-
13
-
-
0010735543
-
-
R. Kober, K. Papadopoulos, W. Miltz, D. Enders, W. Steglich, H. Reuter, and H. Puff Tetrahedron 42 1985 1963
-
(1985)
Tetrahedron
, vol.42
, pp. 1963
-
-
Kober, R.1
Papadopoulos, K.2
Miltz, W.3
Enders, D.4
Steglich, W.5
Reuter, H.6
Puff, H.7
-
18
-
-
33748468588
-
-
D.A. Evans, F. Urpi, T.C. Somers, J.S. Clark, and M.T. Bilodeau J. Am. Chem. Soc. 112 1990 8215
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 8215
-
-
Evans, D.A.1
Urpi, F.2
Somers, T.C.3
Clark, J.S.4
Bilodeau, M.T.5
-
19
-
-
0037167030
-
-
C. Palomo, M. Oiarbide, A. Landa, M.C. Gonzales-Rego, J.M. Garcia, A. Gonzales, J.M. Odriozola, M. Martin-Pastor, and A. Linden J. Am. Chem. Soc. 124 2002 8637 and references therein
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 8637
-
-
Palomo, C.1
Oiarbide, M.2
Landa, A.3
Gonzales-Rego, M.C.4
Garcia, J.M.5
Gonzales, A.6
Odriozola, J.M.7
Martin-Pastor, M.8
Linden, A.9
-
25
-
-
0000603617
-
-
D. Ferraris, B. Young, C. Cox, W.J. Drury III, T. Dudding, and T. Lectka J. Org. Chem. 63 1998 6090
-
(1998)
J. Org. Chem.
, vol.63
, pp. 6090
-
-
Ferraris, D.1
Young, B.2
Cox, C.3
Drury III, W.J.4
Dudding, T.5
Lectka, T.6
-
26
-
-
0037045227
-
-
D. Ferraris, B. Young, C. Cox, T. Dudding, W.J. Drury III, L. Ryzhkov, T. Taggi, and T. Lectka J. Am. Chem. Soc. 124 2002 67
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 67
-
-
Ferraris, D.1
Young, B.2
Cox, C.3
Dudding, T.4
Drury III, W.J.5
Ryzhkov, L.6
Taggi, T.7
Lectka, T.8
-
29
-
-
0037462104
-
-
S. Matsunaga, N. Kumagai, N. Harada, S. Harada, and M. Shibasaki J. Am. Chem. Soc. 125 2003 4712
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 4712
-
-
Matsunaga, S.1
Kumagai, N.2
Harada, N.3
Harada, S.4
Shibasaki, M.5
-
32
-
-
0037495950
-
-
M. Marigo, A. Kjaersgaard, K. Juhl, N. Gathergood, and K.A. Jørgensen Chem. Eur. J. 9 2003 2359
-
(2003)
Chem. Eur. J.
, vol.9
, pp. 2359
-
-
Marigo, M.1
Kjaersgaard, A.2
Juhl, K.3
Gathergood, N.4
Jørgensen, K.A.5
-
40
-
-
0035825097
-
-
W. Notz, K. Sakthivel, T. Bui, G. Zhong, and C.F. Barbas III Tetrahedron Lett. 42 2001 199
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 199
-
-
Notz, W.1
Sakthivel, K.2
Bui, T.3
Zhong, G.4
Barbas III, C.F.5
-
41
-
-
0037028924
-
-
A. Córdova, W. Notz, G. Zhong, J.M. Betancort, and C.F. Barbas III J. Am. Chem. Soc. 124 2002 1842
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1842
-
-
Córdova, A.1
Notz, W.2
Zhong, G.3
Betancort, J.M.4
Barbas III, C.F.5
-
43
-
-
0344927944
-
-
T. Itoh, M. Yokoya, K. Miyauchi, K. Nagata, and A. Ohsawa Org. Lett. 5 2003 4301
-
(2003)
Org. Lett.
