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Monday, 15 August 2016

Dr.Gowravaram Sabitha

  • Prof. Gowravaram Sabitha (CSIR-Indian Institute of Chemical Technology, Hyderabad, India)
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Sabitha Gowravaram

Sabitha Gowravaram


Senior Principal Scientist at Indian Institute of Chemical Technology

Dr. Gowravaram Sabitha
AddressScientist, Organic Division I, Indian Institute of Chemical Technology, Hyderabad-500 007, India
Phone number+91-40-27160512
Fax number+91-40-27160512
CountryIndia
Keywords
  • Custom synthesis
  • New chemical entities
  • New methodologies
  • Synthetic organic chemistry
  • Total synthesis of natutral products

Links


Total Stereoselective Synthesis and Structural Revision of a γ-Lactone Polyketide of Fungal Origin

Gowravaram Sabitha reports the stereoselective synthesis and structural revision of a γ-lactone polyketide of fungal origin.
Stereoselective Synthesis of the Revised Structure of γ-Lactone Polyketide from Diaporthe sp. SXZ-19 and Its C-8 Epimer: K. S. N. Reddy, A. Y. Reddy, G. Sabitha
Synthesis 201648, DOI: 10.1055/s-0035-1561463
A recently described γ-lactone polyketide originally isolated from the fungal strain Diaporthe sp. SXZ-19 of Camptotheca acuminata and its C-8 epimer were synthesized in stereoselective manner and their structure revised by Professor Gowravaram Sabitha and her colleagues from the CSIR-Indian Institute of Chemical Technology (Hyderabad, India).
  • Revised structures of polyketide γ-lactone and its C-8 epimer
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Professor Reddy – one of the article’s co-authors – said: “Synthesis of a γ-lactone polyketide has been achieved by utilizing Carreira, Ohira–Bestmann and alkyne–aldehyde coupling reactions.” 



LIST OF PUBLICATIONS 1. Synthesis of the C1-C25 Southern Domain of Spirastrellolides B and F. Gowravaram Sabitha,* Allu Senkara Rao and J. S. Yadav. Org & Biomol. Chem. 2013, 11, 7218-7231. 
2. Stereoselective formal synthesis of aspergillide A. Gowravaram Sabitha,* D. Vasudeva Reddy, Allu Senkara Rao and J. S. Yadav. Tetrahedron Lett. 2010, 51, 4195–4198. 
3. The First Stereoselective Total Synthesis of (−)-Synrotolide. Gowravaram Sabitha,* Allu Senkara Rao, AnkiReddy Sandeep and Jhillu S. Yadav. Eur. J. Org. Chem. 2013, accepted. 
4. Stereoselective synthesis of (−)-synparvolide B. Gowravaram Sabitha,* Allu Senkara Rao and J. S. Yadav. Tetrahedron: Asymmetry 2011, 22, 866-871. 
5. The First Total Synthesis of (−)-Synparvolide C. Gowravaram Sabitha,* AnkiReddy Sandeep, Allu Senkara Rao and J. S. Yadav. Eur. J. Org. Chem. 2013, accepted. 
6. Synthesis of the C1-C13 Subunit of Spirastrellolide A and B by Prins Cyclization. Gowravaram Sabitha,* Allu Senkara Rao and J. S. Yadav. Synthesis, 2010, 505-509. 
7. International Application published Under The Patent Cooperation Treaty (PCT). Process For The Preparation Of ASENAPINE Intermediate. Inventors: SHARMA, Ramnic; H. No. 1012, 2nd Floor, Sector 17B, Gurgaon, Haryana 122015 (IN). ALLU, Senkara, Rao; s/o Bheemu Naidu, Narasimha Puram, Gedda Kancharam, Metta Palli, Srikakulam, Andhra Pradesh 535125 (IN). ARYAN, Ram, Chander; 1066, Sector-A, Pocket-A, Vasant Kunj, New Delhi 110070 (IN). International Publication Number: WO 2013/080069 A1

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Thursday, 11 August 2016

Eran Sella




Eran Sella

Organic Chemist at StoreDot



VEran Sella
Currently: Teva Pharmaceutical Industries
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Technology


Innovative organic compounds

StoreDot technology is based on a unique methodology that has enabled the design, synthesis and tuning of materials to create proprietary organic compounds that dramatically improve the performance of a range of devices, including batteries, displays, sensors and digital memory.

StoreDot’s core technology is based on chemically-synthesized organic molecules of non-biological origin. These innovative molecules demonstrate uniquely tunable optical and electrochemical properties, which allow for the emission of vivid saturated colors, and the enhanced performance of energy storage devices.

Competing technologies are predominantly based on metals, including heavy and toxic metals. By contrast, StoreDot’s organic compounds are non-toxic and environmentally safe. Moreover, they are readily available, manufactured at a fraction of the cost, and therefore superior to any other alternative.


StoreDot Ltd. I 3 Shenkar St. Herzeliya I Israel 4672503  I Phone: +972 3 5097710
Fax: +972 9 7677937 I Email: info@store-dot.com

 Eran Sella Ph.D
Position Title:Ph.D studenteran-2009.jpg
Education:Tel-Aviv University,  B.Sc Chemistry
Contact:eransell@post.tau.ac.il
Tel at Lab:03-6406548

Experience



Organic Chemist

StoreDot
 – Present (less than a year)Israel



Chemical R&D Team Leader

Teva Pharmaceuticals
 –  (1 year)Israel



Research Associate

The Scripps Research Institute
 –  (2 years 2 months)San Diego
Postdoctoral Research in Prof. Phil Baran Lab



Tutorial Assistant

Tel Aviv University
 –  (5 years)
Teaching 'Organic Chemistry II', 'Organic Chemistry for physicians'.



Instructor

Tel Aviv University
 –  (5 years)
Instructor in students' lab 'Organic Chemistry', 'Advanced Organic Chemistry'.

Awards

Excellent Ph.D. Student

Teva Ltd.

Excellent Ph.D. Student

Wolf Foundation Scholarship

Excellent Ph.D. Student

Israel Chemical Society




Publications




Dendritic Chain Reaction(Link)

Journal of the American Chemical Society
July 29, 2009



Two-component Dendritic Chain Reactions: Experiment and Theory(Link)

Journal of the American Chemical Society
March 24, 2010



Sulfhydryl-based Dendritic Chain Reaction(Link)

Chemical Communications
September 21, 2010



A Simple FRET-based Modular Design for Diagnostic Probes(Link)

Organic & Biomolecular Chemistry
November 17, 2011



A Mild, Ferrocene-Catalyzed C-H Imidation of (Hetero)arenes(Link)

Journal of the American Chemical Society
April 2014
Antroquinonol A: Scalable Synthesis and Preclinical Biology of a Phase 2 Drug Candidate

ACS Central Science
December 23, 2015

Education



The Scripps Research Institute

InternshipOrganic Chemistry

Supervisor: Prof. Phil S. Baran




Tel Aviv University

Ph.D., Organic Chemistry





Tel Aviv University

B.Sc, Chemistry
Herzeliya, ISRAEL
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