Organic Syntheses

Online ISBN: 9780471264224

DOI: 10.1002/0471264229

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  27. 0-9
  1. (S)-1-(Furan-2-yl)ethanol
  2. (S)-2-Amino-4-methyl-1,1-diphenylpentan-1-ol
  3. (S)-5-Oxo-5,6-dihydro-2H-pyran-2-yl benzoate
  4. (S)-8a-Methyl-3,4,8,8a-tetrahydro-1,6(2H,7H)-napht
  5. (S)-COP-OAc dimer
  6. (S)-N-[(S-1-Hydroxy-4-methyl-1,1-diphenylpentan-2-
  7. (S)-Proline
  8. (S)-tert-Butyl (1-(benzylamino)-4-methyl-1-oxopent
  9. (S,S)-Diisopropyl tartrate (E)-crotylboronate
  10. (Sa,S)-N-[2'-(4-Methylphenylsulfonamido)-1,1'-bina
  11. Safety
  12. Salicyaldehydes
  13. Sandmeyer approach
  14. Saponification
  15. Scalable method
  16. Scalable protocols
  17. Schlenk techniques
  18. Schwartz's reagent
  19. SE
  20. Secondary amines
  21. Secondary electrophiles
  22. Secondary phosphine oxides
  23. Secondary phosphines
  24. SEGPHOS
  25. Selective fluorination
  26. Selenation
  27. Semiconducting organic material
  28. Separation
  29. Side chain
  30. Sigmatropic
  31. Silicon-based reagents
  32. Siloles
  33. Siloxy alkynes
  34. Silver
  35. Silver nitrate
  36. Silver tetraborate
  37. Silver-catalyzed rearrangement
  38. Silyl enol ethers
  39. Silylation
  40. Silylglyoxylates
  41. Single step synthesis
  42. Single-step preparation
  43. Skattebol's synthesis
  44. Smiles rearrangement
  45. SN
  46. SN 1
  47. SN 2
  48. SN'
  49. SNAr
  50. Sodium azide
  51. Sodium cyanoborohydride
  52. Sodium formate
  53. Solid-liquid phase
  54. Solubility
  55. Solvolysis
  56. SOMO Catalysis
  57. Sonication
  58. Sonogashira coupling
  59. Sonogashira coupling-addition-cyclocondensation
  60. Sonogshira coupling
  61. Spiroborate eters
  62. Spirocycle formation
  63. Spirocyclohexyloxazolidinone
  64. Stabilization
  65. Stang's reagent
  66. Stannylation
  67. Staudinger reaction
  68. Stereochemical configuration
  69. Stereoconvergent cross coupling
  70. Stereoconvergent Negishi cross coupling
  71. Stereoselctive synthesis
  72. Stereoselective
  73. Stereoselective annulations
  74. Stereoselective synthesis
  75. Steroids
  76. Stoichiometric oxidations
  77. Storage
  78. Styryl iodide
  79. Subambient temperatures
  80. Substituted arynes
  81. Substituted azaindoles
  82. Substituted benzoxazoles
  83. Substituted cyclopropanols
  84. Substituted pyrazoles
  85. Substitution
  86. Substrate scope
  87. Substrates
  88. Sugars. Per-O-acetylation
  89. Sulfenylation
  90. Sulfonamides
  91. Sulfones
  92. Sulfonyl azides
  93. Sulfonylamides
  94. Sulfoxides
  95. Sulfuric acid
  96. Sulphonation
  97. Sulphurisation
  98. Suzuki coupling
  99. Suzuki reaction
  100. Suzuki-Miyaura coupling
  101. Suzuki-miyaura cross-coupling
  102. Suzuki-miyura reaction
  103. Synthetic intermediates
  104. Synthons
  105. syn-Additions
  106. S-Acylation
  107. S-Alkylation
  108. S-Amination
  109. S-Arylation
  110. S-Benzyl isothiouronium chloride
  111. S-Deacylation
  112. S-Dealkylation
  113. S-Debenzylation
  114. S-Deoxygenation
  115. S-Deprotection
  116. S-Desulphurisation
  117. S-Methylation
  118. S-Oxidation
  119. S-Protection
  120. S-Sulphurisation
  121. s-Triazine

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