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1
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0025074114
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For recent reviews see for instance: (a)
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For recent reviews see for instance: (a) Stammer, C. H.; Tetrahedron 1990, 46, 2231-2254.
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(1990)
Tetrahedron
, vol.46
, pp. 2231-2254
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Stammer, C.H.1
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3
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37049112292
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(a)
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(a) Baldwin, J. E.; Adlington, R. M.; Lajoie, G. A.; Rawlings, B. J. J. Chem. Soc., Chem. Commun. 1985, 1496-1498.
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J. Chem. Soc., Chem. Commun.
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Baldwin, J.E.1
Adlington, R.M.2
Lajoie, G.A.3
Rawlings, B.J.4
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4
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0001060253
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(b)
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(b) Baldwin, J. E.; Adlington, R. M.; Rawlings, B. J. Tetrahedron Lett. 1985, 26, 481-484.
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(1985)
Tetrahedron Lett.
, vol.26
, pp. 481-484
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Baldwin, J.E.1
Adlington, R.M.2
Rawlings, B.J.3
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6
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0001566441
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(d)
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(d) Aitken, D. J.; Royer, J.; Husson, H.-P. J. Org. Chem. 1990, 55, 2814-2820.
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J. Org. Chem.
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Aitken, D.J.1
Royer, J.2
Husson, H.-P.3
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7
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0000561351
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Hill, R. K.; Prakash, S. R.; Wiesendanger, R.; Angst, W.; Martinoni, B.; Arigoni, D.; Liu, H. W.; Walsh, C. T. J. Am. Chem. Soc. 1984, 106, 795-796.
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Hill, R.K.1
Prakash, S.R.2
Wiesendanger, R.3
Angst, W.4
Martinoni, B.5
Arigoni, D.6
Liu, H.W.7
Walsh, C.T.8
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8
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0029908901
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2c ACCs also have important applications in the design and synthesis of peptidomimetics. See, for instance
-
2c ACCs also have important applications in the design and synthesis of peptidomimetics. See, for instance: Burgess, K.; Ke, C.-Y. J. Org. Chem. 1996, 61, 8627-8631.
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(1996)
J. Org. Chem.
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Burgess, K.1
Ke, C.-Y.2
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9
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0029115974
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(a)
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(a) Cativiela, C.; Diaz-de-Villegas, M. D.; Jiménez, A. I. Tetrahedron: Asymmetry 1995, 6, 2067-2072.
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(1995)
Tetrahedron: Asymmetry
, vol.6
, pp. 2067-2072
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Cativiela, C.1
Diaz-De-Villegas, M.D.2
Jiménez, A.I.3
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10
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0038459459
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(b)
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(b) Jiménez, J. J.; Rifé, J.; Ortuño, R. Tetrahedron: Asymmetry 1996, 7, 537-558.
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(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 537-558
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Jiménez, J.J.1
Rifé, J.2
Ortuño, R.3
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13
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0343183019
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(e)
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(e) Hercouet, A.; Bessieres, B.; Le Corre. M. Tetrahedron: Asymmetry, 1996, 7, 283-284.
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(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 283-284
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Hercouet, A.1
Bessieres, B.2
Le Corre., M.3
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14
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0023872535
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DDAA derivatives represent an important type of compound as key intermediates in amino acid and peptide synthesis and as constituents of naturally occurring peptides with potent antimicrobial and phytotoxic activities. For reviews see: (a)
-
DDAA derivatives represent an important type of compound as key intermediates in amino acid and peptide synthesis and as constituents of naturally occurring peptides with potent antimicrobial and phytotoxic activities. For reviews see: (a) Schmidt, U.; Lieberknecht, A.; Wild, J. Synthesis 1988, 159-172.
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(1988)
Synthesis
, pp. 159-172
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Schmidt, U.1
Lieberknecht, A.2
Wild, J.3
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16
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0025793573
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(a)
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(a) Alami, A.; Calmes, M.; Daunis, J.; Escale, F.; Jacquier, R.; Roumestant, M.-L.; Viallefont, P. Tetrahedron: Asymmetry 1991, 2, 175-178.
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(1991)
Tetrahedron: Asymmetry
, vol.2
, pp. 175-178
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-
Alami, A.1
Calmes, M.2
Daunis, J.3
Escale, F.4
Jacquier, R.5
Roumestant, M.-L.6
Viallefont, P.7
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17
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0026590608
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(b)
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(b) Cativiela, C.; Diaz-de-Villegas, M. D.; Gálvez, J. A. Tetrahedron: Asymmetry 1992, 3, 567-572.
