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Florian Mulks (1989-)

Name	Florian Mulks
Time	1989- (Date of birth and death)
Place	Deutschland
Gender	männlich
Academic degree	Dr. rer. nat. (an der Naturwissenschaftlich-Mathematischen Gesamtfakultät der Ruprecht-Karls-Universität Heidelberg) (2018) M.Sc.
Variant	Florian F. Mulks Florian Felix Mulks
Related	Organisch-Chemisches Institut (Heidelberg) (2013-2019) Chemie (Studienfach)
Record type	Person
GND-Identifier	114064971X
Record ID	114064971X
Involved in show all H2-driven biocatalysis for flavin-dependent ene-reduction in a continuous closed-loop flow system utilizing H2 from water electrolysis Diiminium Nucleophile Adducts Are Stable and Convenient Strong Lewis Acids Diiminium Nucleophile Adducts Are Stable and Convenient Strong Lewis Acids ** Diiminium Nucleophile Adducts Are Stable and Convenient Strong Lewis Acids Entropy‐Induced Selectivity Switch in Gold Catalysis: Fast Access to Indolo (1,2‐ a) quinolines Gold carbene complexes and beyond: new avenues in gold(I)-carbon coordination chemistry Gold Catalysis Meets Materials Science – A New Approach to π‐Extended Indolocarbazoles Practical Preparation of Cyclopropenone 1,3-Propanediol Ketal Dibenzothiophenesulfilimines: A Convenient Approach to Intermolecular Rhodium‐Catalysed C−H Amidation Dual Gold/Silver Catalysis Involving Alkynylgold (III) Intermediates Formed by Oxidative Addition and Silver‐Catalyzed C−H Activation for the Direct Alkynylation of Cyclopropenes Gold‐Catalyzed Stereoselective Domino Cyclization/Alkynylation of N ‐Propargylcarboxamides with Benziodoxole Reagents for the Synthesis of Alkynyloxazolines Highly Strained Organogold Complexes and Their Gold‐ or Rhodium‐Catalyzed Isomerizations Cyclopropenylgold (I) Complexes as Aurated Carbenoids or Quasi‐Carbenes On highly strained alkylgold complexes

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Florian Mulks (1989-)

H2-driven biocatalysis for flavin-dependent ene-reduction in a continuous closed-loop flow system utilizing H2 from water electrolysis

Diiminium Nucleophile Adducts Are Stable and Convenient Strong Lewis Acids

Diiminium Nucleophile Adducts Are Stable and Convenient Strong Lewis Acids **

Diiminium Nucleophile Adducts Are Stable and Convenient Strong Lewis Acids

Entropy‐Induced Selectivity Switch in Gold Catalysis: Fast Access to Indolo (1,2‐ a) quinolines

Gold carbene complexes and beyond: new avenues in gold(I)-carbon coordination chemistry

Gold Catalysis Meets Materials Science – A New Approach to π‐Extended Indolocarbazoles

Practical Preparation of Cyclopropenone 1,3-Propanediol Ketal

Dibenzothiophenesulfilimines: A Convenient Approach to Intermolecular Rhodium‐Catalysed C−H Amidation

Dual Gold/Silver Catalysis Involving Alkynylgold (III) Intermediates Formed by Oxidative Addition and Silver‐Catalyzed C−H Activation for the Direct Alkynylation of Cyclopropenes

Gold‐Catalyzed Stereoselective Domino Cyclization/Alkynylation of N ‐Propargylcarboxamides with Benziodoxole Reagents for the Synthesis of Alkynyloxazolines

Highly Strained Organogold Complexes and Their Gold‐ or Rhodium‐Catalyzed Isomerizations

Cyclopropenylgold (I) Complexes as Aurated Carbenoids or Quasi‐Carbenes

On highly strained alkylgold complexes