| 000 | 04873cam a2200865Ia 4500 | ||
|---|---|---|---|
| 001 | ocn802291228 | ||
| 003 | OCoLC | ||
| 005 | 20171224114027.0 | ||
| 006 | m o d | ||
| 007 | cr cnu---unuuu | ||
| 008 | 120730s2012 gw a ob 001 0 eng d | ||
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| 020 | _z9783527330430 | ||
| 020 | _z3527330437 | ||
| 024 | 8 | _a9786613854735 | |
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_aSCI _x013040 _2bisacsh |
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| 082 | 0 | 4 |
_a547/.044 _223 |
| 049 | _aMAIN | ||
| 245 | 0 | 0 |
_aIsocyanide Chemistry : _bApplications in Synthesis and Materials Science / _cedited by Valentine Nenajdenko. |
| 260 |
_aWeinheim : _bWiley-VCH, _c2012. |
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| 300 |
_a1 online resource (xviii, 605 pages) : _billustrations |
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| 336 |
_atext _btxt _2rdacontent |
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| 337 |
_acomputer _bc _2rdamedia |
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| 338 |
_aonline resource _bcr _2rdacarrier |
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| 347 |
_adata file _2rda |
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| 380 | _aBibliography | ||
| 504 | _aIncludes bibliographical references and index. | ||
| 588 | 0 | _aPrint version record. | |
| 505 | 8 |
_6880-01 _a1.5.1 Isolation and Natural Sources1.5.2 Synthesis of Naturally Occurring Isocyanides; 1.6 Isocyanides Used in the Synthesis of Chiral Polyisocyanides; 1.6.1 Properties; 1.6.2 Synthesis; 1.6.3 Applications; References; 2: General Aspects of Isocyanide Reactivity; 2.1 Introduction; 2.2 Isocyanide-Cyanide Rearrangement; 2.3 Oxidation/Reduction of the Isocyano Group; 2.3.1 Oxidation of the Isocyano Group; 2.3.2 Reactions with Sulfur and Selenium; 2.3.3 Reduction of the Isocyano Group; 2.4 Reactions of Isocyanides with Electrophiles; 2.4.1 Reaction with Acids. |
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| 520 | _aThe efficacy of isocyanide reactions in the synthesis of natural or naturallike products has resulted in a renaissance of isocyanide chemistry. Now isocyanides are widely used in different branches of organic, inorganic, coordination, combinatorial and medicinal chemistry. This invaluable reference is the only book to cover the topic in such depth, presenting all aspects of synthetic isonitrile chemistry. The highlyexperienced and internationally renowned editor has brought together an equally distinguished team of authors who cover multicomponentreactions, isonitriles in total. | ||
| 650 | 0 |
_aIsocyanides _xSynthesis. |
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| 650 | 0 | _aChemistry, Organic. | |
| 650 | 4 | _aBioorganic chemistry. | |
| 650 | 4 | _aComplex compounds. | |
| 650 | 4 | _aIsocyanides. | |
| 650 | 4 | _aOrganometallic compounds. | |
| 650 | 7 |
_aSCIENCE _xChemistry _xOrganic. _2bisacsh |
|
| 650 | 7 |
_aIsocyanide. _0(DE-588)4162494-4 _2gnd |
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| 655 | 4 | _aElectronic books. | |
| 700 | 1 | _aNenajdenko, Valentine. | |
| 776 | 0 | 8 |
_iPrint version: _tIsocyanide chemistry. _dWeinheim : Wiley-VCH, 2012 _z9783527330430 _w(OCoLC)794035539 |
| 856 | 4 | 0 |
_uhttp://onlinelibrary.wiley.com/book/10.1002/9783527652532 _zWiley Online Library |
| 880 | 0 |
_6505-01/(S _aIsocyanide Chemistry: Applications in Synthesis and Material Science; Contents; Preface; List of Contributors; 1: Chiral Nonracemic Isocyanides; 1.1 Introduction; 1.2: Simple Unfunctionalized Isocyanides; 1.3 Isocyanides Containing Carboxylic, Sulfonyl, or Phosphonyl Groups; 1.3.1 α-Isocyano Esters; 1.3.2 α-Isocyano Amides; 1.3.3 Other Isocyano Esters or Amides; 1.3.4 Chiral Sulfonylmethyl or Phosphonylmethyl Isocyanides; 1.4 Isocyanides Containing Amino or Alcoholic Functionalities; 1.4.1 Chiral Amino or Azido Isocyanides; 1.4.2 Chiral Hydroxy Isocyanides; 1.5 Natural Isocyanides. |
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