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1
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0035471135
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β-Peptides from structure to function
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Cheng, R.P.; Gellman, S.H.; DeGrado, W.F. β-Peptides: from structure to function. Chem. Rev. 2001, 101, 3219.
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(2001)
Chem. Rev.
, vol.101
, pp. 3219
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Cheng, R.P.1
Gellman, S.H.2
DeGrado, W.F.3
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2
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0028130028
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Recent stereoselective synthetic approaches to β-amino acids
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For reviews, see: Cole, D.C. Recent stereoselective synthetic approaches to β-amino acids. Tetrahedron 1994, 50, 9517.
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(1994)
Tetrahedron.
, vol.50
, pp. 9517
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Cole, D.C.1
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3
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0345466641
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3-Homoproline: What are the secondary structures of β-peptides lacking H-bonds?
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3-Homoproline: what are the secondary sturctures of β-peptides lacking H-bonds? Helv. Chim. Acta 1999, 82, 1539.
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(1999)
Helv. Chim. Acta
, vol.82
, pp. 1539
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Abele, S.1
Vögtli, K.2
Seebach, D.3
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4
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0000434355
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Synthesis of the enantiomeric 2-pyrrolidineacetic acids
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(a) Cassal, J.M.; Fuerst, A.; Meier, W.; Synthesis of the enantiomeric 2-pyrrolidineacetic acids. Helv. Chim. Acta 1976, 59, 1917;
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(1976)
Helv. Chim. Acta
, vol.59
, pp. 1917
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Cassal, J.M.1
Fuerst, A.2
Meier, W.3
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5
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0016694535
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Synthesis of α-L-homoproline and derivatives. Preparation of 7-α-L-homoprolinebradykinin
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(b) Balaspiri, L.; Penke, B.; Papp, G.; Dombi, G.; Kovacs, K. Synthesis of α-L-homoproline and derivatives. Preparation of 7-α -L-homoprolinebradykinin. Helv. Chim. Acta 1975, 58, 969;
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(1975)
Helv. Chim. Acta
, vol.58
, pp. 969
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Balaspiri, L.1
Penke, B.2
Papp, G.3
Dombi, G.4
Kovacs, K.5
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6
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0017763809
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Contribution to the asymmetric synthesis of bicyclic compounds catalyzed by optically active amino acids. Synthesis of (S)-2-pyrrolidinepropionic acid and (R)-4-amino-5-phenylvaleric acid
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(c) Buchschacher, P.; Cassal, J.M.; Fuerst, A.; Meier, W.; Contribution to the asymmetric synthesis of bicyclic compounds catalyzed by optically active amino acids. Synthesis of (S)-2-pyrrolidinepropionic acid and (R)-4-amino-5-phenylvaleric acid. Helv. Chim. Acta 1977, 60, 2747.
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(1977)
Helv. Chim. Acta
, vol.60
, pp. 2747
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Buchschacher, P.1
Cassal, J.M.2
Fuerst, A.3
Meier, W.4
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7
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0345492501
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note
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4: C, 71.37; H, 6.56; N, 3.96. Found: C, 71.19; H, 6.49; N, 4.05. For both two compounds, the existence of rotator is observed in their NMR spectra.
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8
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0345060945
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note
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2: C, 71.21; H, 7.81; N, 6.39. Found: C, 70.87; H, 7.81; N, 6.45.
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9
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0344630364
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note
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2; 244.1212. Found: 244.1212.
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10
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0344198681
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(Phenylacetyl)urea. U. S. S. R. 432, 136, 1974
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(a) Semikolennykh, L.M.; Katsnel'son, M.G.; Del'nik, V.B. (Phenylacetyl)urea. U. S. S. R. 432, 136, 1974;
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Semikolennykh, L.M.1
Katsnel'son, M.G.2
Del'nik, V.B.3
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11
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0344630365
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5- (Or 1, 5-Di-) Substituted uracil derivatives. Ger. (East) DD 1985, 222, 591
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(b) Seres, J.; Daroczi, K.; Seres, P.; Koszegi, B. 5- (Or 1, 5-Di-) Substituted uracil derivatives. Ger. (East) DD 1985, 222, 591.
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Seres, J.1
Daroczi, K.2
Seres, P.3
Koszegi, B.4
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12
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33748654012
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Azabicyclo[3. 2. 0] heptan-7-ones (carbapenams) from Pyrrole
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Gilchrist, T.L.; Lemos, A.; Ottaway, C.J. Azabicyclo[3. 2. 0] heptan-7-ones (carbapenams) from Pyrrole. J. Chem. Soc. Perkin Trans. 1 1997, 19, 3005.
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(1997)
J. Chem. Soc. Perkin Trans. 1
, vol.19
, pp. 3005
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Gilchrist, T.L.1
Lemos, A.2
Ottaway, C.J.3
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13
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0027930134
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Free radical rearrangements in uracil derivatives
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Fenick, D.J.; Falvey, D.E. Free radical rearrangements in uracil derivatives. J. Org. Chem. 1994, 59, 4791.
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(1994)
J. Org. Chem.
, vol.59
, pp. 4791
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Fenick, D.J.1
Falvey, D.E.2
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14
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0345060949
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note
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b supported the (4S, 4aS) configuration of 4.
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