Flow Chemistry India 2016, 21-22 January 2016, Mumbai, India

Flow Chemistry India 2016 Date: Thursday, 21 January 2016 - Friday, 22 January 2016 Location: Mumbai, India

SELECTBIO INDIA 
http://selectbiosciences.com/conferences/index.aspx?conf=FCINDIA16&se=india


Register..............http://selectbiosciences.com/conferences/registration.aspx?conf=FCINDIA16&se=india

venue
 Hotel Ramada Powai and Convention Centre, Mumbai, India

• Home, 
• Registration
• Exhibition
• |Venue
• |Media
• |Short Courses
• |Posters
• |Keynote Speakers

Paul Watts Professor & Research Chair, Nelson Mandela Metropolitan University

Shu Kobayashi Professor, Synthetic Organic Chemistry , The University of Tokyo

Vivek Ranade Deputy Director and Chair, National Chemical Laboratory

Volker Hessel Professor, Eindhoven University of Technology

Claude de Bellefon Scientific Director, University of Lyon

Marek Trojanowicz Professor, University of Warsaw

Ferenc Darvas Chairman, Flow Chemistry Society YOUR ORGANISERS  SANJAY BAJAJ MD, SELECTBIO Pooja Sharma and Sakshi Modgil, Garima Sharma

 Maninderjit Singh Ahluwalia

 

 Jayshree Select Bio

 

Overview

SELECTBIO INDIA is delighted to welcome you all at the 4th International Conference Flow Chemistry India 2016 to be held in Mumbai on January 21-22, 2016 under the auspices of the Flow Chemistry Society.  The society aims to unite and represent those who are actively working on this rapidly developing field. This meeting is dedicated to the integration of flow chemistry into everyday practice throughout the world by delivering the latest knowledge and making it available for the entire chemistry community.

Society members save 25% on the registration fee and non-members will receive their first year's membership included in the fee.

Running alongside the conference will be an exhibition covering the latest technological advances in the area of flow chemistry.

Who Should Attend
• Scientists, Chemists, Chemical Engineers and Researchers working in Pharmaceutical and Fine Chemicals Research and Development including Drug Discovery, Medicinal Chemistry and Chemical Process Development
• Scientists, Chemists and Chemical Engineers working in Pharmaceutical and Fine Chemical Bulk Manufacturing Units
• Corporate Management, Scientists, Managers responsible for development of Pharmaceutical and Fine Chemicals R & D and Manufacturing activities
• Scientists, Chemists & Engineers belonging to the fields of Inorganic, Organic, Medicinal, Natural Products, Analytical, High-throughput and Process Chemistry in the Academic research as well as in Applied research and development in the area of Agrochemical, Petrochemical and Fragrance industry
• Scientists working in or interested in applications of Flow Chemistry in Material science, Green chemistry, Nanotechnology, Biotechnology, Theoretical Chemistry, Information technology and Flow synthesis instruments including Engineering & Automation

Conference Package - Includes Registration, 2 Nights Accommodation, Dinner & Airport Transfers (Valid up to January 5, 2016 only)
 

Call for Posters

You can also present your research on a poster while attending the meeting. Submit an abstract for consideration now!

Poster Submission Deadline: 30 November 2015

Agenda Topics

• Advances in Micro & Continuous Flow Reactors, Systems & Processes
• Applications in Pharmaceutical Industry & API Synthesis
• Engineering Aspects of Flow Chemistry
• Flow Reactor - Choosing the Right One
• Photochemistry & Multistep Synthesis in Flow
• Quality Issue and QbD in Flow Chemistry
• Scale up - From Micro to Commercial Scale
• Yield Improvement, Cost Cutting and Waste Reduction in Flow Chemistry

Sponsorship and Exhibition Opportunities

Maninderjit Singh, Exhibition Manager
mjsingh@selectbio.com
7696225050

http://selectbiosciences.com/conferences/index.aspx?conf=FCINDIA16&se=india

214, Level 2, SCO 28-30, Sector 9D, Chandigarh, 160009, Indiap.sharma@selectbio.com

