Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 2004(14): 2642-2643
DOI: 10.1055/s-2004-834833
DOI: 10.1055/s-2004-834833
SPOTLIGHT
© Georg Thieme Verlag Stuttgart · New York
Molecular Iodine
Further Information
Publication History
Publication Date:
20 October 2004 (online)
Introduction
The use of molecular iodine in organic synthesis has been known for a long time, such as in the Grignard reaction. In recent years, molecular iodine has received considerable attention as an inexpensive, non-toxic, readily available catalyst for various organic transformations under very mild and convenient conditions to afford the corresponding products in excellent yields with high selectivity. This is because of the mild Lewis acidity of iodine.
- 1
Kumar HMS.Reddy BVS.Reddy EJ.Yadav JS. Chem. Lett. 1999, 857 - 2
Nabajyoti D.Jadab CS. Synth. Commun. 2000, 30: 4435 - 3
Nabajyoti D.Jadab CS. J. Org. Chem. 2001, 66: 1947 - 4
Karimi B.Golshani B. J. Org. Chem. 2000, 65: 7228 - 5
Firouzabadi H.Iranpoor N.Sobhani S. Tetrahedron Lett. 2002, 43: 3653 - 6
Samajdar S.Basu MK.Becker FF.Banik BK. Tetrahedron Lett. 2001, 42: 4425 - 7
Nabajyoti D.Sarma JC. Chem. Lett. 2001, 794 - 8
Nabajyoti D.Dipok JK.Ruli B.Sarma JC. J. Org. Chem. 1997, 62: 1563 -
9a
Capaccio CI.Varela O. J. Org. Chem. 2002, 67: 7839 -
9b
Yadav JS.Reddy BVS.Rao CV.Chand PK.Prasad AR. Synlett 2001, 1638 -
9c
Yadav JS.Reddy BVS.Rao CV.Reddy MS. Synthesis 2003, 247 - 10
Yadav JS.Reddy BVS.Sadasiv K.Satheesh G. Tetrahedron Lett. 2002, 43: 9695 - 11
Wang S.-Y.Ji S.-J.Loh T.-P. Synlett 2003, 2377 - 12
Yadav JS.Reddy BVS.Rao CV.Rao KV. J. Chem. Soc., Perkin Trans. 1 2002, 11: 1401 -
13a
Bandgar BP.Shaikh KA. Tetrahedron Lett. 2003, 44: 1959 -
13b
Ji S.-J.Wang S.-Y.Loh T.-P. Tetrahedron 2004, 60: 2051 - 14
Banik BK.Samajdar S.Banik I. J. Org. Chem. 2004, 69: 213