-
3
-
-
0026448725
-
-
A. Endo, J. Lipid Res., 1992, 33, 1569–1582.
-
(1992)
J. Lipid Res.
, vol.33
, pp. 1569-1582
-
-
Endo, A.1
-
4
-
-
84906786581
-
-
J. Fabris, Z. Časar, I. G. Smilović and M. Črnugelj, Synthesis, 2014, 46, 2333–2346;
-
(2014)
Synthesis
, vol.46
, pp. 2333-2346
-
-
Fabris, J.1
Časar, Z.2
Smilović, I.G.3
Črnugelj, M.4
-
6
-
-
77950791804
-
-
N. Andrushko, V. Andrushko, V. Tararov, A. Korostylev, G. König and A. Börner, Chirality, 2010, 22, 534–541;
-
(2010)
Chirality
, vol.22
, pp. 534-541
-
-
Andrushko, N.1
Andrushko, V.2
Tararov, V.3
Korostylev, A.4
König, G.5
Börner, A.6
-
7
-
-
71849097295
-
-
d), and, WO2010023678
-
S. P. Anegondi, S. Rajmahendra, J. Joseph and P. V. Srinivas, PCT Int. Appl. WO2010023678, 2010;
-
(2010)
PCT Int. Appl.
-
-
Anegondi, S.P.1
Rajmahendra, S.2
Joseph, J.3
Srinivas, P.V.4
-
8
-
-
46049114957
-
-
A. Korostylev, V. Andrushko, N. Andrushko, V. I. Tararov, G. König and A. Börner, Eur. J. Org. Chem., 2008, 840–846;
-
(2008)
Eur. J. Org. Chem.
, pp. 840-846
-
-
Korostylev, A.1
Andrushko, V.2
Andrushko, N.3
Tararov, V.I.4
König, G.5
Börner, A.6
-
9
-
-
34447320746
-
-
J. A. Pfefferkorn, C. Choi, Y. Song, B. K. Trivedi, S. D. Larsen, V. Askew, L. Dillon, J. C. Hanselman, Z. Lin, G. Lu, A. Robertson, C. Sekerke, B. Auerbach, A. Pavlovsky, M. S. Harris, G. Bainbridge and N. Caspers, Bioorg. Med. Chem. Lett., 2007, 17, 4531–4537;
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 4531-4537
-
-
Pfefferkorn, J.A.1
Choi, C.2
Song, Y.3
Trivedi, B.K.4
Larsen, S.D.5
Askew, V.6
Dillon, L.7
Hanselman, J.C.8
Lin, Z.9
Lu, G.10
Robertson, A.11
Sekerke, C.12
Auerbach, B.13
Pavlovsky, A.14
Harris, M.S.15
Bainbridge, G.16
Caspers, N.17
-
10
-
-
34447335377
-
-
M. Acemoglu, A. Brodbeck, A. Garcia, D. Grimier, M. Hassel, B. Riss and R. Schreiber, Helv. Chim. Acta, 2007, 90, 1069–1081;
-
(2007)
Helv. Chim. Acta
, vol.90
, pp. 1069-1081
-
-
Acemoglu, M.1
Brodbeck, A.2
Garcia, A.3
Grimier, D.4
Hassel, M.5
Riss, B.6
Schreiber, R.7
-
11
-
-
84978046723
-
-
S. D. Larsen, Y. Song, K. L. Sun, S. R. Miller and B. K. Trivedi, Tetrahedron, 2007, 63, 8124–8134;
-
(2007)
Tetrahedron
, vol.63
, pp. 8124-8134
-
-
Larsen, S.D.1
Song, Y.2
Sun, K.L.3
Miller, S.R.4
Trivedi, B.K.5
-
13
-
-
12144289185
-
-
T. Hosoya, T. Hiramatsu, T. Ikemoto, M. Nakanishi, H. Aoyama, A. Hosoya, T. Iwata, K. Maruyama, M. Endo and M. Suzuki, Org. Biomol. Chem., 2004, 2, 637–641.