, vol.5
, pp. 4301
-
-
Itoh, T.1
Yokoya, M.2
Miyauchi, K.3
Nagata, K.4
Ohsawa, A.5
-
45
-
-
0037028990
-
-
Aldehydes as donors see: A. Córdova, S.-I. Watanabe, F. Tanaka, W. Notz, and C.F. Barbas III J. Am. Chem. Soc. 124 2002 1866
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1866
-
-
Córdova, A.1
Watanabe, S.-I.2
Tanaka, F.3
Notz, W.4
Barbas III, C.F.5
-
50
-
-
0042969372
-
-
Y. Hayashi, W. Tsuboi, I. Ashimine, T. Urushima, M. Shoji, and K. Sakai Angew. Chem. Int. Ed. 42 2003 3677
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 3677
-
-
Hayashi, Y.1
Tsuboi, W.2
Ashimine, I.3
Urushima, T.4
Shoji, M.5
Sakai, K.6
-
60
-
-
3242806955
-
-
For proline-catalyzed synthesis of protected tetroses via aldol reactions, see: A.B. Northrup, I.K. Mangion, F. Hettche, and D.W.C. MacMillan Angew. Chem. Int. Ed. 43 2004 2152
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 2152
-
-
Northrup, A.B.1
Mangion, I.K.2
Hettche, F.3
MacMillan, D.W.C.4
-
61
-
-
14844283105
-
-
For amino acid catalyzed asymmetric synthesis of tetroses and hexoses, see: J. Casas, M. Engqvist, I. Ibrahem, B. Kaynak, and A. Córdova Angew. Chem. Int. Ed. 44 2005 1343
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 1343
-
-
Casas, J.1
Engqvist, M.2
Ibrahem, I.3
Kaynak, B.4
Córdova, A.5
-
62
-
-
85030814288
-
-
Córdova, A.; Ibrahem, I.; Casas, J.; Sundén, H.; Engqvist, M.; Reyes, E. The tetroses derived by proline catalysis can also be converted to hexoses by their utilization as acceptors in Lewis acid-catalyzed indirect Mukaiyama aldol reactions, see:
-
The Tetroses Derived by Proline Catalysis Can Also Be Converted to Hexoses by Their Utilization As Acceptors in Lewis Acid-catalyzed Indirect Mukaiyama Aldol Reactions
-
-
Córdova, A.1
Ibrahem, I.2
Casas, J.3
Sundén, H.4
Engqvist, M.5
Reyes, E.6
-
69
-
-
3242814515
-
-
A. Córdova, H. Sundén, M. Engqvist, I. Ibrahem, and J. Casas J. Am. Chem. Soc. 126 2004 8914
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8914
-
-
Córdova, A.1
Sundén, H.2
Engqvist, M.3
Ibrahem, I.4
Casas, J.5
-
70
-
-
11144326714
-
-
H. Sundén, M. Engqvist, J. Casas, I. Ibrahem, and A. Córdova Angew. Chem. Int. Ed. 43 2004 6532
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 6532
-
-
Sundén, H.1
Engqvist, M.2
Casas, J.3
Ibrahem, I.4
Córdova, A.5
-
72
-
-
4243126802
-
-
A. Córdova, H. Sundén, A. Bøgevig, M. Johansson, and F. Himo Chem. Eur. J. 10 2004 3673
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 3673
-
-
Córdova, A.1
Sundén, H.2
Bøgevig, A.3
Johansson, M.4
Himo, F.5
-
73
-
-
85030807947
-
-
note
-
+: calcd 430.1994)
-
-
-
-
74
-
-
85030816933
-
-
note
-
The compounds are sensitive and they epimerize and racemize upon silica-gel column chromatography. The β-amino-α-oxyaldehyde products should be stored at -35°C
-
-
-
-
75
-
-
85030812699
-
-
note
-
11a,11b
-
-
-
-
76
-
-
21844482982
-
-
Protected amino alcohol 1a was converted to the known peracetylated (2R,3S)-2-aminothreitol with [ α ] D 24 + 40 (c = 0.1, MeOH). The reported optical rotation for peracetylated (2R,3S)-aminothreitol is [ α ] D 25 + 40.3 (c = 1.12, MeOH) P.A. Wade, and S.G. D'Ambrosio J. Carbohydr. Chem. 14 1995 1329
-
(1995)
J. Carbohydr. Chem.
, vol.14
, pp. 1329
-
-
Wade, P.A.1
D'Ambrosio, S.G.2
|