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. 2009 Dec 5;7(1):19–28. doi: 10.7150/ijms.7.19

Figure 1.

Figure 1

Simplified mechanistic illustration of the electron rearrangement during DARinv. While the first step of association between diene and dienophile is reversible, the release of nitrogen during rearrangement of the intermediate product is irreversible and switches the reaction to the product side.