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 637-641
-
-
Hosoya, T.1
Hiramatsu, T.2
Ikemoto, T.3
Nakanishi, M.4
Aoyama, H.5
Hosoya, A.6
Iwata, T.7
Maruyama, K.8
Endo, M.9
Suzuki, M.10
-
14
-
-
77956923491
-
-
S. E. Park, E. H. Nam, H. B. Jang, J. S. Oh, S. Some, Y. S. Lee and C. E. Song, Adv. Synth. Catal., 2010, 352, 2211–2217;
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 2211-2217
-
-
Park, S.E.1
Nam, E.H.2
Jang, H.B.3
Oh, J.S.4
Some, S.5
Lee, Y.S.6
Song, C.E.7
-
15
-
-
77955732976
-
-
b), and, WO2008130638
-
V. K. Kansal, B. P. Chaurasia, H. K. Patel, V. Gothalia and H. Gandhi, PCT Int. Appl. WO2008130638, 2008;
-
(2008)
PCT Int. Appl.
-
-
Kansal, V.K.1
Chaurasia, B.P.2
Patel, H.K.3
Gothalia, V.4
Gandhi, H.5
-
17
-
-
0025824339
-
-
D. S. Karanewsky, M. F. Malley and J. Z. Gougoutas, J. Org. Chem., 1991, 56, 3744–3747;
-
(1991)
J. Org. Chem.
, vol.56
, pp. 3744-3747
-
-
Karanewsky, D.S.1
Malley, M.F.2
Gougoutas, J.Z.3
-
19
-
-
84934968709
-
-
R. Metzner, W. Hummel, F. Wetterich, B. König and H. Gröger, Org. Process Res. Dev., 2015, 19, 635.
-
(2015)
Org. Process Res. Dev.
, vol.19
, pp. 635
-
-
Metzner, R.1
Hummel, W.2
Wetterich, F.3
König, B.4
Gröger, H.5
-
20
-
-
84859604124
-
-
A. Bariotaki, D. Kalaitzakis and I. Smonou, Org. Lett., 2012, 14, 1792–1795;
-
(2012)
Org. Lett.
, vol.14
, pp. 1792-1795
-
-
Bariotaki, A.1
Kalaitzakis, D.2
Smonou, I.3
-
21
-
-
84864974876
-
-
W. Li, W. Fan, X. Ma, X. Tao, X. Li, X. Xie and Z. Zhang, Chem. Commun., 2012, 48, 8976–8978;
-
(2012)
Chem. Commun.
, vol.48
, pp. 8976-8978
-
-
Li, W.1
Fan, W.2
Ma, X.3
Tao, X.4
Li, X.5
Xie, X.6
Zhang, Z.7
-
22
-
-
84859329365
-
-
W. Fan, W. Li, X. Ma, X. Tao, X. Li, Y. Yao, X. Xiea and Z. Zhang, Chem. Commun., 2012, 48, 4247–4249;
-
(2012)
Chem. Commun.
, vol.48
, pp. 4247-4249
-
-
Fan, W.1
Li, W.2
Ma, X.3
Tao, X.4
Li, X.5
Yao, Y.6
Xiea, X.7
Zhang, Z.8
-
23
-
-
46049084988
-
-
V. Andrushko, reN. Andrushko, G. König and A. Börner, Tetrahedron Lett., 2008, 49, 4836–4839;
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 4836-4839
-
-
Andrushko, V.1
Andrushko, N.2
König, G.3
Börner, A.4
-
24
-
-
33745357176
-
-
Z. Guo, Y. Chen, A. Goswami, R. L. Hanson and R. N. Patel, Tetrahedron: Asymmetry, 2006, 17, 1589–1602;
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 1589-1602
-
-
Guo, Z.1
Chen, Y.2
Goswami, A.3
Hanson, R.L.4
Patel, R.N.5
-
26
-
-
33646214176
-
-
a), WO03064382
-
G. P. Chen, P. K. Kapa, E. M. Loeser, U. Beutler, W. Zaugg, M. J. Girgis, PCT Int. Appl. WO03064382, 2003;
-
(2003)
PCT Int. Appl.
