A Simple and Efficient Method for Transesterification of β-Ketoesters Catalysed by Iodine

Subhash P. Chavan; Ramesh R. Kale; K. Shivasankar; Sanjay I. Chandake; Swapnanjali B. Benjamin

doi:10.1055/s-2003-42433

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Synthesis 2003(17): 2695-2698
DOI: 10.1055/s-2003-42433

PAPER

A Simple and Efficient Method for Transesterification of β-Ketoesters Catalysed by Iodine

Subhash P. Chavan*, Ramesh R. Kale, K. Shivasankar, Sanjay I. Chandake, Swapnanjali B. Benjamin
Division of Organic Chemistry Technology, National Chemical Laboratory, Pune- 411 008, India
Fax: +91(20)5893614; e-Mail: spchavan@dalton.ncl.res.in;

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Publication History

Received 3 July 2003
Publication Date:
14 October 2003 (online)

Abstract
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Abstract

A facile transesterification of β-ketoesters using catalytic iodine is described.

Key words

transesterification - β-ketoesters - iodine - alcohols

References

1 Bader AR. Cummings LO. Vogel HA. J. Am. Chem. Soc. 1951, 73: 4195

Crossref Google Scholar
2 Gianotti M. Martelli G. Spunta G. Campana E. Panunzio M. Mendozza M. Synth. Commun. 2000, 30: 1725

Crossref Google Scholar
3 Mottet C. Hamelin O. Garavel G. Depres J. Greene AE. J. Org. Chem. 1999, 64: 1380

Crossref Google Scholar
4 Witzeman JS. Nottingham WD. J. Org. Chem. 1991, 56: 1713

Crossref Google Scholar
5 Taber DF. Amedio JC. Patel YK. J. Org. Chem. 1985, 50: 3618

Crossref Google Scholar
6 Seebach D. Thaler A. Blaser D. Ko SY. Helv. Chim. Acta 1991, 74: 1102

Crossref Google Scholar
7 Seebach D. Hungerbhler E. Naef R. Schnurrenberger D. Weidmann B. Zügger M. Synthesis 1982, 138

Article in Thieme Connect Google Scholar
8 Otera J. Yano T. Kawabata A. Hitoshi N. Tetrahedron Lett. 1986, 27: 2383

Crossref Google Scholar
9 Otera J. Dan-ho N. Nozaki H. J. Org. Chem. 1991, 56: 5307

Crossref Google Scholar
10 Rehberg CE. Fischer CH. J. Am. Chem. Soc. 1944, 66: 1203

Crossref Google Scholar
11 Chavan SP. Zubaidha PK. Dantale SW. Keshavaraja A. Ramamswamy AV. Ravindranathan T. Tetrahedron Lett. 1996, 37: 233

Crossref Google Scholar
12 Chavan SP. Rao TS. Dantale SW. Sivappa R. Synth. Commun. 2001, 31: 289

Crossref Google Scholar
13a Balaji BS. Sasidharan M. Kumar R. Chanda B. Chem. Commun. 1996, 707

Article in Thieme Connect Google Scholar
13b Balaji BS. Chanda BM. Tetrahedron 1998, 54: 13237

Article in Thieme Connect Google Scholar
13c Bandgar BP. Uppalla LS. Sadavarte VS. Green Chem. 2001, 3: 39

Article in Thieme Connect Google Scholar
13d Bandgar BP. Sadavarte VS. Uppalla LS. J. Chem. Res., Synop. 2001, 16

Article in Thieme Connect Google Scholar
13e Kumar P. Pandey RK. Synlett 2000, 251

Article in Thieme Connect Google Scholar
13f Christoffers J. Onal N. Eur. J. Org. Chem. 2000, 1633

Article in Thieme Connect Google Scholar
13g Bandgar BP. Uppalla LS. Sadavarte VS. Synlett 2001, 1715

Article in Thieme Connect Google Scholar
14 Ponde DE. Deshpande VH. Bulbule VJ. Sudalai A. Gajare AS. J. Org. Chem. 1998, 63: 1058

Crossref Google Scholar
15 Ranu BC. Dutta P. Sarkar A. J. Chem. Soc., Perkin 1 2000, 2223

Crossref Google Scholar
16 Olah GA. Narang SC. Saleom GF. Balaram Gupta BG. Synthesis 1981, 142

Article in Thieme Connect Google Scholar
17 Ramalinga K. Vijayalakshmi P. Kaimal TNB. Tetrahedron Lett. 2002, 43: 879

Crossref Google Scholar
18 Chavan SP. Shivasankar K. Sivappa R. Kale RR. Tetrahedron Lett. 2002, 43: 8583

Crossref Google Scholar
19 von Luttringhaus A. Prinzbach H. Liebigs Ann. Chem. 1959, 624: 79

Crossref Google Scholar