Virtual Issue: Celebrating Organic and Inorganic Chemistry Published by Authors in India

Chemists in India are increasingly publishing cutting-edge organic and inorganic chemistry research, as evidenced by the substantial growth in submissions from authors in India over the last decade (up 173%) across five ACS Publications journals within the organic/inorganic portfolio ( ACS Catalysis, Inorganic Chemistry, Organic Letters Organometallics, The Journal of Organic Chemistry). In 2016, research from scientists in India accounted for 6.2% of all papers published in these five journals. Among the Associate Editors and Editorial Board members for these journals are ten researchers based in India.

This month, ACS is sponsoring the Indo-US Organometallic Chemistry Workshop, December 8-10 in Mumbai, India. ACS Publications will be the only publisher attending this exclusive event, which was co-organized by the Indian Institute of Science Bangalore, the Indian Institutes of Science Education and Research Kolkata, the Indian Institute of Technology Bombay, and the University of Utah. The event will be attended by Journal of the American Chemical Society Associate Editor Matthew S. Sigman of the University of Utah and The Journal of Organic Chemistry Associate Editor Debabrata Maiti of the Indian Institute of Technology Bombay, both of whom are on the event’s organizing committee. ACS Omega Managing Editor Deeksha Gupta will also attend.

The organizers, speakers, and attendees of this invitation-only event have strong connections to ACS Publications. Check out this Virtual Issue of important recent papers published in the five participating journals from select participants below. You can click on the participants’ names to see their full list of papers published with ACS Publications.

Celebrating Organic and Inorganic Chemistry Published by Authors in India

Bishma K. Patel

Base-Promoted Synthesis of Quinoline-4(1H)-thiones from o-Alkynylanilines and Aroyl Isothiocyanates
Org. Lett., 2017, 19 (22), pp 6128–6131
DOI: 10.1021/acs.orglett.7b02993

Mathew S. Sigman

Developing Comprehensive Computational Parameter Sets To Describe the Performance of Pyridine-Oxazoline and Related Ligands
ACS Catal., 2017, 7 (6), pp 4144–4151
DOI: 10.1021/acscatal.7b00739

Jitendra K. Bera

Acceptorless Dehydrogenation of Alcohols on a Diruthenium(II,II) Platform
Organometallics, 2016, 35 (10), pp 1505–1513
DOI: 10.1021/acs.organomet.6b00085

Christopher Uyeda

Dehydrogenative Transformations of Imines Using a Heterogeneous Photocatalyst
J. Org. Chem., 2017, 82(11), pp 5959–5965
DOI: 10.1021/acs.joc.7b00617

James P. Morken

Modular, Catalytic Enantioselective Construction of Quaternary Carbon Stereocenters by Sequential Cross-Coupling Reactions
Org. Lett., 2016, 18 (13), pp 3286–3289
DOI: 10.1021/acs.orglett.6b01580

Sundargopal Ghosh

Synthesis, Chemistry, and Electronic Structures of Group 9 Metallaboranes
Inorg. Chem., 2017, 56 (3), pp 1524–1533
DOI: 10.1021/acs.inorgchem.6b02626

Burjor Captain

Reversible Inter- and Intramolecular Carbon–Hydrogen Activation, Hydrogen Addition, and Catalysis by the Unsaturated Complex Pt(IPr)(SnBut3)(H)
Inorg. Chem., 2016, 55 (6), pp 2679–2681
DOI: 10.1021/acs.inorgchem.6b00048

Raghavan B. Sunoj

Exploring the Mechanism and Stereoselectivity in Chiral Cinchona-Catalyzed Heterodimerization of Ketenes
J. Org. Chem., Article ASAP
DOI: 10.1021/acs.joc.7b02517

Swadhin K. Mandal

A Highly Efficient Base-Metal Catalyst: Chemoselective Reduction of Imines to Amines Using an Abnormal-NHC-Fe(0) Complex
Organometallics201635 (17), pp 2930–2937
DOI: 10.1021/acs.organomet.6b00478

Moumita Majumdar

Mixed Ligated Tris(amidinate)dimolybdenum Complexes as Catalysts for Radical Addition of CCl4 to 1-Hexene: Leaving Ligand Lability Controls Catalyst Activity
Inorg. Chem.201756 (1), pp 634–644
DOI: 10.1021/acs.inorgchem.6b02525

Srinivasarao Arulananda Babu

Pd(II)-Catalyzed Arylation and Intramolecular Amidation of γ-C(sp3)–H Bonds: En Route to Arylheteroarylmethane and Pyrrolidone Rind Annulated Furan/Thiophene Scaffolds
J. Org. Chem.201782(14), pp 7123–7150
DOI: 10.1021/acs.joc.7b00582

Vadapalli Chandrasekhar

Stepwise Reversible Oxidation of N-Peralkyl-Substituted NHC–CAAC Derived Triazaalkenes: Isolation of Radical Cations and Dications
Org. Lett.201719 (20), pp 5605–5608
DOI: 10.1021/acs.orglett.7b02721

