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Featured researches published by Oliver Krebs.


European Journal of Organic Chemistry | 1999

Allylic Amidation of Olefins by Ene Reaction of Acylnitroso Compounds Generated in situ by Oxidation of Hydroxamic Acids

Waldemar Adam; Nils Bottke; Oliver Krebs; Chantu R. Saha-Möller

A one-pot allylic amidation procedure, which employs the ene reaction of acylnitroso compounds 2 with electron-rich olefins 3a,b, is presented; the acylnitroso enophile is generated in situ by oxidation of hydroxamic acids 1 with iodosobenzene diacetate. The resulting N-allylhydroxamic acids 4 (ene products) are quantitatively acetylated for ease of handling; as an example, the reduction of the acetylated derivative 5b by samarium diiodide was carried out to afford the N-allyl amide 6b in quantitative yields.


European Journal of Organic Chemistry | 2002

A Comparative Study on the Diastereofacial Control in the [4+2] Cycloaddition of Sorbates and the Ene Reaction of Tiglates with Singlet Oxygen and PTAD by a Variety of Chiral Auxiliaries

Waldemar Adam; Sara G. Bosio; Hans-Georg Degen; Oliver Krebs; Dietmar Stalke; Dirk Schumacher

The auxiliary-induced diastereoselectivities of [4+2] cycloaddition and the ene reaction of singlet oxygen and PTAD through a variety of auxiliaries is studied. The different trends in the diastereoselectivities that are observed for the diverse auxiliaries, which include 2,2-dimethyloxazolidines, a menthol derivative, several related cyclohexanes, and the Oppolzer sultam, are compared and backed by mechanistic interpretations. From this overview of two reaction modes for two electrophiles and four different types of auxiliaries, the advantages of the individual auxiliaries become evident and comprehensible. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)


Review of International Economics | 2018

How deep is your love? A quantitative spatial analysis of the transatlantic trade partnership

Oliver Krebs; Michael Pflüger

This paper explores the quantitative consequences of transatlantic trade liberalization envisioned in a Transatlantic Trade and Investment Partnership (TTIP) between the United States and the European Union. Our key innovation is to develop a new quantitative spatial trade model and to use an associated technique which is extraordinarily parsimonious and tightly connects theory and data. We take input-output linkages across industries into account and make use of the recently established World Input Output Database (WIOD). We also explore the consequences of labor mobility across local labor markets in Germany and the countries of the European Union. We address the considerable uncertainties connected both with the quantification of non-tariff trade barriers and the outcome of the negotiations by taking a corridor of trade liberalization paths into account.


Chemical Reviews | 2003

The nitroso ene reaction: A regioselective and stereoselective allylic nitrogen functionalization of mechanistic delight and synthetic potential

Waldemar Adam; Oliver Krebs


Organic Letters | 2005

Synthesis of the Eastern Portion of Ajudazol A Based on Stille Coupling and Double Acetylene Carbocupration

Oliver Krebs; Richard Taylor


Journal of the American Chemical Society | 2002

Efficient π-facial control in the ene reaction of nitrosoarene, triazolinedione, and singlet oxygen with tiglic amides of the bornane-derived sultam as chiral auxiliary: An economical synthesis of enantiomerically pure nitrogen- and oxygen-functionalized acrylic acid derivatives

Waldemar Adam; Hans-Georg Degen; Oliver Krebs; Chantu R. Saha-Möller


Journal of the American Chemical Society | 2000

The Newskewand the EstablishedcisandgemRegioselectivities in the Ene Reaction of Trisubstituted Olefins: Comparison of the Singlet Oxygen, Triazolinedione, and Nitrosoarene Enophiles

Waldemar Adam; Nils Bottke; Oliver Krebs


Journal of Organic Chemistry | 2002

Thionin-Sensitized Intrazeolite Photooxygenation of Trisubstituted Alkenes: Substituent Effects on the Regioselectivity As Probed through Isotopic Labeling

Manolis Stratakis; Radim Nencka; Constantinos Rabalakos; Waldemar Adam; Oliver Krebs


Journal of the American Chemical Society | 2001

An Experimental and Computational Study on the Reactivity and Regioselectivity for the Nitrosoarene Ene Reaction: Comparison with Triazolinedione and Singlet Oxygen

Waldemar Adam; Nils Bottke; and Bernd Engels; Oliver Krebs


Journal of Organic Chemistry | 2003

Intramolecular and intermolecular kinetic isotope effects (KIE) in the nitrosoarene ene reaction: Experimental evidence for reversible intermediate formation

Waldemar Adam; Oliver Krebs; Michael Orfanopoulos; Manolis Stratakis; Georgios C. Vougioukalakis

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Michael Pflüger

German Institute for Economic Research

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Dietmar Stalke

University of Göttingen

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Holger Görg

Kiel Institute for the World Economy

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Georgios C. Vougioukalakis

National and Kapodistrian University of Athens

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