-
1
-
-
0034898137
-
-
(a) Kurosawa, K.; Takahashi, K.; Tsuda, E. J. Antibiot. 2001, 54, 541.
-
(2001)
J. Antibiot.
, vol.54
, pp. 541
-
-
Kurosawa, K.1
Takahashi, K.2
Tsuda, E.3
-
2
-
-
0034904357
-
-
(b) Takahashi, K.; Tsuda, E.; Kurosawa, K. J. Antibiot. 2001, 54, 548.
-
(2001)
J. Antibiot.
, vol.54
, pp. 548
-
-
Takahashi, K.1
Tsuda, E.2
Kurosawa, K.3
-
3
-
-
0036171669
-
-
Kurosawa, K.; Takahashi, K.; Fujise, N.; Yamashita, Y.; Washida, N.; Tsuda, E. J. Antibiot. 2002, 55, 71.
-
(2002)
J. Antibiot.
, vol.55
, pp. 71
-
-
Kurosawa, K.1
Takahashi, K.2
Fujise, N.3
Yamashita, Y.4
Washida, N.5
Tsuda, E.6
-
4
-
-
0035206547
-
-
Kurosawa, K.; Takahashi, K.; Tsuda, E.; Tomida, A.; Tsuruo, T. Jpn. J. Cancer Res. 2001, 92, 1235.
-
(2001)
Jpn. J. Cancer Res.
, vol.92
, pp. 1235
-
-
Kurosawa, K.1
Takahashi, K.2
Tsuda, E.3
Tomida, A.4
Tsuruo, T.5
-
5
-
-
0001009352
-
-
Kakinuma, K.; Hanson, C. A.; Rinehart, K. L., Jr. Tetrahedron 1976, 32, 217. To the best of our knowledge, this interesting antibiotic has not yet been synthesized.
-
(1976)
Tetrahedron
, vol.32
, pp. 217
-
-
Kakinuma, K.1
Hanson, C.A.2
Rinehart K.L., Jr.3
-
6
-
-
0013828097
-
-
(a) Kawai, S.; Kobayashi, K.; Oshima, T.; Egami, F. Arch. Biochem. Biophys. 1965, 112, 537.
-
(1965)
Arch. Biochem. Biophys.
, vol.112
, pp. 537
-
-
Kawai, S.1
Kobayashi, K.2
Oshima, T.3
Egami, F.4
-
7
-
-
0042548716
-
-
(b) Yamazaki, M.; Katoh, F.; Ohishi, J. I.; Koyama, Y. Tetrahedron Lett. 1972, 26, 2701.
-
(1972)
Tetrahedron Lett.
, vol.26
, pp. 2701
-
-
Yamazaki, M.1
Katoh, F.2
Ohishi, J.I.3
Koyama, Y.4
-
8
-
-
0000249280
-
-
and references therein
-
Banfield, J. E.; Black, D. St. C.; Johns, S. R.; Willing, R. I. Aust. J. Chem. 1982, 35, 2247 and references therein.
-
(1982)
Aust. J. Chem.
, vol.35
, pp. 2247
-
-
Banfield, J.E.1
Black, D.St.C.2
Johns, S.R.3
Willing, R.I.4
-
9
-
-
0004220870
-
-
VCH: Weinheim, and references therein
-
(a) Nicolaou, K. C.; Sorensen, E. J. In Classics in Total Synthesis; VCH: Weinheim, 1996; p 265 and references therein. For a similar electrocyclization cascade, see:
-
(1996)
Classics in Total Synthesis
, pp. 265
-
-
Nicolaou, K.C.1
Sorensen, E.J.2
-
10
-
-
0025915671
-
-
(b) Vogt, P.; Schlageter, M.; Widmer, E. Tetrahedron Lett. 1991, 32, 4115.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 4115
-
-
Vogt, P.1
Schlageter, M.2
Widmer, E.3
-
12
-
-
0000575609
-
-
Obtained in one step from p-nitrobenzaldehyde and propionaldehyde: Hirata, Y.; Nakata, H.; Yamada, K.; Okuhara, K.; Naito, T. Tetrahedron 1961, 14, 252.
-
(1961)
Tetrahedron
, vol.14
, pp. 252
-
-
Hirata, Y.1
Nakata, H.2
Yamada, K.3
Okuhara, K.4
Naito, T.5
-
13
-
-
0042548715
-
-
note
-
The stereochemistry of the major isomers 5, 7, 16, and 20 was elucidated by NOESY experiments and in some cases indirectly confirmed by X-ray structure analysis of compounds 10 and 13 (see Supporting Information). Similarly, the syn stereochemistry of aldol 12 was validated by the structure of 13.
-
-
-
-
15
-
-
0001532891
-
-
(b) Boeckman, R. K. Jr.; Pengcheng, S.; Mullins, J. J. Org. Synth. 1999, 77, 141.
