41. Garcia I, Pe ´rez M, Gomez G, Fall Y (2008) Tetrahedron Lett 49(8):1344–1347
42. Grant TN, Benson CL, West FG (2008) Org Lett 10(18):3985–3988
43. Paduraru MP, Wilson PD (2003) Org Lett 5(25):4911–4913
44. Reddy CR, Ramesh P, Rao NN, Ali SA (2011) Eur J Org Chem (11): 2133–2141
45. Purino MA, Ramirez MA, Daranas AH, Martin VS, Padron JI (2012) Org Lett 14
(23):5904–5907
46. Yadav JS, Reddy BVS, Yadav NN, Satheesh G (2008) Synthesis (17): 2733–2738
47. Castaldi MP, Troast DM, Porco JA Jr (2009) Org Lett 11(15):3362–3365
48. O’Neil KE, Kingree SV, Minbiole KPC (2005) Org Lett 7(3):515–517
49. Crisostomo FRP, Martin T, Martin VS (2004) Org Lett 6(4):565–568
50. Yamamoto Y, Yamada J-I, Kadota I (1991) Tetrahedron Lett 32(48):7069–7072
51. Kuranaga T, Ohtani N, Tsutsumi R, Baden DG, Wright JLC, Satake M, Tachibana K (2011)
Org Lett 13(4):696–699
52. Kadota I, Abe T, Ishitsuka Y, Touchy AS, Nagata R, Yamamoto Y (2007) Tetrahedron Lett
48(2):219–221
53. Taillier C, Gille B, Bellosta V, Cossy J (2005) J Org Chem 70(6):2097–2108
54. Fleck M, Bach T (2010) Chem Eur J 16(20):6015–6032
55. Lemaire P, Balme G, Desbordes P, Vors J-P (2003) Org Biomol Chem 1(23):4209–4219
56. Martin DBC, Vanderwal CD (2011) Chem Sci 2(4):649–651
57. Jepsen TH, Larsen M, Jorgensen M, Bronsted Nielsen M (2012) Synlett 23(3):418–422
58. Nishimura K, Kinugawa M (2012) Org Process Res Dev 16(2):225–231
59. Bosch J, Bachs J, Gomez AM, Griera R, Ecija M, Amat M (2012) J Org Chem 77
(14):6340–6344
60. Jones SB, Simmons B, Mastracchio A, MacMillan DWC (2011) Nature 475(7355):183–188
61. Lautens M, Paquin JF, Piguel S (2002) J Org Chem 67(11):3972–3974
62. Yoshida H, Asatsu Y, Mimura Y, Ito Y, Ohshita J, Takaki K (2011) Angew Chem Int Ed 50
(41):9676–9679
63. Parthasarathy K, Han H, Prakash C, Cheng C-H (2012) Chem Commun 48(52):6580–6582
64. Alcaide B, Almendros P, Martinez del Campo T (2007) Angew Chem Int Ed 46
(35):6684–6687
65. Rainier JD (2010) Synthesis of natural products containing medium-size oxygen heterocycles
by ring-closing alkene metathesis. In: Cossy J, Arseniyadis S, Meyer C (eds) Metathesis in
natural product synthesis: strategies, substrates and catalysts. Wiley-VCH, Weinheim
66. Crimmins MT, DeBaillie AC (2003) Org Lett 5(17):3009–3011
67. Bruder M, Haseler PL, Muscarella M, Lewis W, Moody CJ (2010) J Org Chem 75
(2):353–358
68. Chang M-Y, Wu M-H, Lee T-W (2012) Tetrahedron 68(31):6224–6230
69. Chang M-Y, Lee N-C (2012) Synlett 23(6):867–872
70. Doveston RG, Steendam R, Jones S, Taylor RJK (2012) Org Lett 14(4):1122–1125
71. Gross U, Nieger M, Bra ¨se S (2010) Chem Eur J 16(38):11624–11631
72. He H, Ye K-Y, Wu Q-F, Dai L-X, You S-L (2012) Adv Synth Catal 354(6):1084–1094
73. Schmidt B, Biernat A (2008) Org Lett 10(1):105–108
74. Basu S, Ellinger B, Rizzo S, Deraeve C, Schu ¨rmann M, Preut H, Arndt H-D, Waldmann H
(2011) Proc Natl Acad Sci USA 108(17):6805–6810
75. Shing TKM, Zhong Y-L (2006) Synlett (8): 1205–1208
76. Chatterjee A, Bhattacharya PK (2006) J Org Chem 71(1):345–348
77. Hofmann B, Reissig H-U (1993) Synlett (1): 27–29
78. Leyhane AJ, Snapper ML (2006) Org Lett 8(23):5183–5186
79. Sasaki M, Noguchi T, Tachibana K (1999) Tetrahedron Lett 40(7):1337–1340
80. Lee S-H, Van HTM, Yang SH, Lee K-T, Kwon Y, Cho W-J (2009) Bioorg Med Chem Lett 19
(9):2444–2447
81. Cong Z, Miki T, Urakawa O, Nishino H (2009) J Org Chem 74(10):3978–3981
82. Corser DA, Marples BA, Dart RK (1992) Synlett (12): 987–989
