Jürgen Martens

Affiliations: 
1976-1977 Institut für Chemie Carl von Ossietzky Universität Oldenburg 
 1976-1977 Department of Chemistry Harvard University, Cambridge, MA, United States 
 1977-1983 R & D + API Production Degussa Aktiengesellschaft 
 1983-1984 Corporate Planning Degussa Aktiengesellschaft 
 1984-1986 Pharma Division Degussa Aktiengesellschaft 
Area:
Organic chemistry, synthesis, stereochemistry, chromatographyc separation of enantiomers
Website:
https://www.uni-oldenburg.de/oc-martens/
Google:
"Jürgen Martens Oldenburg Chemie"
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Parents

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Klaus Praefcke grad student 1973-1975 TU Berlin
 (Klaus Praefcke was a graduate student with Alexander Schönberg at Technische Universität Berlin)
Robert B. Woodward post-doc 1976-1977 Harvard
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Publications

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Martens J, Bhushan R, Sajewicz M, et al. (2017) Chromatographic Enantioseparations in Achiral Environments: Myth or Truth? J Chromatogr Sci.. 748-749
Nagar H, Martens J, Bhushan R. (2017) Enantioresolution of Three Active Pharmaceutical Ingredients by Different Thin-Layer Chromatographic Approaches J. Planar Chromat.. 30: 350-356
Franz M, Stalling T, Schaper R, et al. (2017) Facile access to amido (thio-)xanthates under eco-friendly conditions by one-pot three-component reaction (3-CR) Synthesis. 49: 4045-4054
Vashistha VK, Martens J, Bhushan R. (2017) Sensitive RP‑HPLC Enantioseparation of (RS)‑Ketamine via Chiral Derivatization Based on (S)‑Levofloxacin Chromatographia. 80: 1501-1508
Ziyaei Halimehjani A, Mohtasham R, Shockravi A, et al. (2016) Multicomponent synthesis of dithiocarbamates starting from vinyl sulfones/sulfoxides and their use in polymerization reactions Rsc Adv.. 6: 75223-75226
Schlüter T, Ziyaei Halimehjani A, Wachtendorf D, et al. (2016) Four-Component Reaction for the Synthesis of Dithiocarbamates Starting from Cyclic Imines. Acs Comb Sci.. 456-460
Martens J, Bhushan R. (2016) Enatioseparations in Achiral Environments and Chromatographic Systems Isr. J. Chem.. 56: 990-1009
Brockmeyer F, Morosow V, Martens J.. (2015) A new multicomponent reaction: unexpected formation of derivatizable cyclic α-alkoxy isothioureas. Org Biomol Chem.. 2441-2444
Kröger D, Schlüter T, Fischer M, et al. (2015) Three-component reaction toward polyannulated quinazolinones, benzoxazinones, and benzothiazinones. Acs Comb Sci.. 202-207
Kröger D, Franz M, Schmidtmann M, et al. (2015) Sequential Multicomponent Reactions and a Cu-Mediated Rearrangement: Diastereoselective Synthesis of Tricyclic Ketones. Org Lett.. 5866-5869
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