Name Reactions: A Collection of Detailed Reaction MechanismsSpringer Science & Business Media, 2003/08/04 - 465 ページ The second edition includes five points of improvement: (a) Additional 16 name reactions have been supplemented; (b) I have corrected typos and a few dubious mechanisms in the first edition. I wish to thank Prof. Rick L. Danheiser of Massa chusetts Institute of Technology and Mr. Yiqian Lian of Michigan State Univer sity for invaluable comments and suggestions. I have also incurred many debts of gratitude to Prof. Brian. M. Stoltz of California Institute of Technology and his students, Eric Ashley, Doug Behenna, Dan Caspi, Neil Garg, Blake Greene, Jeremy May, Sarah Spessard, Uttam Tambar, Raissa Trend, and Ryan Zeidan for proofreading the final draft of the second edition; (c) The references are expanded and updated; (d) A more thorough index has been implemented so the reader may navigate through the book more easily; (e) The short descriptions of name reactions given as mnemonics seem to be helpful to both novices and veterans. As a result, I added the descriptions for most reactions. Finally, I am grateful for permission to use the postage stamps on the inner covers from respective postal authorities, who still retail the copyrights of those stamps. Jack Li Ann Arbor, Michigan, May 2003 Preface to the first edition What's in a name? That which we call a rose by any other name would smell as 1 sweet. |
目次
II | 1 |
III | 2 |
IV | 3 |
V | 4 |
VI | 6 |
VII | 8 |
VIII | 9 |
IX | 10 |
CLXVI | 230 |
CLXVII | 231 |
CLXVIII | 233 |
CLXIX | 235 |
CLXX | 236 |
CLXXI | 237 |
CLXXII | 238 |
CLXXIII | 239 |
X | 11 |
XI | 13 |
XII | 14 |
XIII | 16 |
XIV | 17 |
XV | 18 |
XVI | 19 |
XVII | 20 |
XVIII | 21 |
XIX | 22 |
XX | 23 |
XXI | 24 |
XXII | 26 |
XXIII | 28 |
XXIV | 29 |
XXV | 31 |
XXVI | 32 |
XXVII | 33 |
XXVIII | 34 |
XXIX | 36 |
XXX | 38 |
XXXI | 39 |
XXXII | 40 |
XXXIII | 41 |
XXXIV | 42 |
XXXV | 43 |
XXXVI | 44 |
XXXVII | 45 |
XXXVIII | 46 |
XXXIX | 47 |
XL | 48 |
XLI | 49 |
XLII | 51 |
XLIII | 52 |
XLIV | 53 |
XLV | 54 |
XLVI | 56 |
XLVII | 57 |
XLVIII | 58 |
XLIX | 59 |
L | 60 |
LI | 61 |
LII | 62 |
LIII | 63 |
LIV | 65 |
LV | 66 |
LVI | 67 |
LVII | 68 |
LVIII | 69 |
LIX | 71 |
LX | 72 |
LXI | 73 |
LXII | 74 |
LXIII | 76 |
LXIV | 77 |
LXV | 79 |
LXVI | 82 |
LXVII | 83 |
LXVIII | 84 |
LXIX | 86 |
LXX | 88 |
LXXI | 90 |
LXXII | 92 |
LXXIII | 93 |
LXXIV | 95 |
LXXV | 96 |
LXXVI | 97 |
LXXVII | 98 |
LXXVIII | 99 |
LXXIX | 100 |
LXXX | 102 |
LXXXI | 103 |
LXXXII | 104 |
LXXXIII | 105 |
LXXXIV | 107 |
LXXXV | 109 |
LXXXVI | 110 |
LXXXVII | 111 |
LXXXVIII | 113 |
LXXXIX | 114 |
XC | 115 |
XCI | 117 |
XCII | 119 |
XCIII | 120 |
XCIV | 123 |
XCV | 125 |
XCVI | 126 |
XCVII | 127 |
XCVIII | 128 |
XCIX | 129 |
C | 130 |
CI | 132 |
CII | 134 |
CIII | 135 |
CIV | 136 |
CV | 137 |
CVI | 138 |
CVII | 139 |
CVIII | 140 |
CIX | 142 |
CX | 144 |
CXI | 145 |
CXII | 147 |
CXIII | 149 |
CXIV | 151 |
CXV | 152 |
CXVI | 153 |
CXVII | 155 |
CXVIII | 156 |
CXIX | 157 |
CXX | 158 |
CXXI | 160 |
CXXII | 161 |
CXXIII | 162 |
CXXIV | 163 |
CXXV | 164 |
CXXVI | 166 |
CXXVII | 168 |
CXXVIII | 169 |
CXXIX | 171 |
CXXX | 172 |
CXXXI | 174 |
CXXXII | 175 |
CXXXIII | 177 |
CXXXIV | 181 |
CXXXV | 182 |
CXXXVI | 183 |
CXXXVII | 186 |
CXXXVIII | 187 |
CXXXIX | 189 |
CXL | 191 |
CXLI | 192 |
CXLII | 193 |
