3. Kleinke AS, Webb D, Jamison TF (2012) Tetrahedron 68(35):6999–7018
4. Riley DL, van Otterlo WAL (2011) Oxepins and azepines. In: Majumdar KC, Chattopadhay
SK (eds) Heterocycles in natural product synthesis. Wiley, Weinheim, pp 537–565
5. Nicolaou KC, Aversa RJ (2011) Isr J Chem 51(3–4):359–377
6. Nicolaou KC, Frederick MO, Aversa RJ (2008) Angew Chem Int Ed 47(38):7182–7225
7. Hewitt RJ, Harvey JE (2010) J Org Chem 75(3):955–958
8. Dey S, Jayaraman N (2012) Beilstein J Org Chem 8:522–527
9. Sugita Y, Kimura C, Hosoya H, Yamadoi S, Yokoe I (2001) Tetrahedron Lett 42
(6):1095–1098
10. Batchelor R, Harvey JE, Northcote PT, Teesdale-Spittle P, Hoberg JO (2009) J Org Chem 74
(20):7627–7632
11. Furuta H, Hasegawa Y, Mori Y (2009) Org Lett 11(19):4382–4385
12. Furuta H, Hasegawa Y, Hase M, Mori Y (2010) Chem Eur J 16(25):7586–7595
13. Inagaki T, Nakamura Y, Sawaguchi M, Yoneda N, Ayuba S, Hara S (2003) Tetrahedron Lett
44(21):4117–4119
14. Abo T, Sawaguchi M, Senboku H, Hara S (2005) Molecules 10:183–189
15. Raju BC, Saidachary G, Saidachary G, Kumar JA (2012) Tetrahedron 68(31):6289–6297
16. Roux L, Charrier C, Salomon E, Ilhan M, Bisseret P, Tarnus C (2011) Tetrahedron Lett 52
(20):2586–2889
17. Pavlik C, Onorato A, Castro S, Morton M, Peczuh M, Smith MB (2009) Org Lett 11
(16):3722–3725
18. Raghavan S, Babu VS (2011) Chem Eur J 17(30):8487–8494
19. Yus M, Soler T, Foubelo F (2002) Tetrahedron 58(35):7009–7016
20. Lillo VJ, Gomez C, Yus M (2009) Tetrahedron Lett 50(19):2266–2269
21. Singh SA, Kabiraj S, Khandare RP, Nalawade SP, Upar KB, Bhat SV (2009) Synth Commun
40(1):74–80
22. Brunel Y, Rousseau G (1996) J Org Chem 61(17):5793–5800
23. Codelli JA, Puchlopek ALA, Reisman SE (2012) J Am Chem Soc 134(4):1930–1933
24. Alcazar E, Pletcher JM, McDonald FE (2004) Org Lett 6(21):3877–3880
25. Koo B, McDonald FE (2007) Org Lett 9(9):1737–1740
26. Matsumura R, Suzuki T, Sato K, Oku K-i, Hagiwara H, Hoshi T, Ando M, Kamat VP (2000)
Tetrahedron Lett 41(40):7701–7704
27. Matsumura R, Suzuki T, Hagiwara H, Hoshi T, Ando M (2001) Tetrahedron Lett 42
(8):1543–1546
28. McDonald FE, Wang X, Do B, Hardcastle KI (2000) Org Lett 2(18):2917–2919
29. McDonald FE, Bravo F, Wang X, Wei X, Toganoh M, Rodriguez JR, Do B, Neiwert WA,
Hardcastle KI (2002) J Org Chem 67(8):2515–2523
30. Bravo F, McDonald FE, Neiwert WA, Hardcastle KI (2004) Org Lett 6(24):4487–4489
31. Piccialli V, Borbone N, Oliviero G (2007) Tetrahedron Lett 48(29):5131–5135
32. Nicolaou KC, Hwang C-K, Duggan ME, Nugiel DA, Abe Y, Reddy KB, DeFrees SA, Reddy
DR, Awartani RA, Conley SR, Rutjes FPJT, Theodorakis EA (1995) J Am Chem Soc 117
(41):10227–10238
33. Tripathi D, Kumar P (2008) Tetrahedron Lett 49(49):7012–7014
34. Tripathi D, Pandey SK, Kumar P (2009) Tetrahedron 65(11):2226–2231
35. Carren ˜o MM, Des Mazery R, Urbano A, Colobert F, Solladie ´ G (2004) Org Lett 6
(2):297–299
36. Lin J, Zhang W, Jiang N, Niu Z, Bao K, Zhang L, Liu D, Pan C, Yao X (2008) J Nat Prod 71
(11):1938–1941
37. Wang Y, Chen Y, He Q, Xie Y, Yang C (2013) Helv Chim Acta 96(2):296–308
38. Choi YL, Lim HS, Lim HJ, Heo J-N (2012) Org Lett 14(19):5102–5105
39. Sun LL, Hu BL, Tang R-Y, Deng C-L, Zhang X-G (2013) Adv Synth Catal 355
(2–3):377–382
40. Canoa P, Pe ´rez M, Covela B, Gomez G, Fall Y (2007) Tetrahedron Lett 48(19):3441–3443
