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Book Categories |
| Ch. 1 | Introduction | 1 |
| Ch. 2 | Amino acids | 11 |
| Ch. 3 | Microbial pathway engineering for amino acid manufacture | 31 |
| Ch. 4 | Carbohydrates in synthesis | 47 |
| Ch. 5 | Terpenes : the expansion of the chiral pool | 59 |
| Ch. 6 | Resolutions at large scale : case studies | 75 |
| Ch. 7 | New developments in crystallization-induced resolution | 97 |
| Ch. 8 | The role of cis-1-amino-2-indanol in resolution processes | 117 |
| Ch. 9 | Asymmetric oxidations | 123 |
| Ch. 10 | Asymmetric epoxidation of olefins by chiral ketones | 147 |
| Ch. 11 | Ozonolysis in the production of chiral fine chemicals | 165 |
| Ch. 12 | Transition metal catalyzed hydrogenations, isomerizations, and other reactions | 185 |
| Ch. 13 | Modular, chiral P-heterocycles in asymmetric catalysis | 249 |
| Ch. 14 | Asymmetric olefin hydrogenation using monodentate BINOL- and bisphenol-based ligands : phosphonites, phosphites, and phosphoramidites | 269 |
| Ch. 15 | Asymmetric catalytic hydrogenation reactions with ferrocene-based diphosphine ligands | 287 |
| Ch. 16 | Asymmetric reduction of prochiral ketones catalyzed by oxazaborolidines | 305 |
| Ch. 17 | cis-1-amino-2-indanol-derived ligands in asymmetric catalysis | 319 |
| Ch. 18 | Enantioselective hydrogenation of activated ketones using heterogeneous Pt catalysts modified with cinchona alkaloids | 345 |
| Ch. 19 | Biotransformations : "green" processes for the synthesis of chiral fine chemicals | 359 |
| Ch. 20 | Combining enzyme discovery and evolution to develop biocatalysts | 405 |
| Ch. 21 | One-pot synthesis and the integration of chemical and biocatalytic conversions | 419 |
| Ch. 22 | Substitution reactions | 429 |
| Ch. 23 | Industrial applications of chiral auxiliaries | 443 |
| Ch. 24 | The role and importance of cis-1-amino-2-indanol in biological systems and asymmetric processes | 457 |
| Ch. 25 | Enantiopure amines by chirality transfer using (R)-phenylglycine amide | 487 |
| Ch. 26 | Pericyclic reactions | 503 |
| Ch. 27 | Asymmetric free-radical reductions mediated by chiral stannanes, germanes, and silanes | 531 |
| Ch. 28 | Metathesis reactions | 539 |
| Ch. 29 | Synthesis of homochiral compounds : a small company's role | 559 |
| Ch. 30 | Commercial synthesis of the antiglaucoma prostanoid travoprost | 573 |
| Ch. 31 | Synthesis of large volume products | 589 |
| Price | Condition | Delivery | Seller | Action |
| $99.99 | Digital |
| WonderClub |
Edward Wojan
reviewed Handbook of Chiral Chemicals on October 02, 2020
Handbook of Chiral Chemicals
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