Iodine-catalyzed tandem synthesis of terminal acetals and glycol mono esters from olefins

Chemical Communications

Volumn 49, Issue 17, 2013, Pages 1711-1713

  Kumar, Macharla Arun ^a   Swamy, Peraka ^a   Naresh, Mameda ^a   Reddy, Marri Mahender ^a   Rohitha, Chozhiyath Nappunni ^a   Prabhakar, Sripadi ^a   Sarma, Akella Venkata Subrahmanya ^a   Kumar, Joseph Richard Prem ^a   Narender, Nama ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL DERIVATIVE; ALKENE DERIVATIVE; ESTER DERIVATIVE; GLYCOL MONO ESTER; IODINE; REAGENT; SODIUM PEROXIDE; UNCLASSIFIED DRUG;

ACETALIZATION; ARTICLE; CATALYSIS; ONE POT SYNTHESIS; OXIDATION; REACTION ANALYSIS; ROOM TEMPERATURE;

EID: 84873322652     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c3cc38085h     Document Type: Article

References (22)

1. T. W. Greene and P. G. M. Wuts, Protecting Groups in Organic Synthesis, John Wiley and Sons, New York, 3rd edn, 1999
2. H. Fujioka, A. Goto, K. Otake, O. Kubo, Y. Sawamaz, T. Maegawa, Chem. Commun, 2011, 47, 9894
3. J. W. Barlow, A. P. McHugh, O. Woods, J. J. Walsh, Eur. J. Med. Chem, 2011, 46, 1545
4. T. Ohta, T. Michibata, K. Yamada, R. Omori, I. Furukawa, Chem. Commun, 2003, 1192
5. Y.-J. Zhang, W. Dayoub, G.-R. Chen, M. Lemaire, Green Chem, 2011, 13, 2737
6. M. Curini, F. Epifano, M. C. Marcotullio, O. Rosati, Synlett, 1999, 777
7. W. Panchan, S. Chiampanichayakul, D. L. Snyder, S. Yodbuntung, M. Pohmakotr, V. Reutrakul, T. Jaipetch, C. Kuhakarn, Tetrahedron, 2010, 66, 2732
8. J. Tsuji, Palladium Reagents and Catalysts Innovations in Organic Synthesis, John Wiley & Sons, New York, 1998
9. D. F. Hunt, G. T. Rodeheaver, Tetrahedron Lett, 1972, 13, 3595
10. W. G. Lloyd, B. J. Luberoff, J. Org. Chem, 1969, 34, 3949
11. A. M. Balija, K. J. Stowers, M. J. Schultz, M. S. Sigman, Org. Lett, 2006, 8, 1121
12. M. Yamamoto, S. Nakaoka, Y. Ura, Y. Kataoka, Chem. Commun, 2012, 48, 1165
13. A. Kishi, S. Sakaguchi, Y. Ishii, Org. Lett, 2000, 2, 523
14. T. Hosokawa, T. Ohta, S.-I. Murahashi, J. Chem. Soc, Chem. Commun, 1983, 848
15. T. Hosokawa, T. Ohta, S. Kanayama, S.-I. Murahashi, J. Org. Chem, 1987, 52, 1758
16. F. Alonso, D. Sanchez, T. Soler, M. Yus, Adv. Synth. Catal, 2008, 350, 2118
17. P. M. Tadross, P. Bugga, B. M. Stoltz, Org. Biomol. Chem, 2011, 9, 5354
18. A. D. Chowdhury, G. K. Lahiri, Chem. Commun, 2012, 48, 3448
19. M. Ochiai, K. Miyamoto, M. Shiro, T. Ozawa, K. Yamaguchi, J. Am. Chem. Soc, 2003, 125, 13006
20. M. S. Yusubov, G. A. Zholobova, Russ. J. Org. Chem, 2001, 37, 1179
21. G. Lente, J. Kalmar, Z. Baranyai, A. Kun, I. Kek, D. Bajusz, M. Takacs, L. Veres, I. Fabian, Inorg. Chem, 2009, 48, 1763
22. B. R. Travis, M. Sivakumar, G. O. Hollist, B. Borhan, Org. Lett, 2003, 5, 1031