Mobile: +91 (0) 7696325050

Office:   +91 (0) 172 5025050

www.selectbio.com, www.selectbioindia.net

2015 conference and exhibition schedule

  
Workshop Tutor

Charlotte Wiles
CEO CHEMTRIX
 A Workshop on "Flow Chemistry Demonstrations (Lab & Plant Scale) for Chemical and Pharmaceutical Industry-" will be held one day prior to the training course i.e. on 20th January, 2016 from 10:00 am – 05:00 pm in Mumbai. This workshop is supported by Process Intensification will be jointly conducted by :

Dr. Dinesh Kudav (Mumbai University); Dr. Charlotte Wiles (Chemtrix BV-Neth);  Mr. Wouter Stam (Flowid, NV-Neth); Mr. Manjinder Singh (CIPLA & VP-FCS-India Chapter);  Dr. Viktor Gyollai, (AM Technology-UK);  Dr. Prashant Kini (UPL Ltd.); Mr. Kumar Oza (Pi & TCPL);  Mr. Madhav Sapre (Pi & Sharon Bio); et al .

This workshop is specially designed to demonstrate application/capabilities of  Flow Chemistry running “live” reactions in Continuous Flow Reactors. The reactions likely to be demonstrated using Flow Chemistry includes :• Nitration • Organometallic reaction• Oxidation • Bi-phasic reaction• Nano-Particle preparation in Flow• Biocatalytic Reaction with enhanced enzyme life.

This workshop is free for the registered delegates of Flow Chemistry India 2016 Conference and Continuous Flow Reactors Training Course.



You can visit Mumbai city


Taj hotel, mumbai

Gateway of india

Food in mumbai


 mumbai skyline



 The Bandra-Worli Sea Link is a cable-stayed bridge that connects central Mumbai with its western suburbs

 


 
 get in if you can

 The Mumbai Suburban Railway system carries more than 6.99 million commuters on a daily basis. It has the highest passenger densities of any urban railway ...


 

 

 Chhatrapati shivaji in mumbai india

British-victoria terminus



 

 



 VADA PAV



 

 


 



SELECTBIO CONFERENCES PICS






 

 

 
 
 

 MYSELF ON A WHEEL CHAIR IN PAST FLOW CHEMISTRY CONFERENCE IN MUMBAI
/////////

Aaron C. Sather

.

 Aaron C. Sather
 Buchwald Group
 Aaron is a NIH Postdoctoral Fellow at MIT in the research laboratory of Prof. Stephen Buchwald.

Contact Information

t: 617-253-8893
e: ASATHER@MIT.EDU

 https://chemistry-buchwald.mit.edu/people/aaron-c-sather
 https://www.linkedin.com/in/aaron-c-sather-943bba6a
https://www.researchgate.net/researcher/13844034_Aaron_C_Sather
http://www.epernicus.com/users/3325
https://www.facebook.com/aaron.c.sather


Aaron C. Sather earned his BSc at the University of Oregon, working with Prof. Darren W. Johnson on arsenic remediation and anion recognition. He graduated cum laude with the distinction of departmental honors. He then moved to The Scripps Research Institute to study molecular recognition under the guidance of Prof. Julius Rebek, Jr., where he was both a Baxter Fellow and an ARCS Fellow. Presently, Aaron is a NIH Postdoctoral Fellow at MIT in the research laboratory of Prof. Stephen Buchwald.

Lab Positions	Start Date	Fellowships and Awards	Previous Institutions
Postdoctoral Researcher	2013	NIH Postdoctoral Fellowship	Ph.D: The Scripps Research Institute, La Jolla, CA Advisor: Prof. Julius Rebek, Jr. Thesis: Molecular Encapsulation and the Selective Recognition of the Uranyl Ion B.Sc: University of Oregon, Eugene, OR Advisor: Prof. Darren W. Johnson Thesis: Anion Recognition and Arsenic Remediation

Experience

NIH post-doctoral fellow

Massachusetts Institute of Technology (MIT)

September 2013 – Present (2 years 3 months)cambridge, massachusetts

Graduate Stutent

Julius Rebek Jr. Laboratory

2008 – Present (7 years)The Scripps Research Institute

Undergraduate Research Assistant

Darren W. Johnson Laboratory

2005 – 2008 (3 years)University of Oregon

Publications

Diastereoselectivity in the Self-Assembly of As2L2Cl2 Macrocycles is Directed by the As-π Interaction(Link)

