Heterocyclic chemistry
著者
書誌事項
Heterocyclic chemistry
Chapman & Hall, 1995
3rd ed
並立書誌 全1件
大学図書館所蔵 全4件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
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  イギリス
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注記
Previous ed.: 1978
Includes bibliographies and index
内容説明・目次
内容説明
3. 4 Electrocyclic processes in heterocyclic ring synthesis 61 3. 5 Nitrenes in heterocyclic ring synthesis 62 References for chapter 3 63 4 Typical reactivity of pyridines, quinolines and isoquinolines 64 5 Pyridines: reactions and synthesis 72 5. 1 Reactions with electrophilic reagents 73 5. 2 Reactions with oxidising agents 79 5. 3 Reactions with nucleophilic reagents 80 5. 4 Reactions with bases 82 5. 5 Reactions of C-metallated pyridines 83 5. 6 Reactions with radical reagents 85 5. 7 Reactions with reducing agents 86 5. 8 Electrocyclic reactions (ground state) 87 5. 9 Photochemical reactions 88 5. 10 Oxy-and aminopyridines 89 5. 11 Alkylpyridines 94 5. 12 Pyridine aldehydes, ketones, carboxylic acids and esters 95 5. 13 Quatemary pyridinium salts 95 5. 14 Pyridine N -oxides 10 1 5. 15 Synthesis of pyridines 104 References for chapter 5 111 Exercises for chapter 5 118 6 Quinolines and isoquinolines: reactions and synthesis 120 6. 1 Reactions with electrophilic reagents 121 6. 2 Reactions with oxidising agents 123 6. 3 Reactions with nucleophilic reagents 123 6. 4 Reactions with bases 125 6. 5 Reactions of C-metallated quinolines and isoquinolines 126 6.
6 Reactions with radical reagents 126 6. 7 Reactions with reducing agents 126 6. 8 Electrocyclic reactions (ground state) 127 6. 9 Photochemical reactions 128 6. 10 Oxyquinolines and -isoquinolines 128 6. 11 Aminoquinolines and -isoquinolines 130 6. 12 Alkylquinolines and -isoquinolines 130 6.
目次
- Part 1 Structures and main physical properties of aromatic heterocycles: reactivity of aromatic heterocycles
- synthesis of aromatic heterocycles
- typical reactivity of pyridines, quinolines and isoquinolines
- pyridines - reactions and synthesis
- quinolines and isoquinolines - reactions and synthesis. Part 2 Typical reactivity of pyryliums and benzopyryliums: pyryliums, 2- and 4-pyrones - reactions and synthesis
- benzopyryliums, benzo-pyrones - reactions and synthesis
- typical reactivity of diazines - pyridazine, pyrimidine and pyrazine, and their benzo-analogues
- the diazines - pyridazine, pyrimidine and pyrazine - reactions and synthesis
- typical reactivity of pyrroles, thiophens and furans
- pyrroles - reactions and synthesis
- thiophenes - reactions and synthesis
- furans - reactions and synthesis
- typical reactivity of indoles, isoindoles and bvenzothiophens and benzofurans
- indoles - reactions and synthesis
- benzo[b]thiophens and benzo[b]furans - reactions and synthesis
- isoindoles, benzo[c]thiophens and isobenzofurans - reactions and synthesis
- typical reactivity of 1,3- and 1,2-azoles
- 1,3-azoles - imidazoles, thiazoles and oxazoles - reactions and synthesis
- 1,2-azoles - pyrazoles, isothiazoles, isoxazoles - reactions and synthesis
- purines - reactions and synthesis
- heterocycles containing a ring-junction nitrogen
- heterocycles with more than two heteroatoms
- saturated and partially unsaturated heterocyclic compounds - reactions and synthesis.
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