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Atom efficiency and catalysis in organic synthesis

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Sheldon, Roger A.·2000·Pure and Applied Chemistry

Abstract

The key to waste minimization in fine chemicals manufacture is the widespread substitution of classical organic syntheses employing stoichiometric amounts of inorganic reagents with cleaner, catalytic alternatives. The E factors (by waste per kg product) of chemical processes increase dramatically on going downstream from bulk to fine chemicals and pharmaceuticals, mainly owing to the use of "stoichiometric" methods. The concept of atom efficiency is a useful tool for rapid evaluation of the amount of waste generated by alternative processes. The general theme of atom-efficient, catalytic processes is illustrated with industrially relevant examples. These include catalysis by solid acids and bases, catalytic reductions and oxidations, catalytic C_C bond formation, asymmetric catalysis, biocatalysis, and catalysis in novel media (aqueous and fluorous biphasic systems, supercritical fluids, and ionic liquids).

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Metadata

Authors
Sheldon, R. A.
Venue
Pure and Applied Chemistry
Published
2000-01-01
Volume
72
Issue
7
Pages
1233-1246
ISSN
  • 0033-4545 (ISSN-L)
  • 1365-3075
OpenAlex
W2142948768
Cited by
769
References
0
FWCI
9.33
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Atom efficiency and catalysis in organic synthesis. https://app.cochat.ai/papers/10.1351/pac200072071233
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Sheldon, R. A. (2000). Atom efficiency and catalysis in organic synthesis. Pure and Applied Chemistry. https://doi.org/10.1351/pac200072071233

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.