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2. 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 - 1. 1b 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, 813-819

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4. 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, 3243-3245

5. 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

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7. 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

8. 15. 15a 15d 15h 16. 16c 16h 16i 13. 13a 13d 13f 13g 14. 14a 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, 2145-2148

9. 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

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