-
2
-
-
0001399971
-
Total synthesis of bioactive marine macrolides
-
Norcross, R. D.; Paterson, I. Total synthesis of bioactive marine macrolides. Chem. Rev. 1995, 95, 2041-2114.
-
(1995)
Chem. Rev.
, vol.95
, pp. 2041-2114
-
-
Norcross, R.D.1
Paterson, I.2
-
3
-
-
15844366864
-
Synthetic routes to tetrahydrofuran, tetrahydropyran, and spiroketal units of polyether antibiotics and a survey of spiroketals of other natural products
-
Biovin, T. L. B. Synthetic routes to tetrahydrofuran, tetrahydropyran, and spiroketal units of polyether antibiotics and a survey of spiroketals of other natural products. Tetrahedron 1987, 43, 3309-3362.
-
(1987)
Tetrahedron
, vol.43
, pp. 3309-3362
-
-
Biovin, T.L.B.1
-
4
-
-
33646403425
-
Strategies for the formation of tetrahydropyran rings in the synthesis of natural products
-
Clarke, P. A.; Santos, S. Strategies for the formation of tetrahydropyran rings in the synthesis of natural products. Eur. J. Org. Chem. 2006, 71, 2045-2053.
-
(2006)
Eur. J. Org. Chem.
, vol.71
, pp. 2045-2053
-
-
Clarke, P.A.1
Santos, S.2
-
6
-
-
0037015436
-
Prins cyclizations: Labeling studies and application to natural product synthesis
-
Crosby, S. R.; Harding, J. R.; King, C. D.; Parker, G. D.; Willis, C. L. Prins cyclizations: Labeling studies and application to natural product synthesis. Org. Lett. 2002, 4, 3407-3410.
-
(2002)
Org. Lett.
, vol.4
, pp. 3407-3410
-
-
Crosby, S.R.1
Harding, J.R.2
King, C.D.3
Parker, G.D.4
Willis, C.L.5
-
7
-
-
0036354669
-
Tandem ene-reaction/Intramolecular Sakurai cyclisation (IMSC): A novel access to polysubstituted tetrahydropyrans and g-butyrolactones using a unique allylation strategy
-
Marko, I. E.; Dumeunier, R.; Leclerq, C; Leroy, B.; Plancher, J. M.; Mekhalfia, A.; Bayston, D. J. Tandem ene-reaction/Intramolecular Sakurai cyclisation (IMSC): A novel access to polysubstituted tetrahydropyrans and g-butyrolactones using a unique allylation strategy. Synthesis 2002, 958-972.
-
(2002)
Synthesis
, pp. 958-972
-
-
Marko, I.E.1
Dumeunier, R.2
Leclerq, C.3
Leroy, B.4
Plancher, J.M.5
Mekhalfia, A.6
Bayston, D.J.7
-
8
-
-
12044250168
-
Polymerized liposomes containing C-glycosides of sialic acid: Potent inhibitors of influenza virus in vitro infectivity
-
Spevak, W.; Nagy, J. O.; Charych, D. H.; Schaefer, M. E.; Gilbert, J. H.; Bednarski, M. D. Polymerized liposomes containing C-glycosides of sialic acid: Potent inhibitors of influenza virus in vitro infectivity. J. Am. Chem. Soc. 1993, 115, 1146-1147.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 1146-1147
-
-
Spevak, W.1
Nagy, J.O.2
Charych, D.H.3
Schaefer, M.E.4
Gilbert, J.H.5
Bednarski, M.D.6
-
10
-
-
0009147056
-
Design and synthesis of a new class of nonmacrocyclic alkali metal host compounds
-
Mc Garvey, G. J.; Stepanian, M. W.; Bressette, A. R.; Sabat, M. Design and synthesis of a new class of nonmacrocyclic alkali metal host compounds. Org. Lett. 2000, 2, 3453-3456.
-
(2000)
Org. Lett.
, vol.2
, pp. 3453-3456
-
-
Mc Garvey, G.J.1
Stepanian, M.W.2
Bressette, A.R.3
Sabat, M.4
-
11
-
-
33845953429
-
A Sakurai- Prins- Ritter sequence for the three-component diastereoselective synthesis of 4-amino tetrahydropyrans
-
Epstein, O. L.; Rovis, T. A Sakurai- Prins- Ritter sequence for the three-component diastereoselective synthesis of 4-amino tetrahydropyrans. J. Am. Chem. Soc. 2006, 128, 16480-16481.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 16480-16481
-
-
Epstein, O.L.1
Rovis, T.2
-
12
-
-
39349108559
-
K Stereoselective one-pot, three-component synthesis of 4-amidotetrahydropyran
-
Reddy, U. C; Raju, B. R.; Kumar, E. K. P.; Saikia, A. K Stereoselective one-pot, three-component synthesis of 4-amidotetrahydropyran. J. Org. Chem. 2008, 73, 1628-1630.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 1628-1630
-
-
Reddy, U.C.1
Raju, B.R.2
Kumar, E.K.P.3
Saikia, A.4
-
13
-
-
10044267850
-
Highly efficient chemoselective deprotection of O,O-acetals and O,O-ketals catalyzed by molecular iodine in acetone
-
Sun, J.; Dong, Y.; Wang, X.; Hu, Y. Highly efficient chemoselective deprotection of O,O-acetals and O,O-ketals catalyzed by molecular iodine in acetone. J. Org. Chem. 2004, 69, 8932-8934.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 8932-8934
-
-
Sun, J.1
Dong, Y.2
Wang, X.3
Hu, Y.4
-
14
-
-
2442701279
-
Iodine as an extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions
-
Phukan, P. Iodine as an extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions. Tetrahedron Lett. 2004, 45, 4785-4787.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 4785-4787
-
-
Phukan, P.1
-
15
-
-
13744259489
-
Preparation of bisindolylalkanes from N-tert-butanesulfinyl aldimines
-
Ke, B.; Qin, Y.; He, Q.; Huang, Z.; Wang, F. Preparation of bisindolylalkanes from N-tert-butanesulfinyl aldimines. Tetrahedron Lett. 2005, 46, 1751-1753.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 1751-1753
-
-
Ke, B.1
Qin, Y.2
He, Q.3
Huang, Z.4
Wang, F.5
-
16
-
-
17744376784
-
Iodine-catalyzed highly efficient Michael reaction of indoles under solvent-free condition
-
Banik, B. K.; Fernandez, M.; Alvarez, C. Iodine-catalyzed highly efficient Michael reaction of indoles under solvent-free condition. Tetrahedron Lett. 2005, 46, 2479-2482.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 2479-2482
-
-
Banik, B.K.1
Fernandez, M.2
Alvarez, C.3
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