-
1
-
-
0029010279
-
-
Other related references are cited therein
-
1. For the recent synthesis of (+)-brefeldin A, see: Kim, D; Lim, J. I. Tetrahedron Lett. 1995, 36, 5035. Other related references are cited therein.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 5035
-
-
Kim, D.1
Lim, J.I.2
-
2
-
-
0010501330
-
-
2. a) Kitahara, T.; Mori, K.; Matsui, M. Tetrahedron Lett. 1979, 3021. Kitahara, T.; Mori, K Tetrahedron, 1984, 40, 2935.
-
(1979)
Tetrahedron Lett.
, vol.3021
-
-
Kitahara, T.1
Mori, K.2
Matsui, M.3
-
3
-
-
0021720782
-
-
2. a) Kitahara, T.; Mori, K.; Matsui, M. Tetrahedron Lett. 1979, 3021. Kitahara, T.; Mori, K Tetrahedron, 1984, 40, 2935.
-
(1984)
Tetrahedron
, vol.40
, pp. 2935
-
-
Kitahara, T.1
Mori, K.2
-
5
-
-
0022643696
-
-
c) Trost, B. M.; Lynch, J.; Renaut, P.; Steinman, D. H. J. Am. Chem. Soc. 1986, 108, 284.
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 284
-
-
Trost, B.M.1
Lynch, J.2
Renaut, P.3
Steinman, D.H.4
-
6
-
-
0025880985
-
-
d) Taber, D. F.; Silverberg, L. J.; Robinson, E. D. J. Am. Chem. Soc. 1991, 113, 6639.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 6639
-
-
Taber, D.F.1
Silverberg, L.J.2
Robinson, E.D.3
-
8
-
-
0028349304
-
-
Reference 1 has shown elegant elaboration of hydroxyheptenyl chain of brefeldin A followed by cyclopentane construction
-
f) Miyaoka, H.; Kajiwara, M. J. Chem. Soc. Chem. Commun. 1994, 483. Reference 1 has shown elegant elaboration of hydroxyheptenyl chain of brefeldin A followed by cyclopentane construction.
-
(1994)
J. Chem. Soc. Chem. Commun.
, pp. 483
-
-
Miyaoka, H.1
Kajiwara, M.2
-
9
-
-
0030979211
-
-
3. Suh, Y.-G.; Jung, J.-K.; Kim, S.-A.; Shin, D.-Y.; Min, K.-H. Tetrahedron Lett. 1997, 38, 3911.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 3911
-
-
Suh, Y.-G.1
Jung, J.-K.2
Kim, S.-A.3
Shin, D.-Y.4
Min, K.-H.5
-
10
-
-
0030567357
-
-
4. Tavares, F.; Lawson, J. P.; Meyers, A. I. J. Am. Chem. Soc. 1996, 118, 3303.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 3303
-
-
Tavares, F.1
Lawson, J.P.2
Meyers, A.I.3
-
11
-
-
0000513405
-
-
5. Drian, C. L.; Greene, A. E. J. Am. Chem. Soc. 1982, 104, 5473. Nokami, J.; Ohkura, M.; Dan-Oh, Y.; Sakamoto, Y. Tetrahedron Lett. 1991, 32, 2409. The known 6-silyloxy-1-heptyne (6) was straightforwardly prepared from (S)-lactate in 74 % overall yield by our own six step sequence. (equition presented)
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 5473
-
-
Drian, C.L.1
Greene, A.E.2
-
12
-
-
0025854913
-
-
The known 6-silyloxy-1-heptyne (6) was straightforwardly prepared from (S)-lactate in 74 % overall yield by our own six step sequence. (equition presented)
-
5. Drian, C. L.; Greene, A. E. J. Am. Chem. Soc. 1982, 104, 5473. Nokami, J.; Ohkura, M.; Dan-Oh, Y.; Sakamoto, Y. Tetrahedron Lett. 1991, 32, 2409. The known 6-silyloxy-1-heptyne (6) was straightforwardly prepared from (S)-lactate in 74 % overall yield by our own six step sequence. (equition presented)
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 2409
-
-
Nokami, J.1
Ohkura, M.2
Dan-Oh, Y.3
Sakamoto, Y.4
-
13
-
-
0010500862
-
-
note
-
2, vi) Litium acetylide-EDA complex, DMSO, 81% for 2steps
-
-
-
-
14
-
-
0010420714
-
-
note
-
2).
-
-
-
-
15
-
-
0001164834
-
-
7. Mori, Y.; Kuhara, M,; Takeuchi, A.; Suzuki, M. Tetrahedron Lett. 1988, 29, 5419.
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 5419
-
-
Mori, Y.1
Kuhara, M.2
Takeuchi, A.3
Suzuki, M.4
-
16
-
-
0022896921
-
-
8. Meyers. A. I.; Lawson, J. P.; Walker, D. G.; Linderman, R. J. J. Org. Chem. 1986, 51, 5111.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 5111
-
-
Meyers, A.I.1
Lawson, J.P.2
Walker, D.G.3
Linderman, R.J.4
-
17
-
-
46149140781
-
-
9. Horita, K.; Yoshioka, T.; Tanaka, T.; Oikawa, Y.; Yonemitsu, O. Tetrahedron 1986, 42, 3021.
-
(1986)
Tetrahedron
, vol.42
, pp. 3021
-
-
Horita, K.1
Yoshioka, T.2
Tanaka, T.3
Oikawa, Y.4
Yonemitsu, O.5
-
19
-
-
49549126692
-
-
11. Unpublished results. The details for this extremely mild desulfonylation procedure will be reported soon in due courses. For Trost's conditions, see; Trost, B. M.; Arndt, H. C.; Strege, P. E.; Verhoeven, T. R. Tetrahedron Lett. 1976, 39, 3477.
-
(1976)
Tetrahedron Lett.
, vol.39
, pp. 3477
-
-
Trost, B.M.1
Arndt, H.C.2
Strege, P.E.3
Verhoeven, T.R.4
-
20
-
-
0010421418
-
-
DIBAL reduction of bicyclic lactone 12 provided the hydroxy aldehyde rather than lactol
-
12. DIBAL reduction of bicyclic lactone 12 provided the hydroxy aldehyde rather than lactol.
-
-
-
-
21
-
-
0010503295
-
-
note
-
2).
-
-
-
-
22
-
-
0002339617
-
-
14. Corey, E. J.; Wellenberg, R. H. Tetrahedron Lett. 1976, 4705. Honda, M.; Hirata, K.; Sueoka, H.; Katsuki, T.; Yamaguchi, M. Tetrahedron Lett. 1981, 22, 2679.
-
(1976)
Tetrahedron Lett.
, pp. 4705
-
-
Corey, E.J.1
Wellenberg, R.H.2
-
23
-
-
0019521675
-
-
14. Corey, E. J.; Wellenberg, R. H. Tetrahedron Lett. 1976, 4705. Honda, M.; Hirata, K.; Sueoka, H.; Katsuki, T.; Yamaguchi, M. Tetrahedron Lett. 1981, 22, 2679.
-
(1981)
Tetrahedron Lett.
, vol.22
, pp. 2679
-
-
Honda, M.1
Hirata, K.2
Sueoka, H.3
Katsuki, T.4
Yamaguchi, M.5
|