-
-
Chen, G.P.1
Kapa, P.K.2
Loeser, E.M.3
Beutler, U.4
Zaugg, W.5
Girgis, M.J.6
-
27
-
-
0034840928
-
-
M. Suzuki, H. Iwasaki, Y. Fujikawa, M. Kitahara, M. Sakashita and R. Sakoda, Bioorg. Med. Chem., 2001, 9, 2727–2743;
-
(2001)
Bioorg. Med. Chem.
, vol.9
, pp. 2727-2743
-
-
Suzuki, M.1
Iwasaki, H.2
Fujikawa, Y.3
Kitahara, M.4
Sakashita, M.5
Sakoda, R.6
-
28
-
-
0033581607
-
-
M. Suzuki, Y. Yanagawa, H. Iwasaki, H. Kanda, K. Yanagihara, H. Matsumoto, Y. Ohara, Y. Yazaki and R. Sakoda, Bioorg. Med. Chem. Lett., 1999, 9, 2977–2982;
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 2977-2982
-
-
Suzuki, M.1
Yanagawa, Y.2
Iwasaki, H.3
Kanda, H.4
Yanagihara, K.5
Matsumoto, H.6
Ohara, Y.7
Yazaki, Y.8
Sakoda, R.9
-
29
-
-
0023105558
-
-
J. E. Lynch, R. P. Volante, R. V. Wattley and I. Shinkai, Tetrahedron Lett., 1987, 28, 1385–1388.
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 1385-1388
-
-
Lynch, J.E.1
Volante, R.P.2
Wattley, R.V.3
Shinkai, I.4
-
31
-
-
85043204895
-
-
b), and, U. S. Patent US2003166946
-
A. Wolleb and H. Wolleb, U. S. Patent US2003166946, 2003;
-
(2003)
-
-
Wolleb, A.1
Wolleb, H.2
-
32
-
-
0030743263
-
-
O. Tempkin, S. Abel, C. P. Chen, R. Underwood, K. Prasad, K. M. Chen, O. Repic and T. J. Blacklock, Tetrahedron, 1997, 53, 10659–10670;
-
(1997)
Tetrahedron
, vol.53
, pp. 10659-10670
-
-
Tempkin, O.1
Abel, S.2
Chen, C.P.3
Underwood, R.4
Prasad, K.5
Chen, K.M.6
Repic, O.7
Blacklock, T.J.8
-
33
-
-
0027145575
-
-
C. Chan, E. J. Bailey, C. D. Hartley, D. F. Hayman, J. L. Hutson, G. G. A. Inglis, P. S. Jones, S. E. Keeling, B. E. Kirk, R. B. Lamont, M. G. Lester, J. M. Pritchard, B. C. Ross, J. J. Scicinski, S. J. Spooner, G. Smith, I. P. Steeples and N. S. Watson, J. Med. Chem., 1993, 36, 3646–3657;
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3646-3657
-
-
Chan, C.1
Bailey, E.J.2
Hartley, C.D.3
Hayman, D.F.4
Hutson, J.L.5
Inglis, G.G.A.6
Jones, P.S.7
Keeling, S.E.8
Kirk, B.E.9
Lamont, R.B.10
Lester, M.G.11
Pritchard, J.M.12
Ross, B.C.13
Scicinski, J.J.14
Spooner, S.J.15
Smith, G.16
Steeples, I.P.17
Watson, N.S.18
-
34
-
-
0027068030
-
-
D. V. Patel, R. J. Schmidt and E. M. Gordon, J. Org. Chem., 1992, 57, 7143–7151.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 7143-7151
-
-
Patel, D.V.1
Schmidt, R.J.2
Gordon, E.M.3
-
35
-
-
85027940172
-
-
S. Tartaggia, C. Ferrari, M. Pontini and O. De Lucchi, Eur. J. Org. Chem., 2015, 4102–4107;
-
(2015)
Eur. J. Org. Chem.
