Topochemical reactions are solid-state reactions that transpire under the strict control of molecular packing in the crystal lattice. Due to this lattice control, these reactions generate products in a regio-/stereospecific manner and in very high yields. In a broader sense, topochemical reactions mimic nature's way of carrying out reactions in a confined environment of enzymes giving specific products. Apart from their remarkable specificity, topochemical reactions have many other interesting features that make these reactions more attractive than solution-phase reactions. Solution-phase reactions necessitate the use of reactants, reagents, catalysts, and solvents and often give products along with varying amounts of byproducts, necessitating complex workup and chromatographic purification using various chemicals. These inevitable chemical wastes from solution-state reactions could be avoided by topochemical reactions, as they are solvent-free and catalyst-free and often do not require any chromatographic purification in view of their specificity and high yielding nature. Also the confinement offered by the crystal lattice gives products that are not possible by solution-phase reactions. Another interesting feature of topochemical reactions is the possibility of formation of products in an ordered (crystalline) form, which imparts interesting properties. Thus, topochemical reactions have control not only at the molecular level (regio-/stereospecificity) but also at the supramolecular level (packing). Many topochemical reactions happen in single-crystal-to-single-crystal (SCSC) fashion, and crystal structure analysis of such reactions often gives mechanistic insights and knowledge about the geometrical criteria required for the reaction. Despite all these attractive features, reactions that can be done topochemically are limited. There is tremendous interest in the development of new categories of topochemical reactions and strategies to achieve reactivity in crystals. In this Account, we will summarize our attempts to develop topochemical azide-alkyne cycloaddition (TAAC) reactions. We have used hydrogen-bonding as the main noncovalent interaction for aligning azide-and-alkyne-substituted derivatives of various biomolecules in orientations suitable for their proximity-driven cycloaddition reaction in crystals. Overall, three major classes of biomolecules; carbohydrates, nucleosides, and peptides were successfully exploited for their TAAC reactions using conventional O-H···O, N-H···O, and N-H···N hydrogen bonds as supramolecular glues for controlling their assembly in crystals. The crystals of these monomers underwent TAAC reaction either spontaneously at room temperature or under heating yielding triazole-linked biopolymer mimics. The ordered packing of product molecules imparted special properties to the products formed. The legendary "cream of the crop" azide-alkyne click reaction has diverse applications in the areas of bioconjugation, material science, polymer synthesis, and so forth. Belonging to the same genre, TAAC is a novel metal-free approach for making the triazole-linked products employing the ordered crystal/gel as a reaction medium. In brief, our studies suggest that TAAC reaction can be implemented in diverse molecular categories and has high potential to develop into a field with practical applications.