-
1
-
-
0035944150
-
-
2O). Tetrahedron, 2001, 57, 8333-8337.
-
2O). Tetrahedron, 2001, 57, 8333-8337.
-
-
-
-
2
-
-
33746639198
-
A facile, catalytic and environmentally benign method for esterification of carboxylic acids and transesterification of carboxylic esters with nearly equimolar amounts of alcohols
-
Bose, D. S.; Satyender, A.; Rudra Das, A. P.; Hari Babu, M. A facile, catalytic and environmentally benign method for esterification of carboxylic acids and transesterification of carboxylic esters with nearly equimolar amounts of alcohols. Synthesis 2006, 2392-2396.
-
(2006)
Synthesis
, pp. 2392-2396
-
-
Bose, D.S.1
Satyender, A.2
Rudra Das, A.P.3
Hari Babu, M.4
-
3
-
-
0035903945
-
-
2O): A mild and efficient catalyst for deprotection of dioxolanes and trisilylethers. Tetrahedron Lett. 2001, 42, 6771-6774.
-
2O): A mild and efficient catalyst for deprotection of dioxolanes and trisilylethers. Tetrahedron Lett. 2001, 42, 6771-6774.
-
-
-
-
4
-
-
0141854090
-
Simple, economical, and environmentally benign selective regeneration of carbonyl compounds from oximes and N,N-dimethyl hydrazones
-
Bose, D. S.; Narasimha Reddy, A. V.; Rudra Das, A. P. Simple, economical, and environmentally benign selective regeneration of carbonyl compounds from oximes and N,N-dimethyl hydrazones. Synthesis 2003, 1883-1885.
-
(2003)
Synthesis
, pp. 1883-1885
-
-
Bose, D.S.1
Narasimha Reddy, A.V.2
Rudra Das, A.P.3
-
5
-
-
33746014047
-
Water-tolerant and reusable catalyst for the one-pot synthesis of dihydropyrimidin-2(1H)-ones under solvent free conditions
-
Bose, D. S.; Venu Chary, M.; Rudra Das, A. P.; Hari Babu, M. Water-tolerant and reusable catalyst for the one-pot synthesis of dihydropyrimidin-2(1H)-ones under solvent free conditions. Heterocycles 2006, 68, 1217-1224.
-
(2006)
Heterocycles
, vol.68
, pp. 1217-1224
-
-
Bose, D.S.1
Venu Chary, M.2
Rudra Das, A.P.3
Hari Babu, M.4
-
6
-
-
33744938147
-
High-yielding microwave assisted synthesis of quinoline and dihydroquinoline derivatives under solvent free conditions
-
Bose, D. S.; Kishore Kumar, R. High-yielding microwave assisted synthesis of quinoline and dihydroquinoline derivatives under solvent free conditions. Heterocycles 2006, 68, 549-559.
-
(2006)
Heterocycles
, vol.68
, pp. 549-559
-
-
Bose, D.S.1
Kishore Kumar, R.2
-
8
-
-
34249329620
-
40): A mild and efficient reusable catalyst for synthesis of aryl-14H-dibezo[a.j] xanthenes under conventional heating and microwave irradiation
-
40): A mild and efficient reusable catalyst for synthesis of aryl-14H-dibezo[a.j] xanthenes under conventional heating and microwave irradiation. Catal. Commun. 2007, 8, 1173-1177.
-
(2007)
Catal. Commun
, vol.8
, pp. 1173-1177
-
-
Nagarapu, L.1
Srinivas, K.2
Venu Chary, M.3
Satyender, A.4
-
9
-
-
34548676421
-
40): A mild and efficient reusable catalyst for synthesis of amidoalkyl naphthols in solution and under solvent-free conditions
-
40): A mild and efficient reusable catalyst for synthesis of amidoalkyl naphthols in solution and under solvent-free conditions. Catal. Commun. 2007, 8, 1729-1734.
