• Find an Expert
  • Search iconSearch
  • Menu
  • Help
  • Report an issue

Contact


Email

shorvat@unimelb.edu.au

Credentials


Position
1st Year Co-Ordinator And Lecturer
Chemistry
Education
Doctor of Philosophy
University of Melbourne

Dr. Sonia Horvat

1st Year Co-Ordinator And Lecturer
Chemistry

14 Scholarly works
0 Projects

HIGHLIGHTS

  • 2014

    Journal article

    An ab initio and DFT study of some homolytic substitution reactions of methoxycarbonyl radicals at silicon, germanium, and tin
    DOI: 10.1039/c3nj01394d
  • 2013

    Journal article

    Deconvoluting the Reactivity of Two Intermediates Formed from Modified Pyrimidines
    DOI: 10.1021/ol401472m
  • 2013

    Journal article

    Rate Coefficients for Intramolecular Homolytic Substitution of Oxyacyl Radicals at Sulfur
    DOI: 10.1071/CH12477
  • 2012

    Journal article

    An ab initio and DFT study of homolytic substitution reactions by oxyacyl radicals at sulfur, selenium, and tellurium
    DOI: 10.1016/j.tet.2012.06.098
  • 2012

    Conference Proceedings

    Homolytic substitution chemistry: From James Franz to antihypertensives
    DOI: 10.1002/chin.201230258
  • 2012

    Conference Proceedings

    Rate coefficients for intramolecular homolytic substitution of oxyacyl radicals at selenium
    DOI: 10.1002/kin.20604
  • 2010

    Journal article

    An ab initio and DFT study of homolytic substitution reactions of acyl radicals at sulfur, selenium, and tellurium
    DOI: 10.1039/c0nj00125b
Sonia Horvat

RECENT SCHOLARLY WORKS

  • 2009

    Journal article

    Ab Initio and DFT Study of Homolytic Substitution Reactions of Acyl Radicals at Silicon, Germanium, and Tin
    DOI: 10.1021/om801016x
  • 2003

    Journal article

    Homolytic 1,5-transfer of chiral organosilicon groups from an enoxy oxygen to an alkoxy oxygen - implications for mechanism
    DOI: 10.1039/b302307a
  • 2003

    Journal article

    Methyl radical also reacts by the frontside mechanism: An ab initio study of some homolytic substitution reactions of methyl radical at silicon, germanium and tin
    DOI: 10.1039/b211310d
  • 2002

    Journal article

    Understanding homolytic translocation chemistry - An ab initio study of some 1,5-transfers of silyl, germyl and stannyl groups of synthetic significance
    DOI: 10.1071/CH02147
  • 2001

    Journal article

    Polysilane and related radical rearrangements: an ab initio study of (1,2)-silyl, germyl and stannyl translocations in radicals derived from trisilanes and related species
    DOI: 10.1039/b100162k
  • 2000

    Journal article

    Free Radical Homolytic Substitution by the Frontside Mechanism: Ab Initio Study of Homolytic Substitution Reactions at Silicon, Germanium, and Tin
    DOI: 10.1021/om990886j
  • 1998

    Journal article

    Reactions of beta-trimethylstannylcyclohexanones with peracids: investigations into the stannyl-directed Baeyer-Villiger reaction
    DOI: 10.1039/a804427i

UNIVERSITY SEARCH

›  

Current students

›  

Staff

›  

Alumni

  

Faculties & graduate schools

  

Library

  

Contact us

  

Maps

  

Support the campaign

  

Jobs

facebookIcontwitterIconlinkedinIcon


Phone: 13 MELB ( 13 6352)

International: +61 3 9035 5511

ABN: 84 002 705 224

CRICOS Provider Code:
00116K ( visa information)

Emergency information  |  Disclaimer and copyright  |  Accessibility  |  Privacy

STUDY AT MELBOURNE

›  Find a course

›  Admissions, fees & applications

›  International students

›  Campus tour

›  Connect with us

›  Accommodation

ABOUT US

›  Strategy and leadership

›  Tradition of excellence

›  International connections

›  Campuses and facilities

›  Structure and governance

›  Policy and publications

›  Careers at Melbourne

›  Supplying to the University

CONTACT & MAPS

›  Enquiries

›  Media

›  Find an expert

›  Campus maps

›  Traffic, parking & bicycles

›  Find a staff member

ALUMNI & FRIENDS

›  Benefits & services

›  Give

›  Volunteer

›  3010: alumni magazine

RESEARCH

›  Research institute

›  Find an expert or supervisor

›  Graduate researchers

›  Pursuit: our research showcase

ENGAGEMENT

›  Events

›  Sports facilities

›  Shop

We acknowledge and pay respect to the Traditional Owners of the lands upon which our campuses are situated.