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4
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56749090805
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For review, see:
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For review, see:. Veitch G.E., Boyer A., and Ley S.V. Angew. Chem., Int. Ed. 47 (2008) 9402
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Veitch, G.E.1
Boyer, A.2
Ley, S.V.3
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5
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35048889990
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for total synthesis, see:
-
for total synthesis, see:. Veitch G.E., Beckmann E., Burke B.J., Boyer A., Maslen S.L., and Ley S.V. Angew. Chem., Int. Ed. 46 (2007) 7629
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Veitch, G.E.1
Beckmann, E.2
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Boyer, A.4
Maslen, S.L.5
Ley, S.V.6
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6
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35048900932
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Veitch G.E., Beckmann E., Burke B.J., Boyer A., Ayats C., and Ley S.V. Angew. Chem., Int. Ed. 46 (2007) 7633
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Veitch, G.E.1
Beckmann, E.2
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Boyer, A.4
Ayats, C.5
Ley, S.V.6
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7
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56749155796
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Ley S.V., Somovilla A.A., Anderson J.C., Ayats C., Bänteli R., Beckmann E., Boyer A., Brasca M.G., Brice A., Broughton H.B., Burke B.J., Cleator E., Craig D., Denholm A.A., Denton R.M., Reville T.D., Gobbi L.B., Göbel M., Gray B.L., Grossmann R.B., Gutteridge C.E., Hahn N., Harding S.L., Jennens D.C., Jennens L., Lovell P.J., Lovell H.J., Puente M.L., Kolb H.C., Koot W.J., Maslen S.L., McCusker C.F., Mattes A., Pape A.R., Pinto A., Santafianos D., Scott J.S., Smith S.C., Somers A.Q., Spilling C.D., Stelzer F., Toogood P.L., Turner R.M., Veitch G.E., Wood A., and Zumbrunn C. Chem. Eur. J. 14 (2008) 10683
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Ley, S.V.1
Somovilla, A.A.2
Anderson, J.C.3
Ayats, C.4
Bänteli, R.5
Beckmann, E.6
Boyer, A.7
Brasca, M.G.8
Brice, A.9
Broughton, H.B.10
Burke, B.J.11
Cleator, E.12
Craig, D.13
Denholm, A.A.14
Denton, R.M.15
Reville, T.D.16
Gobbi, L.B.17
Göbel, M.18
Gray, B.L.19
Grossmann, R.B.20
Gutteridge, C.E.21
Hahn, N.22
Harding, S.L.23
Jennens, D.C.24
Jennens, L.25
Lovell, P.J.26
Lovell, H.J.27
Puente, M.L.28
Kolb, H.C.29
Koot, W.J.30
Maslen, S.L.31
McCusker, C.F.32
Mattes, A.33
Pape, A.R.34
Pinto, A.35
Santafianos, D.36
Scott, J.S.37
Smith, S.C.38
Somers, A.Q.39
Spilling, C.D.40
Stelzer, F.41
Toogood, P.L.42
Turner, R.M.43
Veitch, G.E.44
Wood, A.45
Zumbrunn, C.46
more..
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8
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0013217518
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for recent synthetic studies, see:
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for recent synthetic studies, see:. Fukuzaki T., Kobayashi S., Hibi T., Ikuma Y., Ishihara J., Kanoh N., and Murai A. Org. Lett. 4 (2002) 2877
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Murai, A.7
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9
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20444419068
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Nicolaou K.C., Sasmal P.K., Koftis T.V., Converso E.L., Kaiser F., Roecker A.J., Dellios C.C., Sun X.-W., and Petrovic G. Angew. Chem., Int. Ed. 44 (2005) 3443
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Nicolaou, K.C.1
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Koftis, T.V.3
Converso, E.L.4
Kaiser, F.5
Roecker, A.J.6
Dellios, C.C.7
Sun, X.-W.8
Petrovic, G.9
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20444362418
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Nicolaou K.C., Sasmal P.K., Roecker A.J., Sun X.-W., Mandal S., and Converso A. Angew. Chem., Int. Ed. 44 (2005) 3447
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Nicolaou, K.C.1
Sasmal, P.K.2
Roecker, A.J.3
Sun, X.-W.4
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Converso, A.6
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34247873121
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Watanabe H., Mori N., Itoh D., Kitahara T., and Mori K. Angew. Chem., Int. Ed. 46 (2007) 1512
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Watanabe, H.1
Mori, N.2
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Kitahara, T.4
Mori, K.5
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12
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0001215915
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Trost B.M. (Ed), Blackwell Scientific Publications, Oxford
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Hoffmann R.W. In: Trost B.M. (Ed). Stereocontrolled Organic Synthesis (1994), Blackwell Scientific Publications, Oxford 259-274
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Hoffmann, R.W.1
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14
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0000094579
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Allylboron Reagents
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Stereoselective Synthesis. Ahlbecht H., Helmchean G., Arend M., and Herrmann R. (Eds), Georg Thieme, Stuttgart
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Roush W.R. Allylboron Reagents. In: Ahlbecht H., Helmchean G., Arend M., and Herrmann R. (Eds). Stereoselective Synthesis. Methods in Organic Chemistry E21b (1995), Georg Thieme, Stuttgart 1410-1485
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Roush, W.R.1
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18
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1542763298
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For a review on ring-closing metathesis, see:
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For a review on ring-closing metathesis, see:. Grubbs R.H., Miller S.J., and Fu G.C. Acc. Chem. Res. 28 (1995) 446
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Grubbs, R.H.1
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0033515797
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Low reactivity of enol triflates in epoxidation is reported:
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Low reactivity of enol triflates in epoxidation is reported:. Evarts J.B., and Fuchs P.L. Tetrahedron Lett. 40 (1999) 2703
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Evarts, J.B.1
Fuchs, P.L.2
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22
-
-
77950593620
-
-
note
-
Epimer 28a in which the isopropoxy group is oriented over the B ring exhibited poor reactivity probably because of the steric hindrance around the enol triflate moiety.{A figure is presented}
-
-
-
-
23
-
-
77950593965
-
-
note
-
The stereochemistry of allylborane 30 was determined by the NOE measurements.
-
-
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24
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3242761310
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Miyashita M., Sasaki M., Hattori I., Sakai M., and Tanino K. Science 305 (2004) 495
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Sasaki, M.2
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Tanino, K.5
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25
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67649654327
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Alkenyl lithium 32 was prepared by treating (E)-1-methoxy-3-(tributylstannyl)-2-butene with butyllithium. For the synthesis of (E)-3-(tributylstannyl)-2-buten-1-ol, see:
-
Alkenyl lithium 32 was prepared by treating (E)-1-methoxy-3-(tributylstannyl)-2-butene with butyllithium. For the synthesis of (E)-3-(tributylstannyl)-2-buten-1-ol, see:. Yoshimura F., Sasaki M., Hattori I., Komatsu K., Sakai M., Tanino K., and Miyashita M. Chem. Eur. J. 15 (2009) 6626
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Yoshimura, F.1
Sasaki, M.2
Hattori, I.3
Komatsu, K.4
Sakai, M.5
Tanino, K.6
Miyashita, M.7
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