Organic Syntheses

Online ISBN: 9780471264224

DOI: 10.1002/0471264229

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  27. 0-9
  1. C7-Boronated 3-substituted indole derivatives
  2. C7-Functionalization
  3. Cadiot-chodkiewicz coupling
  4. Cannulation
  5. Carbamates
  6. Carbamidomethylation
  7. Carbazole-based macrocycle
  8. Carbene
  9. Carbene precursors
  10. Carbodicarbene
  11. Carbodiimides
  12. Carbon monoxide
  13. Carbon nucleophiles
  14. Carbonium
  15. Carbonyl alpha-oxidation
  16. Carbonyl benzyloxycyanamide
  17. Carbonyl carbon-silicon bond
  18. Carbonyl compounds
  19. Carbonylation
  20. Carbon-accelerated claisen rearrangement
  21. Carbon-carbon bond forming reactions
  22. Carbon-carbon bonds
  23. Carboxylates
  24. Carboxylation
  25. Carboxylic acid
  26. Cascade catalysis
  27. Catalysis
  28. Catalyst
  29. Catalysts
  30. Catalytic addition
  31. Catalytic asymmetric addition
  32. Catalytic asymmetric arylation
  33. Catalytic cycle
  34. Catalytic eantioselective
  35. Catalytic reduction
  36. Catalyzed amidation
  37. Catalyzed decarboxylativeammination
  38. Catalyzed diamination
  39. Cesium acetate
  40. Cesium carbonate
  41. Chemioslective deprotection
  42. Chemoselective
  43. Chemo-selectivity
  44. Chiral 2-oxazolines
  45. Chiral alcohols
  46. Chiral allenamides
  47. Chiral allenes
  48. Chiral allylmetal reagent
  49. Chiral amines
  50. Chiral amino carbonyl compounds
  51. Chiral auxiliary
  52. Chiral bromodialkylsulfonium bromide
  53. Chiral bronsted acids
  54. Chiral complex
  55. Chiral complexes
  56. Chiral crotylmetal reagent
  57. Chiral diamines
  58. Chiral intermediates
  59. Chiral ligands
  60. Chiral lithium amide bases
  61. Chiral organoboranes
  62. Chiral pyridyl amines
  63. Chiral tetramic acids
  64. Chiral triazolium salts
  65. Chiral ynamide
  66. Chloral synthon
  67. Chlorhydrin
  68. Chlorination
  69. Chlorine atom
  70. Chloroacrolein Diethyl acetal
  71. Chlorodimethylsulfonium chloride
  72. Chloroform
  73. Chloroiodopyridines
  74. Chloroketones
  75. Chloroquine
  76. Chlorosilanes
  77. Chlorotitanium enolate
  78. Cholesta-3,5-diene
  79. Chromatographic purification
  80. Chromophores
  81. Cinchona alkaloids
  82. Cinchonidinium bromide
  83. Cinnamyl H-phosphinic acid
  84. cis-5-Aryl-3-alkenoates
  85. Cleavage
  86. Cobalt catalyst
  87. Cobalt complexes
  88. Complexation
  89. Condensation
  90. Condensative synthesis
  91. Conjugate addition
  92. Conjugate additions
  93. Conjugate trienes
  94. Conjugated dienes
  95. Conjugation
  96. Conjunctive reagent
  97. Contaminants
  98. COP catalysts
  99. Cope rearrangement
  100. Copper (I) iodide
  101. Copper (II) complex
  102. Copper (II) triflate
  103. Copper bromide dimethylsulfide
  104. Copper catalyst
  105. Copper catalyzed alkynylation
  106. Copper catalyzed electrophilic amination
  107. Copper iodide
  108. Copper/palladium catalyst
  109. Copper-catalysis
  110. Copper-catalyzed conjugate addition reactions
  111. Copper-mediated aryl amination
  112. Copper-mediated coupling
  113. Copper-mediated oxidative coupling
  114. Copper-mediated synthesis
  115. Copper-promoted reactions
  116. Coumalic acid
  117. Coupling
  118. Cp2ZrHCl
  119. Cross coupling
  120. Cross coupling reaction
  121. Cross-coupling
  122. Cross-coupling strategy
  123. Cross-couplings
  124. Crystalline (Diisopinocampheyl) borane
  125. CuCl2 mediated aza-oxindole synthesis
  126. Curphey procedure
  127. Curtius rearrangement
  128. Cu-Catalyzed azide-alkyne cycloaddition
  129. Cyanation
  130. Cyanine dyes
  131. Cyclic 1,3-diketones
  132. Cyclic alkenes
  133. Cyclic amines
  134. Cyclic enecarbamates
  135. Cyclisation
  136. Cyclization
  137. Cyclizations
  138. Cycloaddition
  139. Cycloaddition reaction
  140. Cycloadditions
  141. Cycloadducts
  142. Cyclobutarenes
  143. Cyclobutenone
  144. Cyclocondensation
  145. Cycloheptane-1,3-dione
  146. Cyclohept-4-enones
  147. Cyclohexadienes
  148. Cyclohexene imine
  149. Cycloisomerization
  150. Cyclopentanone
  151. Cyclopropanation
  152. Cyclopropane
  153. Cyclopropanone equivalent
  154. C-4 Bromination
  155. C-Acylation
  156. C-Alkylation
  157. C-Amination
  158. C-Arylation
  159. C-Benzylation
  160. C-Boration
  161. C-C Bond
  162. C-C Bond formation
  163. C-Cyanation
  164. C-Deacylation
  165. C-Dealkylation
  166. C-Deoxygenation
  167. C-Deprotection
  168. C-Desilylation
  169. C-Formylation
  170. C-H Activation
  171. C-H bonds
  172. C-H coupling reaction
  173. C-H Functionalization
  174. C-Methylation
  175. C-Nitration
  176. C-Nitrosation
  177. C-Phosphorisation
  178. C-Protection
  179. C-Silylation

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