, pp. 4102-4107
-
-
Tartaggia, S.1
Ferrari, C.2
Pontini, M.3
De Lucchi, O.4
-
36
-
-
84962695471
-
-
b), and, WO2014128022
-
O. DeLucchi, S. Tartaggia, C. Ferrari, M. Galvagni, M. Pontini, S. Fogal, R. Motterle, R. M. Moreno and A. Comely, PCT Int. Appl. WO2014128022, 2014
-
(2014)
PCT Int. Appl.
-
-
De Lucchi, O.1
Tartaggia, S.2
Ferrari, C.3
Galvagni, M.4
Pontini, M.5
Fogal, S.6
Motterle, R.7
Moreno, R.M.8
Comely, A.9
-
37
-
-
85043200667
-
-
Acetalization experiments were performed by using ethylene glycol or 1,2-bis(trimethylsiloxy)ethane in toluene or cyclohexane in the presence of several Brønsted and Lewis acid catalysts. However, transesterification of the methyl ester group was the most favored process under the acetalization conditions, However, transesterification of the methyl ester group was the most favored process under the acetalization conditions
-
Acetalization experiments were performed by using ethylene glycol or 1,2-bis(trimethylsiloxy)ethane in toluene or cyclohexane in the presence of several Brønsted and Lewis acid catalysts. However, transesterification of the methyl ester group was the most favored process under the acetalization conditions
-
-
-
-
38
-
-
0037006786
-
-
K. M. Cheung, S. J. Coles, M. B. Hursthouse, N. I. Johnson and P. M. Jordan, Angew. Chem. Int. Ed., 2002, 41, 1198–1202;
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 1198-1202
-
-
Cheung, K.M.1
Coles, S.J.2
Hursthouse, M.B.3
Johnson, N.I.4
Jordan, P.M.5
-
39
-
-
84977967573
-
-
Angew. Chem., 2002, 114, 1246–1250.
-
(2002)
Angew. Chem.
, vol.114
, pp. 1246-1250
-
-
-
41
-
-
29144494500
-
-
Angew. Chem., 2005, 117, 366–369.
-
(2005)
Angew. Chem.
, vol.117
, pp. 366-369
-
-
-
42
-
-
77149155653
-
-
S. K. Ma, J. Gruber, C. Davis, L. Newman, D. Gray, A. Wang, J. Grate, G. W. Huisman and R. A. Sheldon, Green Chem., 2010, 12, 81–86.
-
(2010)
Green Chem.
, vol.12
, pp. 81-86
-
-
Ma, S.K.1
Gruber, J.2
Davis, C.3
Newman, L.4
Gray, D.5
Wang, A.6
Grate, J.7
Huisman, G.W.8
Sheldon, R.A.9
-
43
-
-
77149176912
-
-
J. Liang, E. Mundorff, R. Voldari, S. Jenne, L. Gilson, A. Conway, A. Krebber, J. Wong, G. Huisman, S. Truesdell and J. Lalonde, Org. Process Res. Dev., 2010, 14, 188–192;
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 188-192
-
-
Liang, J.1
Mundorff, E.2
Voldari, R.3
Jenne, S.4
Gilson, L.5
Conway, A.6
Krebber, A.7
Wong, J.8
Huisman, G.9
Truesdell, S.10
Lalonde, J.11
-
44
-
-
58349117440
-
-
L. Wei, T. Makowski, C. Martinez and A. Ghosh, Tetrahedron: Asymmetry, 2008, 19, 2648–2651.
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 2648-2651
-
-
Wei, L.1
Makowski, T.2
Martinez, C.3
Ghosh, A.4
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