318
O. Piva
4. Riley DL, van Otterlo WAL (2011) Oxepins and azepines. In: Majumdar KC, Chattopadhay
SK (eds) Heterocycles in natural product synthesis. Wiley, Weinheim, pp 537–565
5. Nicolaou KC, Aversa RJ (2011) Isr J Chem 51(3–4):359–377
6. Nicolaou KC, Frederick MO, Aversa RJ (2008) Angew Chem Int Ed 47(38):7182–7225
7. Hewitt RJ, Harvey JE (2010) J Org Chem 75(3):955–958
8. Dey S, Jayaraman N (2012) Beilstein J Org Chem 8:522–527
9. Sugita Y, Kimura C, Hosoya H, Yamadoi S, Yokoe I (2001) Tetrahedron Lett 42
(6):1095–1098
10. Batchelor R, Harvey JE, Northcote PT, Teesdale-Spittle P, Hoberg JO (2009) J Org Chem 74
(20):7627–7632
11. Furuta H, Hasegawa Y, Mori Y (2009) Org Lett 11(19):4382–4385
12. Furuta H, Hasegawa Y, Hase M, Mori Y (2010) Chem Eur J 16(25):7586–7595
13. Inagaki T, Nakamura Y, Sawaguchi M, Yoneda N, Ayuba S, Hara S (2003) Tetrahedron Lett
44(21):4117–4119
14. Abo T, Sawaguchi M, Senboku H, Hara S (2005) Molecules 10:183–189
15. Raju BC, Saidachary G, Saidachary G, Kumar JA (2012) Tetrahedron 68(31):6289–6297
16. Roux L, Charrier C, Salomon E, Ilhan M, Bisseret P, Tarnus C (2011) Tetrahedron Lett 52
(20):2586–2889
17. Pavlik C, Onorato A, Castro S, Morton M, Peczuh M, Smith MB (2009) Org Lett 11
(16):3722–3725
18. Raghavan S, Babu VS (2011) Chem Eur J 17(30):8487–8494
19. Yus M, Soler T, Foubelo F (2002) Tetrahedron 58(35):7009–7016
20. Lillo VJ, Gomez C, Yus M (2009) Tetrahedron Lett 50(19):2266–2269
21. Singh SA, Kabiraj S, Khandare RP, Nalawade SP, Upar KB, Bhat SV (2009) Synth Commun
40(1):74–80
22. Brunel Y, Rousseau G (1996) J Org Chem 61(17):5793–5800
23. Codelli JA, Puchlopek ALA, Reisman SE (2012) J Am Chem Soc 134(4):1930–1933
24. Alcazar E, Pletcher JM, McDonald FE (2004) Org Lett 6(21):3877–3880
25. Koo B, McDonald FE (2007) Org Lett 9(9):1737–1740
26. Matsumura R, Suzuki T, Sato K, Oku K-i, Hagiwara H, Hoshi T, Ando M, Kamat VP (2000)
Tetrahedron Lett 41(40):7701–7704
27. Matsumura R, Suzuki T, Hagiwara H, Hoshi T, Ando M (2001) Tetrahedron Lett 42
(8):1543–1546
28. McDonald FE, Wang X, Do B, Hardcastle KI (2000) Org Lett 2(18):2917–2919
29. McDonald FE, Bravo F, Wang X, Wei X, Toganoh M, Rodriguez JR, Do B, Neiwert WA,
Hardcastle KI (2002) J Org Chem 67(8):2515–2523
30. Bravo F, McDonald FE, Neiwert WA, Hardcastle KI (2004) Org Lett 6(24):4487–4489
31. Piccialli V, Borbone N, Oliviero G (2007) Tetrahedron Lett 48(29):5131–5135
32. Nicolaou KC, Hwang C-K, Duggan ME, Nugiel DA, Abe Y, Reddy KB, DeFrees SA, Reddy
DR, Awartani RA, Conley SR, Rutjes FPJT, Theodorakis EA (1995) J Am Chem Soc 117
(41):10227–10238
33. Tripathi D, Kumar P (2008) Tetrahedron Lett 49(49):7012–7014
34. Tripathi D, Pandey SK, Kumar P (2009) Tetrahedron 65(11):2226–2231
35. Carren ˜o MM, Des Mazery R, Urbano A, Colobert F, Solladie ´ G (2004) Org Lett 6
(2):297–299
36. Lin J, Zhang W, Jiang N, Niu Z, Bao K, Zhang L, Liu D, Pan C, Yao X (2008) J Nat Prod 71
(11):1938–1941
37. Wang Y, Chen Y, He Q, Xie Y, Yang C (2013) Helv Chim Acta 96(2):296–308
38. Choi YL, Lim HS, Lim HJ, Heo J-N (2012) Org Lett 14(19):5102–5105
39. Sun LL, Hu BL, Tang R-Y, Deng C-L, Zhang X-G (2013) Adv Synth Catal 355
(2–3):377–382
40. Canoa P, Pe ´rez M, Covela B, Gomez G, Fall Y (2007) Tetrahedron Lett 48(19):3441–3443
318
O. Piva