B.R. Maiti

Bio: B.R. Maiti is an academic researcher from University of Calcutta. The author has contributed to research in topics: Prolactin & Arecoline. The author has an hindex of 10, co-authored 27 publications receiving 268 citations.

Aryl-aryl bond formation by transition-metal-catalyzed direct arylation.

Abstract: The biaryl structural motif is a predominant feature in many pharmaceutically relevant and biologically active compounds. As a result, for over a century 1 organic chemists have sought to develop new and more efficient aryl -aryl bond-forming methods. Although there exist a variety of routes for the construction of aryl -aryl bonds, arguably the most common method is through the use of transition-metalmediated reactions. 2-4 While earlier reports focused on the use of stoichiometric quantities of a transition metal to carry out the desired transformation, modern methods of transitionmetal-catalyzed aryl -aryl coupling have focused on the development of high-yielding reactions achieved with excellent selectivity and high functional group tolerance under mild reaction conditions. Typically, these reactions involve either the coupling of an aryl halide or pseudohalide with an organometallic reagent (Scheme 1), or the homocoupling of two aryl halides or two organometallic reagents. Although a number of improvements have developed the former process into an industrially very useful and attractive method for the construction of aryl -aryl bonds, the need still exists for more efficient routes whereby the same outcome is accomplished, but with reduced waste and in fewer steps. In particular, the obligation to use coupling partners that are both activated is wasteful since it necessitates the installation and then subsequent disposal of stoichiometric activating agents. Furthermore, preparation of preactivated aryl substrates often requires several steps, which in itself can be a time-consuming and economically inefficient process.

Recent advances in aryl–aryl bond formation by direct arylation

Abstract: The abundance of the biaryl structural motif in natural products, in biologically active molecules and in materials chemistry has positioned aryl–aryl (Ar–Ar) bond formation high on the agenda of synthetic chemists. For decades well-known reactions such as the Mizoroki–Heck and Suzuki–Miyaura have been the methods of choice to furnish biaryls. More recently, however, alternative methods, most notably direct arylation via C–H activation, have become the focus of many research groups. Compared to traditional methods, direct arylation affords Ar–Ar compounds in fewer steps by removing the need for prefunctionalisation. Furthermore, given that either one or two hydrogens are targeted, less waste and good atom economy are features of this methodology. This critical review covers, in the main part, reports from January 1, 2006, to October 22, 2008 (117 references).

Histochemistry, Theoretical and Applied.

Abstract: municable disease control to the newer responsibilities of the hazards of ionizing radiation and medical defense against atomic attack. The individual topics are adequately developed with emphasis, in the majority, on brevity of presentation rather than complete and exhaustive detail. References are listed after each chapter for the reader desiring more definitive information. \"Epidemiologic Methods and Inferences\" by Dr. Dienfeld and \"Official and Voluntary Health Agencies\" by Dr. Hilleboe are two chapters which offer especially well-organized, succinct, and effective discussions of their respective subjects. The editors state in their preface that they are presenting \". . a new way to look at preventive medicine for the medical students, general practitioners, specialists, and professional workers in official and voluntary health agencies.\" In the opinion of the reviewer, the authors have achieved their purpose by editing a book which is more an introductory text than a reference tome.