CXLIII | 194 |
CXLIV | 196 |
CXLV | 198 |
CXLVI | 200 |
CXLVII | 202 |
CXLVIII | 203 |
CXLIX | 204 |
CL | 206 |
CLI | 208 |
CLII | 209 |
CLIII | 211 |
CLIV | 213 |
CLV | 215 |
CLVI | 217 |
CLVII | 218 |
CLVIII | 219 |
CLIX | 220 |
CLX | 222 |
CLXI | 223 |
CLXII | 225 |
CLXIII | 226 |
CLXIV | 227 |
CLXV | 228 |
CLXXIV | 240 |
CLXXV | 241 |
CLXXVI | 242 |
CLXXVII | 243 |
CLXXVIII | 244 |
CLXXIX | 245 |
CLXXX | 246 |
CLXXXI | 248 |
CLXXXII | 249 |
CLXXXIII | 251 |
CLXXXIV | 253 |
CLXXXV | 254 |
CLXXXVI | 255 |
CLXXXVII | 256 |
CLXXXVIII | 258 |
CLXXXIX | 259 |
CXC | 260 |
CXCI | 261 |
CXCII | 262 |
CXCIII | 263 |
CXCIV | 264 |
CXCV | 265 |
CXCVI | 266 |
CXCVII | 267 |
CXCVIII | 269 |
CXCIX | 270 |
CC | 272 |
CCI | 274 |
CCII | 275 |
CCIII | 277 |
CCIV | 279 |
CCV | 280 |
CCVI | 281 |
CCVII | 282 |
CCVIII | 283 |
CCIX | 284 |
CCX | 286 |
CCXI | 287 |
CCXII | 289 |
CCXIII | 290 |
CCXIV | 291 |
CCXV | 293 |
CCXVI | 294 |
CCXVII | 295 |
CCXVIII | 296 |
CCXIX | 298 |
CCXX | 299 |
CCXXI | 300 |
CCXXII | 302 |
CCXXIII | 303 |
CCXXIV | 304 |
CCXXV | 305 |
CCXXVI | 307 |
CCXXVII | 310 |
CCXXVIII | 311 |
CCXXIX | 312 |
CCXXX | 314 |
CCXXXI | 315 |
CCXXXII | 316 |
CCXXXIII | 317 |
CCXXXIV | 319 |
CCXXXV | 320 |
CCXXXVI | 322 |
CCXXXVII | 323 |
CCXXXVIII | 324 |
CCXXXIX | 325 |
CCXL | 327 |
CCXLI | 328 |
CCXLII | 329 |
CCXLIII | 330 |
CCXLIV | 332 |
CCXLV | 334 |
CCXLVI | 336 |
CCXLVII | 337 |
CCXLVIII | 339 |
CCXLIX | 340 |
CCL | 341 |
CCLI | 343 |
CCLII | 344 |
CCLIII | 345 |
CCLIV | 346 |
CCLV | 347 |
CCLVI | 349 |
CCLVII | 351 |
CCLVIII | 352 |
CCLIX | 354 |
CCLX | 355 |
CCLXI | 356 |
CCLXII | 357 |
CCLXIII | 359 |
CCLXIV | 361 |
CCLXV | 362 |
CCLXVI | 363 |
CCLXVII | 364 |
CCLXVIII | 366 |
CCLXIX | 369 |
CCLXX | 372 |
374 | |
CCLXXII | 375 |
CCLXXIII | 376 |
CCLXXIV | 378 |
CCLXXV | 380 |
CCLXXVI | 381 |
383 | |
CCLXXVIII | 384 |
CCLXXIX | 386 |
CCLXXX | 387 |
CCLXXXI | 389 |
CCLXXXII | 391 |
CCLXXXIII | 392 |
CCLXXXIV | 393 |
CCLXXXV | 394 |
CCLXXXVI | 396 |
CCLXXXVII | 397 |
398 | |
CCLXXXIX | 399 |
CCXC | 401 |
CCXCI | 402 |
CCXCII | 404 |
CCXCIII | 405 |
407 | |
CCXCV | 408 |
CCXCVI | 409 |
CCXCVII | 411 |
CCXCVIII | 412 |
414 | |
CCC | 415 |
CCCI | 416 |
418 | |
CCCIII | 419 |
CCCIV | 421 |
CCCV | 422 |
424 | |
CCCVII | 426 |
CCCVIII | 427 |
CCCIX | 428 |
CCCX | 429 |
CCCXI | 431 |
432 | |
CCCXIII | 433 |
437 | |
438 | |
439 | |
440 | |
441 | |
443 | |
444 | |
CCCXXI | 445 |
447 | |
CCCXXIII | 448 |
450 | |
CCCXXV | 451 |
CCCXXVI | 453 |
455 | |
他の版 - すべて表示
多く使われている語句
acid Acta acyl addition AICI3 alcohols aldehydes aldol alkyl amines Angew Asymmetric Asymmetric Synthesis Bull carbonyl catalytic cycle CCl3 CH3O Chem Chim CO₂ CO₂CH3 CO₂Et CO₂Et CO₂Et CO₂H CO₂Me Commun condensation cross-coupling reaction cyclization cycloaddition deprotonation Dtsch elimination Engl enolate ester EtO2C formation Grignard reagents H H+ H OH H References H+ H H₂N H₂O Heterocycl hydrolysis indole synthesis intermediate Justus Liebigs Justus Liebigs Ann ketones M. J. Chem N₂ NH₂ nucleophilic O₂N OH OH olefins OR¹ Organic Synthesis Organomet oxidation Perkin Trans Ph Ph Pharm Pivo PPh3 Prakt Prep R¹ H R¹ R¹ R¹ R2 R¹ References R¹O R2 H R2 R¹ React reagent rearrangement reductive Review Synlett Synth Synthesis 2002 tautomerization Tetrahedron 1998 Tetrahedron 2000 Tetrahedron Lett transmetallation Wang workup Zhang