Alan S. Goldman

Alkyl-Aryl Coupling Catalyzed by Tandem Systems of Pincer-Ligated Iridium Complexes and Zeolites
ACS Catal.20166 (5), pp 2836–2841
DOI: 10.1021/acscatal.6b00149

Eluvathingal D. Jemmis

Approaches to Sigma Complexes via Displacement of Agostic Interactions: An Experimental and Theoretical Investigation
Organometallics201736 (15), pp 2736–2745
DOI: 10.1021/acs.organomet.7b00210

Dean Toste

Uncovering Subtle Ligand Effects of Phosphines Using Gold(I) Catalysis
ACS Catal.20177 (6), pp 3973–3978
DOI: 10.1021/acscatal.7b00757

Sayam Sen Gupta

Iron Complex Catalyzed Selective C–H Bond Oxidation with Broad Substrate Scope
Org. Lett.201719 (4), pp 746–749
DOI: 10.1021/acs.orglett.6b03359

Sarah E. Reisman

Enantioselective Synthesis of (–)-Acetylapoaranotin
Org. Lett.201719 (7), pp 1698–1701
DOI: 10.1021/acs.orglett.7b00418

Akhila K. Sahoo

Regioselective Synthesis of 2,4,5-Trisubstituted Oxazoles and Ketene Aminals via Hydroamidation and Iodo-Imidation of Ynamides
J. Org. Chem.201782(19), pp 10583–10594
DOI: 10.1021/acs.joc.7b02124

Uttam K. Tambar

Catalytic Asymmetric Intermolecular Allylic Functionalization of Unactivated Internal Alkenes
ACS Catal.20177 (12), pp 8533–8543
DOI: 10.1021/acscatal.7b03081

Masilamani Jeganmohan

Ruthenium-Catalyzed ortho Alkenylation of Aromatics with Alkenes at Room Temperature with Hydrogen Evolution
ACS Catal.20166 (1), pp 230–234
DOI: 10.1021/acscatal.5b02218

Debabrata Maiti

Palladium-Catalyzed Remote meta-Selective C–H Bond Silylation and Germanylation
Organometallics201736 (13), pp 2418–2423
DOI: 10.1021/acs.organomet.7b00309

Ekambaram Balaraman

Expedient Cobalt-Catalyzed C–H Alkynylation of (Enantiopure) Benzylamines
Org. Lett.201618 (20), pp 5252–5255
DOI: 10.1021/acs.orglett.6b02549

Ajay Venugopal

Consequence of Ligand Bite Angle on Bismuth Lewis Acidity
Inorg. Chem.201756 (16), pp 9391–9395
DOI: 10.1021/acs.inorgchem.7b01243

Ashoka G. Samuelson

Computational Study of the Migration of Rhenium from One Enantioface of an Olefin to the Other Facilitated by (C–H)···Re Interactions
Organometallics201332 (23), pp 7141–7152
DOI: 10.1021/om400857n

Connie C. Lu

Redox Pairs of Diiron and Iron–Cobalt Complexes with High-Spin Ground States
Inorg. Chem.201655 (19), pp 9725–9735
DOI: 10.1021/acs.inorgchem.6b01487

Sambasivarao Kotha

Synthesis of Intricate Fused N-Heterocycles via Ring-Rearrangement Metathesis
J. Org. Chem.201782(16), pp 8527–8535
DOI: 10.1021/acs.joc.7b01299

Vadapalli Chandrasekhar

Heterometallic Heptanuclear [Cu5Ln2] (Ln = Tb, Dy, and Ho) Single-Molecule Magnets Organized in One-Dimensional Coordination Polymeric Network
Inorg. Chem.201756 (23), pp 14612–14623
DOI: 10.1021/acs.inorgchem.7b02450

Kevin Brown

Synthesis of 1,3-Substituted Cyclobutanes by Allenoate-Alkene [2 + 2] Cycloaddition
J. Org. Chem.201681(17), pp 8050–8060
DOI: 10.1021/acs.joc.6b01446

Ganesan Mani

Single-Step Substitution of all the α, β-Positions in Pyrrole: Choice of Binuclear versus Multinuclear Complex of the Novel Polydentate Ligand
Inorg. Chem.201453 (8), pp 4117–4129
DOI: 10.1021/ic5000974

Balaji R. Jagirdar

Implication of a σ-Methane Complex en Route to Elimination of Methane from a Ruthenium Complex: An Experimental and Theoretical Investigation
Organometallics201534 (7), pp 1245–1254
DOI: 10.1021/om501248v

Joyanta Choudhury

Dramatic Effect of Ancillary NHC Ligand in the Highly Selective Catalytic Oxidative Carbon–Carbon Multiple Bond Cleavage
Organometallics201635 (15), pp 2462–2466
DOI: 10.1021/acs.organomet.6b00337

Basker Sundararaju

Cp*Co(III)-Catalyzed C(sp3)–H Bond Activation: A Highly Stereoselective and Regioselective Alkenylation of 8-Methylquinoline with Alkynes
ACS Catal.20166 (5), pp 2792–2796
DOI: 10.1021/acscatal.6b00612

If you have comments or questions for the author of this post, please e-mail: Axial@acs.org.