Recent contributions from the Baylis− Hillman reaction to organic chemistry

D Basavaiah, BS Reddy, SS Badsara - Chemical reviews, 2010 - ACS Publications
Organic synthesis is one of the most successful and useful disciplines of science and mainly
involves the construction of carbon-carbon bond (s) and carbon-heteroatom bond (s) and …

aza-Baylis−Hillman Reaction

V Declerck, J Martinez, F Lamaty - Chemical Reviews, 2009 - ACS Publications
The creation of carbon-carbon bonds remains an important challenge in organic synthesis.
Numerous reactions for the formation of carbon-carbon bonds have been discovered and …

A facile and efficient synthesis of highly functionalised 3, 3′-dispiropyrrolidine-and 3, 3′-dispiropyrrolizidine bisoxindoles via [3+ 2] cycloaddition

P Shanmugam, B Viswambharan, K Selvakumar… - Tetrahedron …, 2008 - Elsevier
The [3+ 2] cycloaddition reaction of azomethine ylides with isomerised Morita–Baylis–
Hillman adducts, both dipoles and dipolarophiles are derived from isatin, afforded highly …

Stereoselective synthesis of 3-spiro-α-methylene-γ-butyrolactone oxindoles from Morita–Baylis–Hillman adducts of isatin

P Shanmugam, V Vaithiyanathan - Tetrahedron, 2008 - Elsevier
A concise stereoselective synthesis of 3-spiro-α-methylene-γ-butyrolactone oxindoles from
Morita–Baylis–Hillman adducts of isatin in excellent yield has been achieved following a …

A Short and Efficient Synthesis of 3-Spiro-α-methylene-γ-butyrolactone Oxindolones from Isomerised Bromo Derivatives of Morita-Baylis-Hillman Adducts

P Shanmugam, B Viswambharan - Synlett, 2008 - thieme-connect.com
A short and efficient synthesis of α-methylene-γ-butyrolactone-3-spirooxindolones by the
reaction of isomerised bromo derivatives of Morita-Baylis-Hillman adducts of isatin and …

A simple synthesis of ferrocenyl bis-amides by a Ugi four-component reaction

R Akbarzadeh, P Mirzaei, A Bazgir - Journal of Organometallic Chemistry, 2010 - Elsevier
A simple synthesis of ferrocenyl bis-amides by a Ugi four-component reaction - ScienceDirect
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Activated Alkene Dependent One-Pot, Three-Component Aza-Morita− Baylis− Hillman Reaction of Ferrocenealdehyde: Synthesis of Highly Functionalized Diverse …

S Madhavan, P Shanmugam - Organic Letters, 2011 - ACS Publications
Activated alkene dependent one-pot, three-component aza-Morita− Baylis− Hillman (aza-
MBH) reaction of ferrocenealdehyde afforded simple aza-MBH adduct of ferrocenealdehyde …

An efficient copper catalyzed one-pot, four-component, and diastereoselective synthesis of highly functionalized ferrocenyl azetidinimines

S Gouthaman, P Shanmugam, AB Mandal - Tetrahedron Letters, 2013 - Elsevier
An efficient, facile, and diastereoselective synthesis of highly functionalized ferrocenyl
azetidinimines from copper catalyzed one-pot, four-component reaction of …

Bipyridine carbaldehydes as electrophiles in the Morita–Baylis–Hillman reaction: synthesis of highly functionalized bipyridyl ligands and a macrocycle

S Gouthaman, S Periyaraja, P Shanmugam - Tetrahedron letters, 2015 - Elsevier
A simple and efficient Morita–Baylis–Hillman (MBH) reaction of bipyridine carbaldehydes
and unexplored activated alkenes afforded highly functionalized bipyridyl ligands …

Development of a mild and efficient protocol for the protection and O-alkylation of allyl alcohols

K Selvakumar, KAP Lingam, RVL Varma - RSC Advances, 2014 - pubs.rsc.org
An efficient, pyridine-free protocol has been developed for the protection of the 3°-allyl
alcohol of oxindole using a mild base, such as potassium carbonate, under microwave …