-
(2007)
Catal. Commun
, vol.8
, pp. 1729-1734
-
-
Nagarapu, L.1
Baseeruddin, M.2
Satyender, A.3
Srinivas, K.4
-
10
-
-
0034722988
-
Total synthesis of leucascandrolide A
-
(a) Hoenberer, K. R.; Hamblet, C. L.; Leighton, J. L. Total synthesis of leucascandrolide A. J. Am. Chem. Soc. 2000, 122, 12894-12895;
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 12894-12895
-
-
Hoenberer, K.R.1
Hamblet, C.L.2
Leighton, J.L.3
-
11
-
-
0037020381
-
-
17, 18 Z isomers. Angew. Chem. Int. Ed. 2002, 41, 3701-3704.
-
17, 18 Z isomers. Angew. Chem. Int. Ed. 2002, 41, 3701-3704.
-
-
-
-
12
-
-
0030924784
-
Asymmetric synthesis of amines by nucleophilic 1,2-addition of organometallic reagents to the CN-double bond
-
(a) Enders, R. D.; Reinhold, U. Asymmetric synthesis of amines by nucleophilic 1,2-addition of organometallic reagents to the CN-double bond. Tetrahedron: Asymmetry 1997, 8, 1895-1946;
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 1895-1946
-
-
Enders, R.D.1
Reinhold, U.2
-
13
-
-
0038106171
-
Additions of organometallic reagents to C=N bonds: Reactivity and selectivity
-
(b) Bloch, R. Additions of organometallic reagents to C=N bonds: Reactivity and selectivity. Chem. Rev. 1998, 98, 1407-1438.
-
(1998)
Chem. Rev
, vol.98
, pp. 1407-1438
-
-
Bloch, R.1
-
14
-
-
1242307334
-
-
2O-NaI system as a Lewis acid. J. Org. Chem. 2004, 69, 1290-1297;
-
2O-NaI system as a Lewis acid. J. Org. Chem. 2004, 69, 1290-1297;
-
-
-
-
15
-
-
11844257601
-
Rhenium complex-catalyzed allylation of aldehydes with allyltributylstannane
-
(b) Nishiyama, Y.; Kakushou, F.; Sonoda, N. Rhenium complex-catalyzed allylation of aldehydes with allyltributylstannane. Tetrahedron Lett. 2005, 46, 787-789.
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 787-789
-
-
Nishiyama, Y.1
Kakushou, F.2
Sonoda, N.3
-
16
-
-
0037033229
-
Three component synthesis of homoallylic amines: Efficient catalysis by lanthanum triflate/benzoic acid
-
(a) Aspinall, H. C.; Bissett, J. S.; Greeves, N.; Levin, D. Three component synthesis of homoallylic amines: Efficient catalysis by lanthanum triflate/benzoic acid. Tetrahedron Lett. 2002, 43, 323-325;
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 323-325
-
-
Aspinall, H.C.1
Bissett, J.S.2
Greeves, N.3
Levin, D.4
-
17
-
-
0036012738
-
-
2O. J. Chem. Soc., Perkin Trans. 1, 2002, 1157-1158;
-
2O. J. Chem. Soc., Perkin Trans. 1, 2002, 1157-1158;
-
-
-
-
18
-
-
0037691713
-
Bmim] BF4 ionic liquid: A novel and recyclable reaction media for the synthesis of homoallylic amines
-
(d) Yadav, J. S.; Reddy, B. V. S.; Raju, A. K. [Bmim] BF4 ionic liquid: A novel and recyclable reaction media for the synthesis of homoallylic amines. Synthesis 2003, 883-886.
-
(2003)
Synthesis
, pp. 883-886
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Raju, A.K.3
-
19
-
-
33947279845
-
-
40): A mild and efficient reusable catalyst for one-pot synthesis of 1,2,4,5-tetra substituted imidazoles under conventional heating and microwave irradiation. J. Mol. Cat. A: Chem. 2007, 266, 104-108.
-
40): A mild and efficient reusable catalyst for one-pot synthesis of 1,2,4,5-tetra substituted imidazoles under conventional heating and microwave irradiation. J. Mol. Cat. A: Chem. 2007, 266, 104-108.
-
-
-
|