Veit R. Stegmann

432 total citations
11 papers, 337 citations indexed

About

Veit R. Stegmann is a scholar working on Organic Chemistry, Pharmaceutical Science and Inorganic Chemistry. According to data from OpenAlex, Veit R. Stegmann has authored 11 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 4 papers in Pharmaceutical Science and 4 papers in Inorganic Chemistry. Recurrent topics in Veit R. Stegmann's work include Oxidative Organic Chemistry Reactions (9 papers), Radical Photochemical Reactions (6 papers) and Catalytic C–H Functionalization Methods (4 papers). Veit R. Stegmann is often cited by papers focused on Oxidative Organic Chemistry Reactions (9 papers), Radical Photochemical Reactions (6 papers) and Catalytic C–H Functionalization Methods (4 papers). Veit R. Stegmann collaborates with scholars based in Germany. Veit R. Stegmann's co-authors include Waldemar Adam, Chantu R. Saha‐Möller, Rainer T. Fell, Feyissa Gadissa Gelalcha, E.‐M. Peters and Karl Peters and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Synthesis.

In The Last Decade

Veit R. Stegmann

11 papers receiving 321 citations

Peers

Countries citing papers authored by Veit R. Stegmann

Since Specialization

Citations

This map shows the geographic impact of Veit R. Stegmann's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Veit R. Stegmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Veit R. Stegmann more than expected).

Fields of papers citing papers by Veit R. Stegmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Veit R. Stegmann. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Veit R. Stegmann. The network helps show where Veit R. Stegmann may publish in the future.

Co-authorship network of co-authors of Veit R. Stegmann

This figure shows the co-authorship network connecting the top 25 collaborators of Veit R. Stegmann. A scholar is included among the top collaborators of Veit R. Stegmann based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Veit R. Stegmann. Veit R. Stegmann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Unusual Temperature Dependence in the cis/trans-Oxetane Formation Discloses Competitive Syn versus Anti Attack for the Paternò−Büchi Reaction of Triplet-Excited Ketones with cis- and trans-Cylooctenes. Conformational Control of Diastereoselectivity in the Cyclization and Cleavage of Preoxetane Diradicals 2002 ·Journal of the American Chemical Society ·Waldemar Adam, Veit R. Stegmann	27
2	Hydroxy-Group Directivity in the Regioselective and Diastereoselective [2+2] Photocycloaddition (Paternò-Büchi Reaction) of Aromatic Carbonyl Compounds to Chiral and Achiral Allylic Substrates: The Preparation of Oxetanes with up to Three Stereogenic Centers as Synthetic Building Blocks 2002 ·Synthesis ·Waldemar Adam, Veit R. Stegmann	14
3	ChemInform Abstract: Hydroxy‐Group Directivity in the Regioselective and Diastereoselective [2 + 2] Photocycloaddition (Paterno—Buechi Reaction) of Aromatic Carbonyl Compounds to Chiral and Achiral Allylic Substrates: The Preparation of Oxetanes with up to Three Stereogenic Centers as Synthetic Building Blocks. 2001 ·ChemInform ·Waldemar Adam, Veit R. Stegmann	4
4	Unusual Temperature-Dependent Diastereoselectivity in the [2+2] Photocycloaddition (Paternò−Büchi Reaction) of Benzophenone to cis- and trans-Cyclooctene through Conformational Control 2001 ·Journal of the American Chemical Society ·Waldemar Adam, Veit R. Stegmann, (unknown)	15
5	Hydroxy-Directed Regio- and Diastereoselective [2+2] Photocycloaddition (Paternò−Büchi Reaction) of Benzophenone to Chiral Allylic Alcohols 2000 ·Journal of the American Chemical Society ·Waldemar Adam, Karl Peters, E.‐M. Peters, Veit R. Stegmann	54
6	ChemInform Abstract: Chemoselective C—H Oxidation of Alcohols to Carbonyl Compounds with Iodosobenzene Catalyzed by (Salen)chromium Complex. 2000 ·ChemInform ·Waldemar Adam, Feyissa Gadissa Gelalcha, (unknown), Veit R. Stegmann	1
7	Chemoselective C−H Oxidation of Alcohols to Carbonyl Compounds with Iodosobenzene Catalyzed by (Salen)chromium Complex 2000 ·The Journal of Organic Chemistry ·Waldemar Adam, Feyissa Gadissa Gelalcha, Chantu R. Saha‐Möller, Veit R. Stegmann	61
8	ChemInform Abstract: Hydroxy‐Directed Regio‐ and Diastereoselective [2 + 2] Photocycloaddition (Paterno—Buechi Reaction) of Benzophenone to Chiral Allylic Alcohols. 2000 ·ChemInform ·Waldemar Adam, Karl Peters, E.‐M. Peters, Veit R. Stegmann	3
9	Regio- and Diastereoselective Epoxidation of Chiral Allylic Alcohols Catalyzed by Manganese(salen) and Iron(porphyrin) Complexes 1999 ·Journal of the American Chemical Society ·Waldemar Adam, Veit R. Stegmann, Chantu R. Saha‐Möller	39
10	Synthesis of Optically Active α-Hydroxy Carbonyl Compounds by the Catalytic, Enantioselective Oxidation of Silyl Enol Ethers and Ketene Acetals with (Salen)manganese(III) Complexes 1998 ·Journal of the American Chemical Society ·Waldemar Adam, Rainer T. Fell, Veit R. Stegmann, Chantu R. Saha‐Möller	116
11	ChemInform Abstract: Synthesis of Optically Active α‐Hydroxy Carbonyl Compounds by the Catalytic, Enantioselective Oxidation of Silyl Enol Ethers and Ketene Acetals with (Salen)manganese(III) Complexes. 1998 ·ChemInform ·Waldemar Adam, Rainer T. Fell, Veit R. Stegmann, (unknown)	3

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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