2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a.

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2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k

2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k b 1g 2. 2a 2e 2f 3. 3a 3c 3e 4. 4b 4d 4j O X I C O P E- X E S U P S K R A U P P E R K I N P R I C A N N I Z Z A R O A N O Efficient microwave-assisted synthesis of quinolines and Dihydroquinolines under solvent-free conditions B. C. Ranu, A. Hajra, S.S. Dey, U. Jana J. Org. Chem., 2003, 59,

2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O

5. 5a 5e 5h 5i 5j 7. 7a 7b 7d 7g 7i 2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O E S C H E N M O S E R E E E O S P A U O R E F O R M A T S K Y R O S E N M U N D R O S 6. 6a 6c 6e 6i P A U S O N – K H A N D E O A S R 8. 8a 8b 8c Synthesis of the ester side chains of some potentialy antileukemic Harringtonia alkaloids from chiral citrates R.A. Ancliff, A.T. Russell, A.J. Sanderson Chem. Commun., 2006, 68,

2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O E E E O S P A U O R O S E O A S R

9. 9a 9c 9g 9i d 10f 10g 10i 10k a 11e 11f 11i Ionic Liquid-Promoted Regiospecific Friedlander Annulation: Novel Synthesis of Quinolines and Fused Polycyclic Quinolines S. S. Palimkar, S. A. Siddiqui, T. Daniel, R. J. Lahoti, K. V. Srinivasan, J. Org. Chem., 2003, 68, d 12f 2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O E E E O S R P A U O E O A S R O S D I E C K M A N N D E A N A C H M A T O W I C Z A A T I F R I E D L A N D E R E L A D R H A N T Z S C H T S Design and synthesis of novel tetrahydro-2H-Pyrano[3,2-c]pyridazin-3(6H)-one derivatives as potential anticancer agents By Al-Tel Taleb H. Eur. J. of Med. Chem. 2010, 45(12), 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,

2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O E E E O S R P A U O E O A S R O S D E A N A A T I E L A D R T S

15. 15a 15d 15h c 16h 16i a 13d 13f 13g a 14d 14e 14g 2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O E E E O S R P A U O E O A S R O S D E A N A A T I E L A D R T S G A B R I E L G R E L H O F M A N N H M A N V I L S M E I E R V S E F A V O R S K I I V I I 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,

2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O E E E O S R P A U O E O A S R O S D E A N A A T I E L A D R T S G R E L H M A N V S E V I I

17. 17c 17d 17h 17k b 18d 18f b 19c 19h Beckmann Rearrangement of Oximes under Very Mild Conditions De Luca, L., Giacomelli, G., Porcheddu, A., J. Org. Chem., 2002, 67, e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O E E E O S R P A U O E O A S R O S D E A N A A T I E L A D R T S G R E L H M A N V S E V I I C H I C H I B A B I N I C A N M A N N I C H A N C B E C K M A N N E C N A new versatile synthesis of 4-substituted diaminopyridine derivatives S. Banerjee, B. Voit, G. Heinrich, F. Böhme Tetrahedron Lett., 2012, 53, The Direct and Enantioselective, One-Pot, Three-Component, Cross-Mannich Reaction of Aldehydes Y. Hayashi, W. Tsuboi, I. Ashimine, T. Urushima, M. Shoji, K. Sakai, Angew. Chem. Int. Ed., 2003, 42,

2e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O E E E O S R P A U O E O A S R O S D E A N A A T I E L A D R T S G R E L H M A N V S E V I I I C A N A N C E C N

20. 20a 20d 20g a 21c 21e b 22c 22f Nickel-Catalyzed Kumada Cross-Coupling Reactions of Tertiary Alkylmagnesium Halides and Aryl Bromides/Triflates A. Joshi-Pangu, C.-Y. Wang, M. R. Biscoe, J. Am. Chem. Soc., 2011, 133, New odorless method for the Corey–Kim and Swern oxidations utilizing dodecyl methyl sulfide (Dod-S-Me) S.-I. Ohsugia, K. Nishidea, K. Oonob, K. Okuyamab, M. Fudesakaa, S. Kodamaa, M. Node, Tetrahedron, 2003, 59, e 14g 6i 21c 1b 6a 19b 13d 17c 9c 21e 17d 11i 4b 18d 20d 9i 18f 22f 1g 15d 6c 4d 20a 8a 17h 19c 11e 21a 4j 2f 22b 10d 2a 12f 3e 15h 22c 3a 10k 5j 15a 16i 7b 19h 13f 10g 10i 5e 14d 6e 5i 11f 7a 9g 3c 7g 10f 13a 8b. 12d 14a 5h 20g 11a 7i 18b 13g 16c 14e 5a 9a 16h 8c 7d 17k X E S U P P R I A N O E E E O S R P A U O E O A S R O S D E A N A A T I E L A D R T S G R E L H M A N V S E V I I I C A N A N C E C N F U K U Y A M A F U M S W E R N S E N U M A K U M A D A Synthesis of diaryl ketones via phosphine-free Fukuyama reaction K. Kunchithapatham, C.C. Eichman, J.P. Stambuli Chem. Commun., 2011, 47,