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In an attempt to design new reagents for the chemical development of latent fingerprints, a number of ninhydrin analogues were synthesized and their reactions with latent fingerprints on paper were studied. The ring-fused and substituted ninhydrins developed latent fingerprints with a sensitivity similar to that of ninhydrin. The most promising of the group was 2,2-dihydroxybenz[f]indane-1,3-dione, which developed latent fingerprints as dark green images with excellent resolution.
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Stored only when both papers are in the corpus — 63 citations exist upstream.
Papers that cite the same references — the relational fallback while embeddings are still backfilling.
Imported from OpenAlex (CC0) — nothing here is generated.