-
1
-
-
34447102708
-
A green chemistry approach to asymmetric catalysis: Solvent-free and highly concentrated reactions
-
DOI 10.1021/cr0509556
-
Walsh P. J. Li H. de Parrodi C. A. Chem. Rev. 2007, 107 (6), 2503. 10.1021/cr0509556 (Pubitemid 47029099)
-
(2007)
Chemical Reviews
, vol.107
, Issue.6
, pp. 2503-2545
-
-
Walsh, P.J.1
Li, H.2
Anaya De Parrodi, C.3
-
2
-
-
34447132417
-
Innovations and green chemistry
-
DOI 10.1021/cr078380v
-
Horváth I. T. Anastas P. T. Chem. Rev. 2007, 107 (6), 2169. 10.1021/cr078380v (Pubitemid 47033767)
-
(2007)
Chemical Reviews
, vol.107
, Issue.6
, pp. 2169-2173
-
-
Horvath, I.T.1
Anastas, P.T.2
-
4
-
-
0007264588
-
-
10.1021/cr960401q
-
Mizuno N. Misono M. Chem. Rev. 1998, 98 (1), 199. 10.1021/cr960401q
-
(1998)
Chem. Rev.
, vol.98
, Issue.1
, pp. 199
-
-
Mizuno, N.1
Misono, M.2
-
5
-
-
34547148003
-
Catalysts for Fine Chemical Synthesis
-
Derouane, E. Ed. Wiley: New York
-
Kozhevnikov, V. Catalysts for Fine Chemical Synthesis. Catalysis by Polyoxometalates; Derouane, E., Ed.; Vol. 2; Wiley: New York, 2002.
-
(2002)
Catalysis by Polyoxometalates
, vol.2
-
-
Kozhevnikov, V.1
-
6
-
-
14344263909
-
40) as a non-hygroscopic Lewis acid catalyst for the efficient Friedel-Crafts acylation of aromatic compounds under solvent-less conditions
-
DOI 10.1016/j.tet.2004.09.049
-
Firouzabadi H. Iranpoor N. Nowrouzi F. Tetrahedron 2004, 60 (48), 10843. 10.1016/j.tet.2004.09.049 (Pubitemid 40292267)
-
(2004)
Tetrahedron
, vol.60
, Issue.48
, pp. 10843-10850
-
-
Firouzabadi, H.1
Iranpoor, N.2
Nowrouzi, F.3
-
8
-
-
33744976601
-
A rapid and efficient method for 1,3-dithiolane synthesis
-
DOI 10.1016/j.tetlet.2006.05.057, PII S0040403906009828
-
Bez G. Gogoi D. Tetrahedron Lett. 2006, 47 (29), 5155. 10.1016/j.tetlet.2006.05.057 (Pubitemid 43867608)
-
(2006)
Tetrahedron Letters
, vol.47
, Issue.29
, pp. 5155-5157
-
-
Bez, G.1
Gogoi, D.2
-
11
-
-
0034247817
-
-
10.1021/cr000003u
-
a Marshall J. A. Chem. Rev. 2000, 100 (8), 3163. 10.1021/cr000003u
-
(2000)
Chem. Rev.
, vol.100
, Issue.8
, pp. 3163
-
-
Marshall, J.A.1
-
12
-
-
0003417469
-
-
Trost, B. M. Fleming, I. Heathcock, C. H. Eds. Pergamon: Oxford, UK
-
b Roush, W. R. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I.; Heathcock, C. H., Eds.; Pergamon: Oxford, UK. 1991; Vol. 2.
-
(1991)
Comprehensive Organic Synthesis
, vol.2
-
-
Roush, W.R.1
-
13
-
-
0346908681
-
-
Wiley-VCH: Weinheim, Germany
-
Hishashi, Y.; Koichiro, O. Main Group Metals in Organic Synthesis; Wiley-VCH: Weinheim, Germany, 2004; Vol. 2, pp. 621-720.
-
(2004)
Main Group Metals in Organic Synthesis
, vol.2
, pp. 621-720
-
-
Hishashi, Y.1
Koichiro, O.2
-
14
-
-
0038373087
-
Recent methods for the synthesis of (E)-alkene units in macrocyclic natural products
-
DOI 10.1002/anie.200301628
-
Prunet J. Angew. Chem. Int. Ed. 2003, 42 (25), 2826. 10.1002/anie. 200301628 (Pubitemid 36876596)
-
(2003)
Angewandte Chemie - International Edition
, vol.42
, Issue.25
, pp. 2826-2830
-
-
Prunet, J.1
-
15
-
-
29744452186
-
Stereoselective total synthesis of (+)-boronolide
-
DOI 10.1016/j.tet.2005.10.070, PII S0040402005019563
-
Boruwa J. Barua N. C. Tetrahedron 2006, 62 (6), 1193. 10.1016/j.tet.2005.10.070 (Pubitemid 43031309)
-
(2006)
Tetrahedron
, vol.62
, Issue.6
, pp. 1193-1198
-
-
Boruwa, J.1
Barua, N.C.2
-
16
-
-
38649100324
-
-
10.1016/j.tetlet.2007.12.113
-
Pospíšil J. Markó I. E. Tetrahedron Lett. 2008, 49 (9), 1523. 10.1016/j.tetlet.2007.12.113
-
(2008)
Tetrahedron Lett.
, vol.49
, Issue.9
, pp. 1523
-
-
Pospíšil, J.1
Markó, I.E.2
-
19
-
-
0043157642
-
-
10.1002/ejoc.200300099
-
Wang C.-J. Shi M. Eur. J. Org. Chem. 2003, 2003 (15), 2823. 10.1002/ejoc.200300099
-
(2003)
Eur. J. Org. Chem.
