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This review addresses a literature gap by exploring the synthesis and applications of aminals, with a focus on drug discovery and molecular diversity. Beyond medicinal chemistry, aminals find applications as key components in bioactive compounds and as versatile tools in materials chemistry. The review covers fundamental characteristics, synthetic methodologies, stability, and applications, emphasizing alternative synthetic methods to the well-established aldehyde\u2013amine condensation. This inclusive exploration provides insights into diverse synthetic pathways that expand the versatility of the aminal scaffold.<\/jats:p><jats:p>1 \tIntroduction<\/jats:p><jats:p>2 \tThe Aminal Group<\/jats:p><jats:p>3 \tAminal Synthesis<\/jats:p><jats:p>3.1 \tMetal-Free Approaches<\/jats:p><jats:p>3.2 \tMetal-Catalyzed Approaches<\/jats:p><jats:p>3.3 \tPhotoredox Methodologies<\/jats:p><jats:p>3.4 \tVia Rearrangements<\/jats:p><jats:p>3.5 \tVia Decarboxylative Coupling<\/jats:p><jats:p>4 \tAminals as Synthetic Tools<\/jats:p><jats:p>5 \tSynthesis of Aminal-Containing Natural Products<\/jats:p><jats:p>6 \tAminal-Based Materials<\/jats:p><jats:p>7 \tConclusions<\/jats:p>","DOI":"10.1055\/a-2317-6604","type":"journal-article","created":{"date-parts":[[2024,4,30]],"date-time":"2024-04-30T22:54:10Z","timestamp":1714517650000},"page":"2933-2954","source":"Crossref","is-referenced-by-count":6,"title":["Progress on the Synthesis and Applications of Aminals: Scaffolds for Molecular Diversity"],"prefix":"10.1055","volume":"56","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7235-0083","authenticated-orcid":false,"given":"Rafael","family":"Rippel","sequence":"first","affiliation":[]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8474-3925","authenticated-orcid":false,"given":"Lu\u00edsa M.","family":"Ferreira","sequence":"additional","affiliation":[]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7312-8596","authenticated-orcid":false,"given":"Paula S.","family":"Branco","sequence":"additional","affiliation":[]}],"member":"194","published-online":{"date-parts":[[2024,6,10]]},"reference":[{"key":"ref1","doi-asserted-by":"crossref","first-page":"1537","DOI":"10.1055\/a-1713-8481","volume":"54","author":"T J Paris","year":"2022","journal-title":"Synthesis"},{"key":"ref2","doi-asserted-by":"crossref","first-page":"5747","DOI":"10.1021\/acscatal.6b01725","volume":"6","author":"Y Y Huang","year":"2016","journal-title":"ACS Catal."},{"key":"ref3","doi-asserted-by":"crossref","first-page":"1203","DOI":"10.1055\/a-1684-0772","volume":"54","author":"X Y Ma","year":"2022","journal-title":"Synthesis"},{"key":"ref4","doi-asserted-by":"crossref","first-page":"20","DOI":"10.1002\/chem.202002637","volume":"27","author":"R L\u00f3pez","year":"2021","journal-title":"Chem. 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