Inorganic Chemistry

September 20, 2007

The As−π interaction, in conjunction with reversible As−thiolate bond formation, is used to direct the self-assembly of dinuclear As2L2Cl2 (L = a dithiolate) macrocycles that exist as equilibrium mixtures of both syn and anti diastereomers. The diastereomeric excess of these self-assembly reactions is controlled in a predictable manner by prudent choice of different achiral, isomeric ligands. A...more

Solution Phase Measurement of Both Weak σ and C−H···X− Hydrogen Bonding Interactions in Synthetic Anion Receptors(Link)

Journal of the American Chemical Society

July 29, 2008

A series of tripodal receptors preorganize electron-deficient aromatic rings to bind halides in organic solvents using weak σ anion-to-arene interactions or C−H···X− hydrogen bonds. 1H NMR spectroscopy proves to be a powerful technique for quantifying binding in solution and determining the interaction motifs, even in cases of weak binding.

Anion Binding Induces Helicity in a Hydrogen Bonding Receptor: Crystal Structure of a 2,6-Bis(anilinoethynyl)pyrdinium Chloride(Link)

Crystal Growth and Design

September 2, 2009

The synthesis and solid-state of 2,6-bis(anilinoethynyl)pyridine amide 1 is presented. Neutral receptor 1 forms a polymeric chain through hydrogen bonds and π stacking in the solid state. Upon protonation, receptor 1 undergoes significant conformational rearrangement to hydrogen bond to Cl−, forming a helix (H1+Cl−). This rare example of anion-induced helicity is detailed in the solid state and...more

Synthesis of Novel Aryl-1,2-oxaxoles from Ortho-hydroxyaryloximes(Link)

Tetrahedron Letters

November 11, 2009

The reaction of ortho-hydroxyaryloximes with p-toluenesulfonyl chloride in the presence of an amine base efficiently generates the corresponding aryl-1,2-oxazole. Investigations revealed that solvent polarity greatly affected the rate of the reaction with faster rates observed in more polar solvents. The reaction proceeds to completion in only a few minutes in acetonitrile at room temperature, and...more

A Synthetic Receptor for Hydrogen-Bonding to Fluorines of Trifluoroborates(Link)

Chemical Communications

September 4, 2009

A tripodal receptor featuring three inwardly-directed hydrogen-bond donors binds covalently bound fluorine atoms of trifluoroborates through hydrogen-bonding.

Autocatalysis and Organocatalysis with Kemp’s Triacid Compounds(Link)

Heterocycles

August 20, 2010

Synthetic structures capable of autocatalysis based on molecular recognition – self-replication – were introduced nearly 20 years ago. These systems involved neither informational oligomers such as nucleic acids nor conditions that are generally regarded as prebiotic, but they revealed how self-complementary molecules could act as templates for their own formation and helped define the structure...more

Reactivity of N-nitrosoamides in Confined Spaces(Link)

Tetrahedron Letters

April 27, 2011

The thermal rearrangement of several N-nitrosoamides was studied by 1H NMR in the context of reversible encapsulation. The N-nitrosoamide guests were isolated from the bulk solvent in a hydrogen-bonded dimeric host capsule which prevented their rearrangement. The guests appear to be preserved in their ground state conformations by the pressure exerted by the host. The conformations of the free and...more

Selective Recognition and Extraction of the Uranyl Ion(Link)

Journal of the American Chemical Society

September 14, 2010

A tripodal receptor capable of extracting uranyl ion from aqueous solutions has been developed. At a uranyl concentration of 400 ppm, the developed ligand extracts 59% of the uranyl ion into the organic phase. The new receptor features three carboxylates that converge on the uranyl ion through bidentate interactions. Solution studies reveal slow exchange of the carboxylates on the NMR time scale....more

Supramolecular Architecture with a Cavitand – Capsule Chimera(Link)

Angewandte Chemie International Edition

January 18, 2011

Molecule-within-molecule complexes are widely used in supramolecular chemistry for studies of molecular recognition and catalysis. Self-assembled hosts isolate their guests from the bulk media and reveal unique molecular behaviors. An assembly that features well-differentiated and non-interacting binding sites stabilized through hydrogen-bonding interactions is described.