, vol.2003
, Issue.15
, pp. 2823
-
-
Wang, C.-J.1
Shi, M.2
-
22
-
-
0242497940
-
Chiral Bis-π-allylpalladium Complex Catalyzed Asymmetric Allylation of Imines: Enhancement of the Enantioselectivity and Chemical Yield in the Presence of Water
-
DOI 10.1021/ja037272x
-
Fernandes R. A. Stimac A. Yamamoto Y. J. Am. Chem. Soc. 2003, 125 (46), 14133. 10.1021/ja037272x (Pubitemid 37420918)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.46
, pp. 14133-14139
-
-
Fernandes, R.A.1
Stimac, A.2
Yamamoto, Y.3
-
23
-
-
0032770704
-
-
10.1002/(SICI)1099-0690(199901)1999:1<15: AID-EJOC15>3.0.CO;2-B
-
Kobayashi S. Eur. J. Org. Chem. 1999, 1999 (1), 15. 10.1002/(SICI)1099- 0690(199901)1999:1<15::AID-EJOC15>3.0.CO;2-B
-
(1999)
Eur. J. Org. Chem.
, vol.1999
, Issue.1
, pp. 15
-
-
Kobayashi, S.1
-
25
-
-
11844257601
-
Rhenium complex-catalyzed allylation of aldehydes with allyltributylstannane
-
DOI 10.1016/j.tetlet.2004.12.022, PII S0040403904026991
-
Nishiyama Y. Kakushou S. Sonoda N. Tetrahedron Lett. 2005, 46 (5), 787. 10.1016/j.tetlet.2004.12.022 (Pubitemid 40091673)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.5
, pp. 787-789
-
-
Nishiyama, Y.1
Kakushou, F.2
Sonoda, N.3
-
27
-
-
34250354060
-
Efficient allylation of aldehydes with allyltributylstannane catalyzed by CuI
-
DOI 10.1016/j.tetlet.2007.05.102, PII S0040403907009781
-
Kalita H. R. Borah A. J. Phukan P. Tetrahedron Lett. 2007, 48 (29), 5047. 10.1016/j.tetlet.2007.05.102 (Pubitemid 46921235)
-
(2007)
Tetrahedron Letters
, vol.48
, Issue.29
, pp. 5047-5049
-
-
Kalita, H.R.1
Borah, A.J.2
Phukan, P.3
-
28
-
-
11144342179
-
Chemoselective allylation of aldehydes using cerium(III) chloride: Simple synthesis of homoallylic alcohols
-
DOI 10.1016/j.tet.2004.11.029, PII S0040402004019015
-
Yadav J. S. Reddy B. V. S. Kondaji G. Reddy J. S. S. Tetrahedron 2005, 61 (4), 879. 10.1016/j.tet.2004.11.029 (Pubitemid 40037845)
-
(2005)
Tetrahedron
, vol.61
, Issue.4
, pp. 879-882
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Kondaji, G.3
Shyam Sunder Reddy, J.4
-
29
-
-
1242307334
-
2O-NaI System As A Lewis Acid
-
DOI 10.1021/jo035542o
-
Bartoli G. Bosco M. Giuliani A. Marcantoni E. Palmieri A. Petrini M. Sambri L. J. Org. Chem. 2004, 69 (4), 1290. 10.1021/jo035542o (Pubitemid 38233413)
-
(2004)
Journal of Organic Chemistry
, vol.69
, Issue.4
, pp. 1290-1297
-
-
Bartoli, G.1
Bosco, M.2
Giuliani, A.3
Marcantoni, E.4
Palmieri, A.5
Petrini, M.6
Sambri, L.7
-
31
-
-
33745714345
-
-
10.1021/jo060456k
-
Yao Q. Sheets M. J. Org. Chem. 2006, 71 (14), 5384. 10.1021/jo060456k
-
(2006)
J. Org. Chem.
, vol.71
, Issue.14
, pp. 5384
-
-
Yao, Q.1
Sheets, M.2
-
33
-
-
33644778560
-
Allylation of aldehydes and imines: Promoted by reuseable polymer-supported sulfonamide of N-glycine
-
DOI 10.1021/ol0528235
-
Li G.-l. Zhao G. Org. Lett. 2006, 8 (4), 633. 10.1021/ol0528235 (Pubitemid 43341977)
-
(2006)
Organic Letters
, vol.8
, Issue.4
, pp. 633-636
-
-
Li, G.-L.1
Zhao, G.2
-
34
-
-
3042807964
-
-
10.1023/B:CATL.0000030121.59482.6d
-
Sreekanth P. Park J. K. Kim J. W. Hyeon T. Kim B. M. Catal. Lett. 2004, 96 (3-4), 201. 10.1023/B:CATL.0000030121.59482.6d
-
(2004)
Catal. Lett.
, vol.96
, Issue.34
, pp. 201
-
-
Sreekanth, P.1
Park, J.K.2
Kim, J.W.3
Hyeon, T.4
Kim, B.M.5
-
39
-
-
79959254762
-
-
10.1016/j.tetlet.2011.05.050
-
Vanlaldinpuia K. Bez G. Tetrahedron Lett. 2011, 52 (29), 3759. 10.1016/j.tetlet.2011.05.050
-
(2011)
Tetrahedron Lett.
, vol.52
, Issue.29
, pp. 3759
-
-
Vanlaldinpuia, K.1
Bez, G.2
-
40
-
-
84856326558
-
-
The phrase "solvent-free conditions" is solely for the reaction only, not for purification of the products where solvents were used for purification by column chromatography
-
The phrase "solvent-free conditions" is solely for the reaction only, not for purification of the products where solvents were used for purification by column chromatography.
-
-
-
|