-
1
-
-
0037067558
-
Ammonia free reduction of aromatic compounds using lithium di-tert-butylbiphenyl (LiDBB)
-
Donohoe, T.J. & House, D. Ammonia free reduction of aromatic compounds using lithium di-tert-butylbiphenyl (LiDBB). J. Org. Chem. 67, 5015-5018 (2002).
-
(2002)
J. Org. Chem
, vol.67
, pp. 5015-5018
-
-
Donohoe, T.J.1
House, D.2
-
2
-
-
0032492974
-
The Birch reduction of 3-substituted pyrroles
-
Donohoe, T.J., Guyo, P.M., Harji, R. R. & Cousins, R.P.C. The Birch reduction of 3-substituted pyrroles. Tetrahedron Lett. 39, 3075-3078 (1998).
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 3075-3078
-
-
Donohoe, T.J.1
Guyo, P.M.2
Harji, R.R.3
Cousins, R.P.C.4
-
3
-
-
0033555698
-
The stereoselective Birch reduction of pyrroles
-
Donohoe, T.J., Guyo, P.M. & Helliwell, M. The stereoselective Birch reduction of pyrroles. Tetrahedron Lett. 40, 435-438 (1999).
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 435-438
-
-
Donohoe, T.J.1
Guyo, P.M.2
Helliwell, M.3
-
4
-
-
0032492983
-
Stereoselectivity in the Birch reduction of 2-furoic acid derivatives
-
Donohoe, T.J., Helliwell, M., Stevenson, C.A. & Ladduwahetty, T. Stereoselectivity in the Birch reduction of 2-furoic acid derivatives. Tetrahedron Lett. 39, 3071-3074 (1998).
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 3071-3074
-
-
Donohoe, T.J.1
Helliwell, M.2
Stevenson, C.A.3
Ladduwahetty, T.4
-
5
-
-
0034696661
-
The synthesis of (+)-nemorensic acid
-
Donohoe, T.J., Guillermin, J.-B., Frampton, C. & Walters, D.S. The synthesis of (+)-nemorensic acid. Chem. Commun. 465-466 (2000).
-
(2000)
Chem. Commun
, vol.465-466
-
-
Donohoe, T.J.1
Guillermin, J.-B.2
Frampton, C.3
Walters, D.S.4
-
6
-
-
0036170452
-
Transformations of 3,4-dissubstituted pyridines under dissolving metal conditions-partial reduction followed by radical cyclisation
-
Donohoe, T.J., Mace, L.H., Helliwell, M. & Ichihara, O. Transformations of 3,4-dissubstituted pyridines under dissolving metal conditions-partial reduction followed by radical cyclisation. Synlett 331-333 (2002).
-
(2002)
Synlett
, vol.331-333
-
-
Donohoe, T.J.1
Mace, L.H.2
Helliwell, M.3
Ichihara, O.4
-
7
-
-
0000440720
-
Partial reduction of electron deficient pyridines
-
Donohoe, T.J., McRiner, A.J. & Sheldrake, P. Partial reduction of electron deficient pyridines. Org. Lett. 2, 3861-3863 (2000).
-
(2000)
Org. Lett
, vol.2
, pp. 3861-3863
-
-
Donohoe, T.J.1
McRiner, A.J.2
Sheldrake, P.3
-
8
-
-
13844299285
-
Partial reduction of pyridinium salts as a versatile route to dihydropyridones
-
Donohoe, T.J., Johnson, D.J., Mace, L.H., Bamford, M.J. & Ichihara, O. Partial reduction of pyridinium salts as a versatile route to dihydropyridones. Org. Lett. 7, 435-437 (2005).
-
(2005)
Org. Lett
, vol.7
, pp. 435-437
-
-
Donohoe, T.J.1
Johnson, D.J.2
Mace, L.H.3
Bamford, M.J.4
Ichihara, O.5
-
9
-
-
0001570826
-
Birch reduction of electron-deficient pyrroles
-
Donohoe, T.J. & Guyo, P.M. Birch reduction of electron-deficient pyrroles. J. Org. Chem. 61, 7664-7665 (1996).
-
(1996)
J. Org. Chem
, vol.61
, pp. 7664-7665
-
-
Donohoe, T.J.1
Guyo, P.M.2
-
10
-
-
0344550536
-
Scope of the reductive aldol reaction: Application to aromatic carbocycles and heterocycles
-
Donohoe, T.J., House, D. & Ace, K.W. Scope of the reductive aldol reaction: Application to aromatic carbocycles and heterocycles. Org. Biomol. Chem. 1, 3749-3757 (2003).
-
(2003)
Org. Biomol. Chem
, vol.1
, pp. 3749-3757
-
-
Donohoe, T.J.1
House, D.2
Ace, K.W.3
-
11
-
-
0037467888
-
Diastereoselective reductive aldol reactions of Boc-protected electron deficient pyrroles
-
Donohoe, T.J. & House, D. Diastereoselective reductive aldol reactions of Boc-protected electron deficient pyrroles. Tetrahedron Lett. 44, 1095-1098 (2003).
