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1

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

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2

Aldo, Taticchi, ed. Dienes in the Diels-Alder reaction. Wiley, 1990.

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3

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

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4

Knol, Jochem. Chiral Lewis acid catalyzed Diels-Alder reactions. [s.n.], 1996.

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5

Lin, Denny. Intramolecular Diels-Alder reactions of alkenylboranes & a hetero Diels-Alder approach to the total synthesis of Martinelline. National Library of Canada = Bibliothèque nationale du Canada, 1999.

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6

Ernst, Wagner. Untersuchungen zur asymmetrischen Induktion in der Hetero-Diels-Alder-Reaktion. Hartung-Gorre, 1989.

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7

Thadani, Avinash N. Alkenyl- and dienylboronate tethered intramolecular diels-alder reactions. National Library of Canada, 1998.

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8

Robertson, Andrew 1971. Recognition-mediated control of the Diels-Alder reaction. University of Birmingham, 1997.

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9

Iqbal, Sayeedha. Towards aza-macropolycycles via repetitive Diels-Alder reactions. University ofBirmingham, 1993.

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10

Linders, Joannes Theodorus Maria. Synthesis and Diels-Alder reactions of novel morphinandienes. [s.n.], 1989.

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11

Adam, I. M. Investigation of a model system for diels-alder polymerization. UMIST, 1995.

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12

Bennes, Raphaël Michel. Recognition-induced control and acceleration of Diels-Alder cycloadditions. University of Birmingham, 2000.

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13

Peglow, Thomas. Elektronentransferkatalysierte Diels-Alder-Reaktionen von Indolen mit exocyclischen Dienen. [s.n.], 1998.

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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

Moralee, Andrew Charles. The synthesis of geminally difluorinated cyclohexenols via Diels-Alder chemistry. University of Birmingham, 2001.

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16

Pies, Michael. Regio-, Diastereo- und Enantioselektivität in einer Photo-Diels-Alder-Addition. [s.n.], 1989.

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17

Oehlerking, Hans-Heinrich. Stereoselektive Darstellung von tricyclischen Oxadienonen durch intramolekulare Enin-Diels-Alder-Reaktionen. [s.n.], 1994.

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18

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

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19

Schaberg, Ralf Dieter. Darstellung methoxysubstituierter o-Benzochinone und deren Umsetzungen in Diels-Alder-Reaktionen. [s.n.], 1991.

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20

Edwards, Louise G. Studies in the nickel catalyzed [2+2+2] Homo Diels-Alder reaction. National Library of Canada, 1990.

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21

Jäger, Helge. 2-Ethinyl-1,3-Butadien: Ein neues Dien für die Diels-Alder-Reaktion. [s.n.], 1986.

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22

Gutenberg-Universität, Johannes, ed. O-Chinolacetate im Übergangsbereich zwischen Diels-Alder-Reaktionen mit normalem und inversem Elektronenbedarf. [s.n.], 1988.

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23

Goodby, Andrew James. An investigation of Diels-Alder addition across a metal bound n5-C5Me5 group. University of Salford, 1995.

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24

Kindermann, Richard. Zum Übergangszustand der Diels-Alder-Reaktionen [alpha],[beta]-ungesättigter [alpha-beta-ungesättigter] Carbonylverbindungen. [s.n.], 1989.

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25

Schulz, Frauke. Die Auswirkung arylmanipulierter Elektronendichten auf die Diels-Alder-Chemie von 4p-Systemen [4pi-Systemen]. [s.n.], 1995.

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26

Lee, Sharon Kim. Enantioselective (Formal) Aza-Diels-Alder Reactions with Danishefsky's Diene and Non-Danishefsky Type Dienes. [publisher not identified], 2012.

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27

Stansfield, Kevin. Diels-alder reactions of fluoroalkenes: New strategy and tactics in the synthesis of fluorinated carbocycles. University of Birmingham, 1996.

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28

München, Technische Universität, ed. [alpha]-[beta]-ungesättigte [Alpha-beta-ungesättigte] Carbenliganden als Synthone in der Naturstoffsynthese und der Diels-Alder-Reaktion. [s.n.], 1985.

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29

Rese, Michael. Untersuchung zum Mechanismus der Diels-Alder-Reaktion: Die Reaktion von 2,3-Bis-(N, N-dimethylaminomethylen)-bicyclo[2.2.2]oktan mit elektronenarmen Olefinen. s.n.], 1994.

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30

Santelli, Maurice. Lewis acids and selectivity in organic synthesis. CRC Press, 1996.

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31

Hisashi, Yamamoto, ed. Lewis acid reagents: A practical approach. Oxford University Press, 1999.

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32

Taber, Douglass F. Intramolecular Diels-Alder and Alder Ene Reactions. Springer, 2012.

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33

Taber, Douglass F. Intramolecular Diels-Alder and Alder Ene Reactions. Springer, 2011.

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34

Taber, Douglass F. Intramolecular Diels-Alder and Alder Ene Reactions. Springer, 2014.

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35

Parlow, John J. A foiled Diels-Alder reaction. 1987.

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36

Parlow, John J. A foiled Diels-Alder reaction. 1987.

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37

Fringuelli, Francesco, and Aldo Taticchi. Diels-Alder Reaction: Selected Practical Methods. Wiley & Sons, Incorporated, John, 2003.

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38

Fringuelli, Francesco, and Aldo Taticchi. Diels-Alder Reaction: Selected Practical Methods. Wiley & Sons, Incorporated, John, 2002.

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39

Fringuelli, Francesco, and Aldo Taticchi. Diels-Alder Reaction: Selected Practical Methods. Wiley & Sons, Incorporated, John, 2003.

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40

Hetero Diels—Alder Methodology in Organic Synthesis. Elsevier, 1987. http://dx.doi.org/10.1016/c2009-0-21747-8.

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41

Boger, Dale L., and Steven M. Weinreb. Hetero Diels-Alder Methodology in Organic Synthesis. Elsevier Science & Technology Books, 2012.

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42

Kiel, Universität, ed. Intramolekulare Diels-Alder-Reaktionen mit 1-Alkoxyisobenzofuranen. 1988.

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43

Kuhrau, Martin Gordon. Neue Polymere durch repetitive Diels-Alder Polyaddition. 1992.

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44

The Diels-Alder Reaction: Selected Practical Methods. Wiley, 2002.

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45

Hamer, Jan. 1,4-Cycloaddition Reaction : the Diels-Alder Reaction in Heterocyclic Syntheses: The Diels-Alder Reaction in Heterocyclic Syntheses. Elsevier Science & Technology Books, 2013.

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46

Kong, Sukbin. Studies on the decalin type sesquiterpenoid system: Synthetic methodologies and applications. 1985.

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47

Maitra, Uday. Part I. Selective aqueous Diels-Adler reactions ; Part II. Template directed beta-face functionalization and sidechain removal of steroids. 1986.

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48

Jackson, Mark. Diels-Alder reactions of heterocyclic fused a-pyrones. 1991.

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49

Brünjes, Rainer. Enantiomerenreine cis-Allylalkohole durch Retro-Diels-Alder-Reaktion. 1993.

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50

Sencherey, Bernard Baffour. Photochemical generation and reactions of N-acyl-1-aza-1,3-diene. 1986.

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