-
1
-
-
0027971096
-
-
P. A. Horton, F. E. Koehn, R. E. Longley, O. J. McConnell, J. Am. Chem. Soc. 1994, 116, 6015-6016.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 6015-6016
-
-
Horton, P.A.1
Koehn, F.E.2
Longley, R.E.3
McConnell, O.J.4
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2
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0031562078
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M. Nowakowski, H. M. R. Hoffmann, Tetrahedron Lett. 1997, 38, 1001. See also: M. K. Gurjar, A. Chakrabarti, B. V. Rao, P. Kumar, Tetrahedron Lett. 1997, 38, 6885; M. K. Gurjar, P. Kumar, B. V. Rao, Tetrahedron Lett. 1996, 37, 8617.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 1001
-
-
Nowakowski, M.1
Hoffmann, H.M.R.2
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3
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0030818229
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M. Nowakowski, H. M. R. Hoffmann, Tetrahedron Lett. 1997, 38, 1001. See also: M. K. Gurjar, A. Chakrabarti, B. V. Rao, P. Kumar, Tetrahedron Lett. 1997, 38, 6885; M. K. Gurjar, P. Kumar, B. V. Rao, Tetrahedron Lett. 1996, 37, 8617.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 6885
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-
Gurjar, M.K.1
Chakrabarti, A.2
Rao, B.V.3
Kumar, P.4
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4
-
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16144365082
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M. Nowakowski, H. M. R. Hoffmann, Tetrahedron Lett. 1997, 38, 1001. See also: M. K. Gurjar, A. Chakrabarti, B. V. Rao, P. Kumar, Tetrahedron Lett. 1997, 38, 6885; M. K. Gurjar, P. Kumar, B. V. Rao, Tetrahedron Lett. 1996, 37, 8617.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 8617
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Gurjar, M.K.1
Kumar, P.2
Rao, B.V.3
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5
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0033597387
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[3a] Spongistatin C29-C37 segment: R. Dunkel, J. Treu, H. M. R. Hoffmann, Tetrahedron: Asymmetry 1999, 10, 1539.
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(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 1539
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Dunkel, R.1
Treu, J.2
Hoffmann, H.M.R.3
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6
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0033118794
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[3b] Discodermolide C1-C7 segment and Phorboxazole C20-C26 segment: A. Misske, H. M. R. Hoffmann, Tetrahedron 1999, 55, 4315.
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(1999)
Tetrahedron
, vol.55
, pp. 4315
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Misske, A.1
Hoffmann, H.M.R.2
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9
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0030826899
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[3e] Mevinic Acids tetrahydropyran unit: R. Dunkel, M. Mentzel, H. M. R. Hoffmann, Tetrahedron 1997, 53, 14929.
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(1997)
Tetrahedron
, vol.53
, pp. 14929
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Dunkel, R.1
Mentzel, M.2
Hoffmann, H.M.R.3
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11
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85088333097
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note
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[2]
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13
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85088331971
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note
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[3a]
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14
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85088332068
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note
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[3b]
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17
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0002232935
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A "racemic switch" has been defined as "the redevelopment in single-enantiomer form of a drug that was first approved as a racemate"; see: S. C. Stinson, Chem. Eng. News 1998, September 21, 83-104. In our case the early racemic switch provides two key single-isomer precursors of structurally different bioactive natural products.
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(1998)
Chem. Eng. News
, vol.SEPTEMBER 21
, pp. 83-104
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Stinson, S.C.1
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18
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25944457640
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unpublished work
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[8a] P. Schäfer, unpublished work.
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Schäfer, P.1
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19
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25944460525
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PhD thesis, in preparation
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[8b] The ozonolysis was performed following a lead by: P. Schäfer, PhD thesis, in preparation.
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Schäfer, P.1
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20
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0028843898
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[9a] K. Gerth, D. Schummer, G. Höfle, H. Irschik, H. Reichenbach, J. Antibiotics 1995, 48, 973.
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(1995)
J. Antibiotics
, vol.48
, pp. 973
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Gerth, K.1
Schummer, D.2
Höfle, G.3
Irschik, H.4
Reichenbach, H.5
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21
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84988074680
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[9b] D. Schummer, K. Gerth, H. Reichenbach, G. Höfle, Liebigs Ann. 1995, 685.
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(1995)
Liebigs Ann.
, vol.685
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Schummer, D.1
Gerth, K.2
Reichenbach, H.3
Höfle, G.4
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23
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0026325277
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2Et was prepared according to the procedure recorded in: C. Patois, P. Savignac, Synth. Commun. 1991, 21, 2391.
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(1991)
Synth. Commun.
, vol.21
, pp. 2391
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Patois, C.1
Savignac, P.2
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24
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0344786972
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note
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The yield is 12% with respect to the early racemic switch rac-1.
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