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1. 1b 1g

A. U. E. X. S. P. N. P. O. I. -. R. 1. 1b 1g. -. C O P E. O X I. S K R A U P. 2 . 2a 2e 2f.

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1. 1b 1g

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  1. A U E X S P N P O I - R 1. 1b 1g - C O P E O X I S K R A U P 2. 2a 2e 2f Efficientmicrowave-assistedsynthesis of quinolines and Dihydroquinolinesundersolvent-free conditions B. C. Ranu, A. Hajra, S.S. Dey, U. Jana J. Org. Chem., 2003, 59, 813-819 P E R K I N 3. 3a 3c 3e C A N N I Z Z A R O 4. 4b 4d 4j

  2. A U E X S P N P O I R

  3. A U A E P X S P N P U E R O I S O O E E A R R O O E S S E S C H E N M O S E R 5. 5a 5e 5h 5i 5j P A U S O N – K H A N D 6. 6a 6c 6e 6i REFO R M A T S K Y 7. 7a 7b 7d 7g 7i ROS E N M U N D 8. 8a 8b 8c Synthesis of theestersidechains of somepotentialyantileukemic Harringtoniaalkaloidsfromchiralcitrates R.A. Ancliff, A.T. Russell, A.J. Sanderson Chem. Commun., 2006, 68, 3243-3245

  4. A U A E P X S P N P U E R O I S O O E E A R R O O E S S

  5. A U E I N A E P X S P N A P U E R R O S E I L A S O R O A D E E A T R O O A D E S S T D I E C K M A N N 9. 9a 9c 9g 9i F R I E D L A N D E R 10. 10d 10f 10g 10i 10k IonicLiquid-PromotedRegiospecificFriedlanderAnnulation: Novel Synthesis of Quinolines and FusedPolycyclicQuinolines S. S. Palimkar, S. A. Siddiqui, T. Daniel, R. J. Lahoti, K. V. Srinivasan, J. Org. Chem., 2003, 68, 9371-9378 A C H M A T O W I C Z 11. 11a 11e 11f 11i Design and synthesis of novel tetrahydro-2H-Pyrano[3,2-c]pyridazin-3(6H)-one derivativesas potentialanticanceragents By Al-Tel TalebH. Eur. J. of Med. Chem.2010,45(12), 5724-5731 H A N T Z S C H 12. 12d 12f One-Step Continuous Flow Synthesis of Highly Substituted Pyrrole-3-carboxylic Acid Derivatives via in Situ Hydrolysis of tert-Butyl Esters A. Herath, N.D.P. Cosford Org. Lett., 2010, 12, 5182-5185

  6. A U E I N A E P X S P N A P U E R R O S E I L A S O R O A D E E A T R O O A D E S S T

  7. A U S N R E I N A E P X S P N A P U E R R O S E I E L V A S O E G R O A D M E E I A T R O O L H A D A E S V S T I G A B R I E L 13. 13a 13d 13f 13g H O F MA N N 14. 14a 14d 14e 14g V I L S M E IE R 15. 15a 15d 15h F A V O R S K I I 16. 16c 16h 16i A convenient preparation of 3-isopropyl-1-methylcyclclopentylmethanol and 1-isopropyl-3-methylcyclopentylmethanol via Favorskii rearrangement M. Ambrosini, N. baricordi, S. Benetti, C. de Risi, G.P. Pollini, V. Zanirato Tetrahedron: Asymmetry., 2009, 20, 2145-2148

  8. A U S N R E I N A E P X S P N A P U E R R O S E I E L V A S O E G R O A D M E E I A T R O O L H A D A E S V S T I

  9. C E A U S I N R E C N I N A E P X S P C N A P U E R R A O S E I E L V N A S O E G R A D M E E I A T R O O O L H A D A E N S V A S T I C H I C H I B A B I N 17. 17c 17d 17h 17k A new versatile synthesis of 4-substituted diaminopyridine derivatives S. Banerjee, B. Voit, G. Heinrich, F. Böhme Tetrahedron Lett.,2012, 53, 2236-2238. M A N N I C H 18. 18b 18d 18f TheDirect and Enantioselective, One-Pot, Three-Component, Cross-MannichReaction of AldehydesY. Hayashi, W. Tsuboi, I. Ashimine, T. Urushima, M. Shoji, K. Sakai, Angew. Chem. Int. Ed., 2003, 42, 3677-3680. BE C K M A N N 19. 19b 19c 19h Beckmann Rearrangement of Oximes under Very Mild ConditionsDe Luca, L., Giacomelli, G., Porcheddu, A., J. Org. Chem., 2002, 67, 6272-6274.

  10. C E A U S I N R E C N I N A E P X S P C N A P U E R R A O S E I E L V N A S O E G R A D M E E I A T R O O O L H A D A E N S V A S T I

  11. C E A A E U N S I N R E C N U I N A E P X S P C S N A P U E R U F R A O S E I E M L V N A S O E G R O A D M E E I A T R O O L H A D A E N S V A M S T I F U K U Y A M A 20. 20a 20d 20g Synthesis of diarylketonesviaphosphine-free FukuyamareactionK. Kunchithapatham, C.C. Eichman, J.P. Stambuli Chem. Commun., 2011, 47, 12679-12681 S W E R N 21. 21a 21c 21e New odorlessmethodfortheCorey–Kim and Swernoxidationsutilizingdodecylmethylsulfide (Dod-S-Me)S.-I. Ohsugia, K. Nishidea, K. Oonob, K. Okuyamab, M. Fudesakaa, S. Kodamaa, M. Node, Tetrahedron, 2003, 59, 8393-8398 K U M A D A 22. 22b 22c 22f Nickel-CatalyzedKumada Cross-CouplingReactions of TertiaryAlkylmagnesiumHalidesand ArylBromides/TriflatesA. Joshi-Pangu, C.-Y. Wang, M. R. Biscoe, J. Am. Chem. Soc., 2011, 133, 8478-8481.

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