in Cycloaddition). JAI Press, 1997.

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34

Cyclometalation reactios five-membered ring products as universal reagents. Springer, 2014.

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35

Omae, Iwao. Cyclometalation Reactions: Five-Membered Ring Products as Universal Reagents. Springer, 2014.

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36

Omae, Iwao. Cyclometalation Reactions: Five-Membered Ring Products as Universal Reagents. Springer, 2016.

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37

Omae, Iwao. Cyclometalation Reactions: Five-Membered Ring Products As Universal Reagents. Springer London, Limited, 2014.

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38

Keehn, Philip. Cyclophanes. Elsevier Science & Technology Books, 2012.

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39

Ruder, Suzanne Marie. Stereoselective ring expansions of cyclopropylcarbinols. 1986.

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40

Ring Nitrogen Key Biomolecules. Chapman & Hall, 2001.

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41

Harmata, M. Advances in Cycloaddition, Volume 6 (Advances in Cycloaddition). JAI Press, 1999.

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42

D’hooghe, Matthias, and Hyun-Joon Ha. Synthesis of 4- to 7-membered Heterocycles by Ring Expansion: Aza-, oxa- and thiaheterocyclic small-ring systems. Springer, 2015.

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43

Ha, Hyun-Joon, and Matthias D'hooghe. Synthesis of 4- to 7-Membered Heterocycles by Ring Expansion: Aza-, Oxa- and Thiaheterocyclic Small-Ring Systems. Springer London, Limited, 2015.

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44

D’hooghe, Matthias, and Hyun-Joon Ha. Synthesis of 4- to 7-membered Heterocycles by Ring Expansion: Aza-, oxa- and thiaheterocyclic small-ring systems. Springer, 2019.

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45

Busch, Kenneth W., and Marianna A. Busch. Chiral Analysis. Elsevier Science & Technology Books, 2011.

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46

Cycloaddition Reactions: Advances in Research and Applications. Nova Science Publishers, Incorporated, 2019.

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47

Margetic, Davor. Cycloaddition Reactions: Advances in Research and Applications. Nova Science Publishers, Incorporated, 2019.

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48

Wempe, Michael F. The transannular rearrangement of 5-cyclodecynone. 1993.

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49

Nishiwaki, Nagatoshi. Methods and Applications of Cycloaddition Reactions in Organic Syntheses. Wiley & Sons, Incorporated, John, 2014.

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50

Methods And Applications Of Cycloaddition Reactions In Organic Syntheses. John Wiley & Sons Inc, 2014.

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