A Light Controlled Cavitand Wall Regulates Guest Binding(Link)

Chemical Communications

September 14, 2010

Here we report a cavitand with a photochemical switch as one of the container walls. The azo-arene switch undergoes photoisomerization when subjected to UV light producing a self-fulfilled cavitand. This process is thermally and photochemically reversible. The reported cavitand binds small molecules and these guests can be ejected from the cavitand through this photochemical process.

Design, Synthesis and Characterization of Self-Assembled As2L3 and Sb2L3 Cryptands(Link)

Dalton Transactions

July 28, 2011

The syntheses and X-ray crystal structures of six new self-assembled supramolecular As and Sb-containing cryptands are described. Analysis in the context of previously reported As2L3 and Sb2L3 cryptands reveals that small differences in ligand geometries result in significant differences in the helicity of the complexes and the stereochemistry of the metal coordination within the assembled...more

A Deep Cavitand with a Fluorescent Wall Functions as an Ion Sensor(Link)

Organic Letters

September 13, 2011

The synthesis and characterization of a deep cavitand bearing a fluorescent benzoquinoxaline wall is reported. Noncovalent host–guest recognition events are exploited to sense small charged molecules including acetylcholine. The cavitand also exhibits an anion dependent change in fluorescence that is used to differentiate halide ions in solution.

Switchable Catalysis with a Light Responsive Cavitand(Link)

Angewandte Chemie International Edition

September 8, 2011

A cavitand with an azobenzene wall adopts an introverted shape when irradiated with UV light. This conformation has been characterized in solution and the solid state and is used to control guest binding. By incorporating an organocatalyst guest, the rate of the Knoevenagel condensation is controlled with light.

Synthesis of Fused Indazole Ring Systems and Application to Nigeglanine Hydrobromide(Link)

Organic Letters

March 2, 2012

The single-step synthesis of fused tricyclic pyridazino[1,2-a]indazolium ring systems is described. Structural details revealed by crystallography explain the unexpected reactivity. The method is applied to the gram scale synthesis of nigeglanine hydrobromide.

Uranyl Ion Coordination with Rigid Aromatic Carboxylates and Structural Characterization of their Complexes(Link)

Chemical Communications

May 31, 2013

Uranyl complexes of rigid aromatic carboxylates were synthesized and their solid-state structures characterized by X-ray crystallography. The new ligands create cavities lined with endohedral functions to encapsulate the uranyl ion.

Pnictogen-Directed Synthesis of Discrete Disulfide Macrocycles(Link)

Chemical Communications

June 5, 2013

Cyclic disulfide macrocycles were rapidly synthesized cleanly and selectively from rigid dithiols via oxidation with iodine when activated by pnictogen additives (As and Sb). Macrocycles were confirmed by 1H-NMR spectrscopy and X-ray crystallography. A p-xylyl-based disulfide trimer and tetramer crystallized in hollow, stacked columns stabilized by intermolecular, sulfur…sulfur close contacts.
 

Education

The Scripps Research Institute

Doctor of Philosophy (PhD), Chemistry

2008 – 2013

University of Oregon

Bachelor of Applied Science (B.A.Sc.), Chemistry

2005 – 2008

Massachusetts Institute of Technology

Post-Doc, Chemistry

2013

• 
  

  Went to Ballard High School

  Class of 2002
• 
  

  Lives in Cambridge, Massachusetts

  From Seattle, Washington

Aaron C Sather

With Aaliyah and Lupita Sather.

 
 
Cambridge, Massachusetts

 

 

 

 
 

 

 

 

 
 
///////////

Navid Dastbaravardeh

.

 Navid Dastbaravardeh studied chemistry at the Ludwig Maximilian University of Munich (LMU, Germany) and received his diploma in 2008. He then moved to the Vienna University of Technology (VUT, Austria), where he completed his Ph.D. in Organic Chemistry under the supervision of Profs. Michael Schnürch and Marko D. Mihovilovic. Supported by an Erwin- Schrödinger Research Fellowship, he is currently pursuing postdoctoral research with Prof. Jin-Quan Yu at The Scripps Research Institute, focusing on palladium-catalyzed C-H bond-functionalization reactions.


 Department of Chemistry, The Scripps Research Institute (TSRI), 10550 N. Torrey Pines Road, La Jolla, CA 92037 (USA). E-mail: yu200@scripps.edu











////////////