V. Anand

发表

STRUCTURAL CHARACTERIZATION OF MESO ARYL SAPPHYRINS

T. K. Chandrashekar, S. Pushpan, A. Srinivasan, 1999 .

Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.

V. Anand, Santosh C. Gadekar, B. Reddy, 2016, Chemical communications.

Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes.

V. Anand, Santosh C. Gadekar, B. Reddy, 2015, Chemical communications.

Porphyrins in photodynamic therapy - a search for ideal photosensitizers.

T. K. Chandrashekar, S. Ganesan, D. Parmeswaran, 2002, Current medicinal chemistry. Anti-cancer agents.

Inverted porphyrins and expanded porphyrins: An overview

T. K. Chandrashekar, S. Pushpan, J. Sankar, 2002 .

Porphyrins: Syntheses and Reactions

T. K. Chandrashekar, A. Srinivasan, V. Anand, 2011 .

Antiaromatic supramolecules: F···S, F···Se, and F···π intermolecular interactions in 32π expanded isophlorins.

Tullimilli Y. Gopalakrishna, V. Anand, J. Reddy, 2013, Angewandte Chemie.

Biscopper complexes of meso-aryl-substituted hexaphyrin: gable structures and varying antiferromagnetic coupling.

T. Yokoyama, A. Osuka, K. Furukawa, 2004, Journal of the American Chemical Society.

pi-Conjugated macrocycles from thiophenes and benzenes.

V. Anand, J. Sreedhar Reddy, 2008, Chemical communications.

Isophlorinoids: The Antiaromatic Congeners of Porphyrinoids.

V. Anand, B. Reddy, A. Basavarajappa, 2017, Chemical reviews.

Controlled Core-Modification of a Porphyrin into an Antiaromatic Isophlorin.

V. Anand, Santosh C. Gadekar, S. Panchal, 2016, Angewandte Chemie.

Planar meso pentafluorophenyl core modified isophlorins.

V. Anand, J. Reddy, 2008, Journal of the American Chemical Society.

Non-covalent composites of antiaromatic isophlorin-fullerene.

V. Anand, Santosh C. Gadekar, B. Reddy, 2015, Chemical communications.

A naphthalene-fused dimer of an anti-aromatic expanded isophlorin.

P. Kögerler, Jeff Rawson, V. Anand, 2017, Chemical communications.

Reversible redox reaction between antiaromatic and aromatic states of 32π-expanded isophlorins.

Tullimilli Y. Gopalakrishna, V. Anand, 2014, Angewandte Chemie.

Core modified oxybenziporphyrins: new aromatic ligands for metal-carbon bond activation.

T. K. Chandrashekar, S. Pushpan, J. Sankar, 2002, Chemical communications.

Non-planar core-modified dibenzi expanded isophlorin

V. Anand, Madan D Ambhore, Rakesh Gaur, 2020 .

Internally 1,4-phenylene-bridged meso aryl-substituted expanded porphyrins: the decaphyrin and octaphyrin cases.

A. Osuka, Soji Shimizu, Shohei Saito, 2005, Angewandte Chemie.

N-confused expanded porphyrin: first example of a modified sapphyrin with an inverted N-confused pyrrole ring.

T. K. Chandrashekar, S. Pushpan, A. Srinivasan, 2001, Journal of the American Chemical Society.

"To Twist or Not to Twist": Figure-of-Eight and Planar Structures of Octaphyrins.

Neelam Shivran, V. Anand, Santosh C. Gadekar, 2017, Chemistry, an Asian journal.

Metal-assisted cyclomerization of N-confused dipyrrins into expanded norroles.

V. Anand, Santosh C. Gadekar, B. Reddy, 2013, Angewandte Chemie.

An amphoteric switch to aromatic and antiaromatic states of a neutral air-stable 25π radical.

Tullimilli Y. Gopalakrishna, V. Anand, J. Reddy, 2014, Angewandte Chemie.

The synthesis and characterization of the meso-meso linked antiaromatic tetraoxa isophlorin dimer.

V. Anand, Santosh C. Gadekar, B. Reddy, 2016, Chemical communications.

Core modified meso-aryl sapphyrins and rubyrins: structural and anion receptor properties

T. K. Chandrashekar, S. Pushpan, A. Srinivasan, 2000 .

A wide-range of redox states of core-modified expanded porphyrinoids.

V. Anand, A. Basavarajappa, Madan D Ambhore, 2019, Chemical communications.

34pi octaphyrin: first structural characterization of a planar, aromatic [1.0.1.0.1.0.1.0] octaphyrin with inverted heterocyclic rings.

T. K. Chandrashekar, A. Dey, S. Pushpan, 2001, Journal of the American Chemical Society.

Syntheses and Redox Chemistry of Antiaromatic Core-Modified Isophlorinoids

V. Anand, B. Reddy, S. Panchal, 2018, Synlett.

Cyclic oligofurans: one-pot synthesis of 30pi and 40pi expanded porphyrinoids.

S. Mandal, V. Anand, J. Reddy, 2006, Organic letters.

Aromatic expanded isophlorins: stable 30pi annulene analogues with diverse structural features.

V. Anand, J. Reddy, 2009, Journal of the American Chemical Society.

Three dimensional isophlorinoid tetrapodal molecular cage.

V. Anand, A. Basavarajappa, Madan D Ambhore, 2021, Chemical communications.

Symmetric 32π (1.0.1.0.1.0.1) Core-Modified Heptaphyrins from Asymmetric Building Block.

Prachi Gupta, V. Anand, 2021, Organic letters.

Oxidative Transformation of a Tetrathia S-Confused Isophlorin into Porphyrin Cation.

V. Anand, S. Panchal, 2017, Organic letters.

Cyclic Oligofurans: One-Pot Synthesis of 30π and 40π Expanded Porphyrinoids.

S. Mandal, V. Anand, J. Reddy, 2007 .

Two-electron Oxidation of a Twisted Non Anti-aromatic 40π Expanded Isophlorin

Prachi Gupta, V. Anand, S. Panchal, 2016, Journal of Chemical Sciences.

Core-modified hexaphyrins; characterization of two- and four-ring inverted 26 pi aromatic macrocycles.

T. K. Chandrashekar, C. Khetrapal, U. Schilde, 2003, Organic letters.

30π Aromatic Meso-Substituted Heptaphyrin Isomers: Syntheses, Characterization, and Spectroscopic Studies

T. K. Chandrashekar, A. Dey, S. Pushpan, 2002 .

meso-Substituted Aromatic 34π Core-Modified Octaphyrins: Syntheses, Characterization and Anion Binding Properties.

T. K. Chandrashekar, H. Rath, K. Ruhlandt-Senge, 2003 .

meso-substituted aromatic 34pi core-modified octaphyrins: syntheses, characterization and anion binding properties.

T. K. Chandrashekar, H. Rath, K. Ruhlandt-Senge, 2003, Chemistry.

Characterization of a new meso-aryl rubyrin isomer: [26]hexaphyrin (1.1.1.0.1.0) with an inverted heterocyclic ring

T. K. Chandrashekar, A. Srinivasan, V. Anand, 2001 .

Tailoring diradicaloid properties of expanded isophlorinoids with systematic core-modification.

R. Gonnade, V. Anand, Pragati Shukla, 2022, Chemical Communications.