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(1992)
Tetrahedron: Asymmetry
, vol.3
, pp. 567-572
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Cativiela, C.1
Diaz-De-Villegas, M.D.2
Gálvez, J.A.3
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18
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0030063822
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(c)
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(c) Calmes, M.; Daunis, J.; Escale, F. Tetrahedron: Asymmetry 1996, 7, 395-396.
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(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 395-396
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Calmes, M.1
Daunis, J.2
Escale, F.3
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23
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0004417286
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(h)
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(h) Alcaraz, C.; Fernández, M. D.; de Frutos, M. P.; Marco, J. L.; Bernabé, M.; Foces-Foces, C.; Cano, F. H. Tetrahedron 1994, 50, 12433-12456.
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(1994)
Tetrahedron
, vol.50
, pp. 12433-12456
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Alcaraz, C.1
Fernández, M.D.2
De Frutos, M.P.3
Marco, J.L.4
Bernabé, M.5
Foces-Foces, C.6
Cano, F.H.7
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24
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0027301506
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Chinchilla, R.; Nájera, C.; García-Granda, S.; Menéndez-Velázquez, A. Tetrahedron Lett. 1993, 34, 5799-5802.
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(1993)
Tetrahedron Lett.
, vol.34
, pp. 5799-5802
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Chinchilla, R.1
Nájera, C.2
García-Granda, S.3
Menéndez-Velázquez, A.4
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25
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0030905372
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Chinchilla, R.; Falvello, L. R.; Galindo, N.; Nájera, C. Angew. Chem. Int. Ed. Engl. 1997, 36, 995-997.
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(1997)
Angew. Chem. Int. Ed. Engl.
, vol.36
, pp. 995-997
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Chinchilla, R.1
Falvello, L.R.2
Galindo, N.3
Nájera, C.4
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26
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0010711247
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546 +20 (c, 2.2; 95% EtOH) The preparation of 12 following this literature procedure afforded very low yields
-
546 +20 (c, 2.2; 95% EtOH): Maigrot, N.; Mazaleyrat, J.-P.; Welvart, Z. J. Org. Chem. 1985, 50, 3916-3918. The preparation of 12 following this literature procedure afforded very low yields.
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(1985)
J. Org. Chem.
, vol.50
, pp. 3916-3918
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Maigrot, N.1
Mazaleyrat, J.-P.2
Welvart, Z.3
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27
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0025036824
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-
This acid is commercially available (Aldrich) or can be prepared by diazotization of L-valine
-
This acid is commercially available (Aldrich) or can be prepared by diazotization of L-valine: Li, W.-R.; Ewing, W. R.; Harris, B. D.; Jouillé, M. M. J. Am. Chem. Soc. 1990, 112, 7659-7672.
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J. Am. Chem. Soc.
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, pp. 7659-7672
-
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Li, W.-R.1
Ewing, W.R.2
Harris, B.D.3
Jouillé, M.M.4
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28
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0006386142
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Ward, D. E.; Vázquez, A.; Pedras, M. S. C. J. Org. Chem. 1996, 61, 8008-8009.
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Ward, D.E.1
Vázquez, A.2
Pedras, M.S.C.3
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29
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0344046144
-
-
note
-
-1. Full structural details have been deposited with the Cambridge Crystallographic Data Centre.
-
-
-
-
30
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-
33947485009
-
-
For a recent review on asymmetric ylide reactions see
-
Corey, E. J.; Chaykovsky, M. J. Am. Chem. Soc. 1965, 87, 1353-1364. For a recent review on asymmetric ylide reactions see: Li, A.-H.; Dai, L.-X.; Aggarzwal, V. K. Chem. Rev. 1997, 97, 2341-2372.
-
(1965)
J. Am. Chem. Soc.
, vol.87
, pp. 1353-1364
-
-
Corey, E.J.1
Chaykovsky, M.2
-
31
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0001485086
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Corey, E. J.; Chaykovsky, M. J. Am. Chem. Soc. 1965, 87, 1353-1364. For a recent review on asymmetric ylide reactions see: Li, A.-H.; Dai, L.-X.; Aggarzwal, V. K. Chem. Rev. 1997, 97, 2341-2372.
-
(1997)
Chem. Rev.
, vol.97
, pp. 2341-2372
-
-
Li, A.-H.1
Dai, L.-X.2
Aggarzwal, V.K.3
-
32
-
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0009781138
-
-
2O)
-
2O): Baldwin, J. E.; Adlington, R. M.; Rawlings, B. J.; Jones, R. H. Tetrahedron Lett. 1985, 26, 485-488.
-
(1985)
Tetrahedron Lett.
, vol.26
, pp. 485-488
-
-
Baldwin, J.E.1
Adlington, R.M.2
Rawlings, B.J.3
Jones, R.H.4
-
33
-
-
0344046142
-
-
note
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2O).
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