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 1095-1098
-
-
Donohoe, T.J.1
House, D.2
-
12
-
-
1842483974
-
Enantiopure oxazolidinones as chiral acids in the asymmetric protonation of N-Boc pyrrole derived enolates
-
Carbery, D.R. & Donohoe, T.J. Enantiopure oxazolidinones as chiral acids in the asymmetric protonation of N-Boc pyrrole derived enolates. Chem. Commun. 722-723 (2004).
-
(2004)
Chem. Commun
, vol.722-723
-
-
Carbery, D.R.1
Donohoe, T.J.2
-
13
-
-
4544248644
-
Enantioselective partial reduction of 2,5-disubstituted pyrroles via a chiral protonation approach
-
Donohoe, T.J. et al. Enantioselective partial reduction of 2,5-disubstituted pyrroles via a chiral protonation approach. Org. Lett. 6, 3055-3058 (2004).
-
(2004)
Org. Lett
, vol.6
, pp. 3055-3058
-
-
Donohoe, T.J.1
-
14
-
-
0037572030
-
Flexibility in the partial reduction of 2,5-disubstituted pyrroles: Application to the synthesis of DMDP
-
Donohoe, T.J., Headley, C.E., Cousins, R.P.C. & Cowley, A. Flexibility in the partial reduction of 2,5-disubstituted pyrroles: Application to the synthesis of DMDP. Org. Lett. 5, 999-1002 (2003).
-
(2003)
Org. Lett
, vol.5
, pp. 999-1002
-
-
Donohoe, T.J.1
Headley, C.E.2
Cousins, R.P.C.3
Cowley, A.4
-
16
-
-
22044438998
-
Utility of the ammonia-free Birch reduction of electron-deficient pyrroles: Total synthesis of the 20S proteasome inhibitor, clasto-lactacystin β-lactone
-
Donohoe, T.J. et al. Utility of the ammonia-free Birch reduction of electron-deficient pyrroles: Total synthesis of the 20S proteasome inhibitor, clasto-lactacystin β-lactone. Chem. Eur. J. 11, 4227-4238 (2005).
-
(2005)
Chem. Eur. J
, vol.11
, pp. 4227-4238
-
-
Donohoe, T.J.1
-
17
-
-
34548260247
-
Formation of N-Boc pyrrole 2-ethyl ester, a key intermediate in the Donohoe synthesis of omuralide
-
DOI: 10.1038/nprot.2007.231
-
Donohoe, T.J. & Thomas, R.E. Formation of N-Boc pyrrole 2-ethyl ester, a key intermediate in the Donohoe synthesis of omuralide. Nat. Protoc. DOI: 10.1038/nprot.2007.231 (2007).
-
(2007)
Nat. Protoc
-
-
Donohoe, T.J.1
Thomas, R.E.2
-
18
-
-
3042839948
-
A concise total synthesis of (±)-1-epiaustraline
-
Donohoe, T.J. & Sintim, H.O. A concise total synthesis of (±)-1-epiaustraline. Org. Lett. 6, 2003-2006 (2004).
-
(2004)
Org. Lett
, vol.6
, pp. 2003-2006
-
-
Donohoe, T.J.1
Sintim, H.O.2
-
20
-
-
4043159247
-
An efficient synthesis of lactacystin β-lactone
-
Donohoe, T.J., Sintim, H.O., Sisangia, L. & Harting, J.D. An efficient synthesis of lactacystin β-lactone. Angew. Chem. Int. Ed. 43 2293-2296 (2004).
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 2293-2296
-
-
Donohoe, T.J.1
Sintim, H.O.2
Sisangia, L.3
Harting, J.D.4
-
21
-
-
0000733116
-
Electron spin resonance spectra of some group IV-B substituted biphenyl anion radicals. Dative π-bonding
-
Curtis, M.D. & Allred, A.L. Electron spin resonance spectra of some group IV-B substituted biphenyl anion radicals. Dative π-bonding. J. Am. Chem. Soc. 87, 2554-2563 (1965).
-
(1965)
J. Am. Chem. Soc
, vol.87
, pp. 2554-2563
-
-
Curtis, M.D.1
Allred, A.L.2
-
22
-
-
34548242125
-
-
Rieke, R.D., Bates, S.E., Hudnall, P.M., Burns, T.P., Poindexter, G.S. Highly reactive magnesium for the preparation of Grignard reagents: 1-norbornanecarboxylic acid. Org. Synth. Coll. 6, 845-851 (1988); 59, 85-91 (1979).
-
Rieke, R.D., Bates, S.E., Hudnall, P.M., Burns, T.P., Poindexter, G.S. Highly reactive magnesium for the preparation of Grignard reagents: 1-norbornanecarboxylic acid. Org. Synth. Coll. Vol. 6, 845-851 (1988); 59, 85-91 (1979).
-
-
-
-
23
-
-
5244370033
-
Safe and convenient procedure for solvent purification
-
Pangborn, A.B., Giardello, M.A., Grubbs, R.H., Rosen, R.K. & Timmers, F.J. Safe and convenient procedure for solvent purification. Organometallics 15, 1518-1520 (1996).
-
(1996)
Organometallics
, vol.15
, pp. 1518-1520
-
-
Pangborn, A.B.1
Giardello, M.A.2
Grubbs, R.H.3
Rosen, R.K.4
Timmers, F.J.5
|