Display options
Cite
Gade NR, Devendram V, Pal M, et al. IBX mediated reaction of β-enamino esters with allylic alcohols: a one pot metal free domino approach to functionalized pyridines. Chem Commun (Camb). 2013;49(72):7926-8doi: 10.1039/c3cc44274h.
Gade, N. R., Devendram, V., Pal, M., & Iqbal, J. (2013). IBX mediated reaction of β-enamino esters with allylic alcohols: a one pot metal free domino approach to functionalized pyridines. Chemical communications (Cambridge, England), 49(72), 7926-8. https://doi.org/10.1039/c3cc44274h
Gade, Narendar Reddy, et al. "IBX mediated reaction of β-enamino esters with allylic alcohols: a one pot metal free domino approach to functionalized pyridines." Chemical communications (Cambridge, England) vol. 49,72 (2013): 7926-8. doi: https://doi.org/10.1039/c3cc44274h
Gade NR, Devendram V, Pal M, Iqbal J. IBX mediated reaction of β-enamino esters with allylic alcohols: a one pot metal free domino approach to functionalized pyridines. Chem Commun (Camb). 2013 Sep 18;49(72):7926-8. doi: 10.1039/c3cc44274h. Epub 2013 Jul 30. PMID: 23900491.
Copy Download .nbib Format: NLM
Share it on

Chem Commun (Camb). 2013 Sep 18;49(72):7926-8. doi: 10.1039/c3cc44274h. Epub 2013 Jul 30.

IBX mediated reaction of β-enamino esters with allylic alcohols: a one pot metal free domino approach to functionalized pyridines.

Chemical communications (Cambridge, England)

Narendar Reddy Gade, V Devendram, Manojit Pal, Javed Iqbal

Affiliations

  1. Dr Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India. [email protected] [email protected].

PMID: 23900491 DOI: 10.1039/c3cc44274h

Abstract

IBX facilitated the reaction of β-enamino esters with allylic alcohols affording a direct, one-pot and metal free synthesis of functionalized pyridines including 2-substituted nicotinic acids, densely substituted pyridines and precursors of azafluorenones. The methodology also afforded the racemic pyridine core of cyclothiazomycin.

Publication Types