Synthesis of Seven-Membered Ring Ethers and Lactones
319
42. Grant TN, Benson CL, West FG (2008) Org Lett 10(18):3985–3988
43. Paduraru MP, Wilson PD (2003) Org Lett 5(25):4911–4913
44. Reddy CR, Ramesh P, Rao NN, Ali SA (2011) Eur J Org Chem (11): 2133–2141
45. Purino MA, Ramirez MA, Daranas AH, Martin VS, Padron JI (2012) Org Lett 14
(23):5904–5907
46. Yadav JS, Reddy BVS, Yadav NN, Satheesh G (2008) Synthesis (17): 2733–2738
47. Castaldi MP, Troast DM, Porco JA Jr (2009) Org Lett 11(15):3362–3365
48. O’Neil KE, Kingree SV, Minbiole KPC (2005) Org Lett 7(3):515–517
49. Crisostomo FRP, Martin T, Martin VS (2004) Org Lett 6(4):565–568
50. Yamamoto Y, Yamada J-I, Kadota I (1991) Tetrahedron Lett 32(48):7069–7072
51. Kuranaga T, Ohtani N, Tsutsumi R, Baden DG, Wright JLC, Satake M, Tachibana K (2011)
Org Lett 13(4):696–699
52. Kadota I, Abe T, Ishitsuka Y, Touchy AS, Nagata R, Yamamoto Y (2007) Tetrahedron Lett
48(2):219–221
53. Taillier C, Gille B, Bellosta V, Cossy J (2005) J Org Chem 70(6):2097–2108
54. Fleck M, Bach T (2010) Chem Eur J 16(20):6015–6032
55. Lemaire P, Balme G, Desbordes P, Vors J-P (2003) Org Biomol Chem 1(23):4209–4219
56. Martin DBC, Vanderwal CD (2011) Chem Sci 2(4):649–651
57. Jepsen TH, Larsen M, Jorgensen M, Bronsted Nielsen M (2012) Synlett 23(3):418–422
58. Nishimura K, Kinugawa M (2012) Org Process Res Dev 16(2):225–231
59. Bosch J, Bachs J, Gomez AM, Griera R, Ecija M, Amat M (2012) J Org Chem 77
(14):6340–6344
60. Jones SB, Simmons B, Mastracchio A, MacMillan DWC (2011) Nature 475(7355):183–188
61. Lautens M, Paquin JF, Piguel S (2002) J Org Chem 67(11):3972–3974
62. Yoshida H, Asatsu Y, Mimura Y, Ito Y, Ohshita J, Takaki K (2011) Angew Chem Int Ed 50
(41):9676–9679
63. Parthasarathy K, Han H, Prakash C, Cheng C-H (2012) Chem Commun 48(52):6580–6582
64. Alcaide B, Almendros P, Martinez del Campo T (2007) Angew Chem Int Ed 46
(35):6684–6687
65. Rainier JD (2010) Synthesis of natural products containing medium-size oxygen heterocycles
by ring-closing alkene metathesis. In: Cossy J, Arseniyadis S, Meyer C (eds) Metathesis in
natural product synthesis: strategies, substrates and catalysts. Wiley-VCH, Weinheim
66. Crimmins MT, DeBaillie AC (2003) Org Lett 5(17):3009–3011
67. Bruder M, Haseler PL, Muscarella M, Lewis W, Moody CJ (2010) J Org Chem 75
(2):353–358
68. Chang M-Y, Wu M-H, Lee T-W (2012) Tetrahedron 68(31):6224–6230
69. Chang M-Y, Lee N-C (2012) Synlett 23(6):867–872
70. Doveston RG, Steendam R, Jones S, Taylor RJK (2012) Org Lett 14(4):1122–1125
71. Gross U, Nieger M, Bra ¨se S (2010) Chem Eur J 16(38):11624–11631
72. He H, Ye K-Y, Wu Q-F, Dai L-X, You S-L (2012) Adv Synth Catal 354(6):1084–1094
73. Schmidt B, Biernat A (2008) Org Lett 10(1):105–108
74. Basu S, Ellinger B, Rizzo S, Deraeve C, Schu ¨rmann M, Preut H, Arndt H-D, Waldmann H
(2011) Proc Natl Acad Sci USA 108(17):6805–6810
75. Shing TKM, Zhong Y-L (2006) Synlett (8): 1205–1208
76. Chatterjee A, Bhattacharya PK (2006) J Org Chem 71(1):345–348
77. Hofmann B, Reissig H-U (1993) Synlett (1): 27–29
78. Leyhane AJ, Snapper ML (2006) Org Lett 8(23):5183–5186
79. Sasaki M, Noguchi T, Tachibana K (1999) Tetrahedron Lett 40(7):1337–1340
80. Lee S-H, Van HTM, Yang SH, Lee K-T, Kwon Y, Cho W-J (2009) Bioorg Med Chem Lett 19
(9):2444–2447
81. Cong Z, Miki T, Urakawa O, Nishino H (2009) J Org Chem 74(10):3978–3981
82. Corser DA, Marples BA, Dart RK (1992) Synlett (12): 987–989
Synthesis of Seven-Membered Ring Ethers and Lactones
319