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1

Jack, Li Jie, ed. Name reactions for carbocyclic ring formations. Hoboken, N.J: Wiley, 2010.

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2

1933-, Tebby John C., ed. Alkynes in cycloadditions. Chichester, West Sussex: Wiley, 2014.

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3

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

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4

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

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5

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

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6

Valters, Raimonds E. Ring-chain tautomerism. New York: Plenum, 1985.

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7

Wilhelm, Flitsch, and Katritzky Alan R, eds. Ring-chain tautomerism. New York: Plenum Press, 1985.

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8

Margetic, Davor. Microwave assisted cycloaddition reactions. Hauppauge, N.Y: Nova Science Publishers, 2012.

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9

Harmata, Michael. Advances in cycloaddition. Stamford, Conn: JAI Press, 1999.

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10

Horst, Kunz, ed. Chiral auxiliaries in cycloadditions. Weinheim: Wiley-VCH, 1999.

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11

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

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12

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

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13

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

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14

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

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15

Y, Thebtaranonth, ed. Cyclization reactions. Boca Raton: CRC Press, 1994.

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16

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

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17

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

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18

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

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19

Ring nitrogen and key biomolecules: The biochemistry of N-heterocycles. Dordrecht: Kluwer Academic, 1998.

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20

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

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21

Carbocycle construction in terpene synthesis. New York, N.Y: VCH, 1988.

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22

Overlap determinant method in the theory of pericyclic reactions. Berlin: Springer, 1995.

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23

1922-, Singer B., Bartsch H, International Agency for Research on Cancer., National Cancer Institute (U.S.), and Lawrence Berkeley Laboratory, eds. The Role of cyclic nucleic acid adducts in carcinogenesis and mutagenesis: Proceedings of a meeting organized by the IARC and co-sponsored by the US National Cancer Institute, and the Lawrence Berkeley Laboratory at the University of California, held in Lyon, 17-19 September 1984. Lyon: International Agency for Research on Cancer, 1986.

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24

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

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25

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

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26

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

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27

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

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28

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

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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

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

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31

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

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32

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

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33

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

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34

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

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35

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

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36

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

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37

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

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38

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

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39

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

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40

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

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41

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

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42

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

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43

Ring Nitrogen Key Biomolecules. Chapman & Hall, 2001.

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44

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

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45

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

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46

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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47

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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48

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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49

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

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50

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

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