-
(1999)
J. Org. Synth.
, vol.77
, pp. 141
-
-
Boeckman R.K., Jr.1
Pengcheng, S.2
Mullins, J.3
-
17
-
-
0005927219
-
-
Scheffold, R., Ed.; VCH: Weinheim, and references therein
-
Heathcock, C. H. In Modern Synthetic Methods; Scheffold, R., Ed.; VCH: Weinheim, 1992; pp 1-102 and references therein.
-
(1992)
Modern Synthetic Methods
, pp. 1-102
-
-
Heathcock, C.H.1
-
19
-
-
0027050190
-
-
(b) Evans, D. A.; Gage, J. R.; Leighton, J. L. J. Am. Chem. Soc. 1992, 114, 9434.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 9434
-
-
Evans, D.A.1
Gage, J.R.2
Leighton, J.L.3
-
20
-
-
0027383856
-
-
(a) Lee, K.; Jackson, J. A.; Wiemer, D. F. J. Org. Chem. 1993, 58, 5967.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 5967
-
-
Lee, K.1
Jackson, J.A.2
Wiemer, D.F.3
-
22
-
-
0023785976
-
-
Nicolaou, K. C.; Daines, R. A.; Chakraborty, T. K.; Ogawa, Y. J. Am. Chem. Soc. 1988, 110, 4685.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 4685
-
-
Nicolaou, K.C.1
Daines, R.A.2
Chakraborty, T.K.3
Ogawa, Y.4
-
23
-
-
0009861937
-
-
Burgess, E. M.; Penton, H. R.; Taylor, E. A. J. Org. Chem. 1973, 58, 26.
-
(1973)
J. Org. Chem.
, vol.58
, pp. 26
-
-
Burgess, E.M.1
Penton, H.R.2
Taylor, E.A.3
-
24
-
-
0029003845
-
-
(a) Knight, S. D.; Overman, L. E.; Pairaudeau, G. J. Am. Chem. Soc. 1995, 117, 5776.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 5776
-
-
Knight, S.D.1
Overman, L.E.2
Pairaudeau, G.3
-
28
-
-
0028340367
-
-
(b) Chen, J.; Wang, T.; Zhao, K. Tetrahedron Lett. 1994, 35, 2827.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 2827
-
-
Chen, J.1
Wang, T.2
Zhao, K.3
-
29
-
-
0001568862
-
-
(a) Duboudin, J. G.; Jousseaume, B.; Bonakdar, A. J. Organomet. Chem. 1979, 168, 227.
-
(1979)
J. Organomet. Chem.
, vol.168
, pp. 227
-
-
Duboudin, J.G.1
Jousseaume, B.2
Bonakdar, A.3
-
31
-
-
0001118624
-
-
Barrett, A. G. M.; Hamprecht, D.; Ohkubo, M. J. Org. Chem. 1997, 62, 9376.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 9376
-
-
Barrett, A.G.M.1
Hamprecht, D.2
Ohkubo, M.3
-
32
-
-
0043049621
-
-
note
-
Unfortunately, all attempts to effect an analogous condensation with phosphonolactone 15 were unsuccessful because of the instability of (Z)-3-iodomethacrolein under the reaction conditions.
-
-
-
-
33
-
-
0035961039
-
-
(a) Vanderwal, C. D.; Vosburg, D. A.; Sorensen, E. J. Org. Lett. 2001, 3, 4307.
-
(2001)
Org. Lett.
, vol.3
, pp. 4307
-
-
Vanderwal, C.D.1
Vosburg, D.A.2
Sorensen, E.J.3
-
35
-
-
0033980986
-
-
(a) Paquette, L. A.; Barriault, L.; Pissarnitski, D.; Johnston, J. N. J. Am. Chem. Soc. 2000, 122, 619.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 619
-
-
Paquette, L.A.1
Barriault, L.2
Pissarnitski, D.3
Johnston, J.N.4
-
36
-
-
0034696109
-
-
(b) Nicolaou, K. C.; Li, Y.; Weyershausen, B.; Wei, H.-X. Chem. Commun. 2000, 307. For an extensive review of the Stille reaction, see
-
(2000)
Chem. Commun.
, pp. 307
-
-
Nicolaou, K.C.1
Li, Y.2
Weyershausen, B.3
Wei, H.-X.4
-
37
-
-
0000802361
-
-
(c) Farina, V.; Krishnamurthy, V.; Scott, W. J. Org. React. 1994, 50, 1.
-
(1994)
Org. React.
, vol.50
, pp. 1
-
-
Farina, V.1
Krishnamurthy, V.2
Scott, W.J.3
-
38
-
-
0042047948
-
-
note
-
The spectral data of 27 resemble the corresponding signals of the SNF compounds. For instance, the vinylic proton at C14 is markedly shifted upfield (δ 5.00 in SNF4435 C, 4.93 in SNF4435 D, and 4.41 in 27).
-
-
-
|