Home

Uznemiren Laže luk bulis acs aproce kašika registrujte se Univerzalno

Template for Electronic Submission to ACS Journals
Template for Electronic Submission to ACS Journals

Key Aroma Compounds in Lippia dulcis (Dushi Button) | Journal of  Agricultural and Food Chemistry
Key Aroma Compounds in Lippia dulcis (Dushi Button) | Journal of Agricultural and Food Chemistry

Scale-Up and Optimization of a Continuous Flow Carboxylation of  N-Boc-4,4-difluoropiperidine Using s-BuLi in THF,Organic Process Research &  Development - X-MOL
Scale-Up and Optimization of a Continuous Flow Carboxylation of N-Boc-4,4-difluoropiperidine Using s-BuLi in THF,Organic Process Research & Development - X-MOL

PDF) Synthetic Approach to the Core Structure of Oleandrin and Related  Cardiac Glycosides with Highly Functionalized Ring D
PDF) Synthetic Approach to the Core Structure of Oleandrin and Related Cardiac Glycosides with Highly Functionalized Ring D

Nanomaterials | Free Full-Text | Impact of Pretreatment of the Bulk  Starting Material on the Efficiency of Liquid Phase Exfoliation of WS2 |  HTML
Nanomaterials | Free Full-Text | Impact of Pretreatment of the Bulk Starting Material on the Efficiency of Liquid Phase Exfoliation of WS2 | HTML

PDF) Catalytic Asymmetric Synthesis of Diketopiperazines by Intramolecular  Tsuji-Trost Allylation
PDF) Catalytic Asymmetric Synthesis of Diketopiperazines by Intramolecular Tsuji-Trost Allylation

Synthesis of γ-Lactones via the Kowalski Homologation Reaction:  Protecting-Group-Free Divergent Total Syntheses of Eupomatilones-2,5,6, and  3-epi-Eupomatilone-6,Organic Letters - X-MOL
Synthesis of γ-Lactones via the Kowalski Homologation Reaction: Protecting-Group-Free Divergent Total Syntheses of Eupomatilones-2,5,6, and 3-epi-Eupomatilone-6,Organic Letters - X-MOL

Copper-catalyzed radical approach to allenyl iodides - Chemical  Communications (RSC Publishing) DOI:10.1039/C9CC05853B
Copper-catalyzed radical approach to allenyl iodides - Chemical Communications (RSC Publishing) DOI:10.1039/C9CC05853B

Learning From UCLA
Learning From UCLA

PDF) Pot-Economy Autooxidative Condensation of 2-Aryl-2-lithio-1,3-dithianes
PDF) Pot-Economy Autooxidative Condensation of 2-Aryl-2-lithio-1,3-dithianes

Synthesis, Reaction, and Recycle of Fluorous Palladium Catalysts for an  Asymmetric Allylic Alkylation without Using Fluorous Solvents | The Journal  of Organic Chemistry
Synthesis, Reaction, and Recycle of Fluorous Palladium Catalysts for an Asymmetric Allylic Alkylation without Using Fluorous Solvents | The Journal of Organic Chemistry

Synthetic efforts on the road to marine natural products bearing 4- O  -2,3,4,6-tetrasubstituted THPs: an update - RSC Advances (RSC Publishing)  DOI:10.1039/D0RA10755G
Synthetic efforts on the road to marine natural products bearing 4- O -2,3,4,6-tetrasubstituted THPs: an update - RSC Advances (RSC Publishing) DOI:10.1039/D0RA10755G

PDF) Birch Reductive Alkylation of Biaryls: Scope and Limitations
PDF) Birch Reductive Alkylation of Biaryls: Scope and Limitations

Intensification of Continuous Ortho-Lithiation at Ambient  Conditions—Process Understanding and Assessment of Sustainability  Benefits,Organic Process Research & Development - X-MOL
Intensification of Continuous Ortho-Lithiation at Ambient Conditions—Process Understanding and Assessment of Sustainability Benefits,Organic Process Research & Development - X-MOL

Generation and Electrophile Trapping of N -Boc-2-lithio-2-azetine:  Synthesis of 2-Substituted 2-Azetines – topic of research paper in Chemical  sciences. Download scholarly article PDF and read for free on CyberLeninka  open science hub.
Generation and Electrophile Trapping of N -Boc-2-lithio-2-azetine: Synthesis of 2-Substituted 2-Azetines – topic of research paper in Chemical sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub.

PDF) MOP and EE Protecting Groups in Synthesis of α- Or β-Naphthyl-  C-Glycosides from Glycals
PDF) MOP and EE Protecting Groups in Synthesis of α- Or β-Naphthyl- C-Glycosides from Glycals

Synthetic efforts on the road to marine natural products bearing 4- O  -2,3,4,6-tetrasubstituted THPs: an update - RSC Advances (RSC Publishing)  DOI:10.1039/D0RA10755G
Synthetic efforts on the road to marine natural products bearing 4- O -2,3,4,6-tetrasubstituted THPs: an update - RSC Advances (RSC Publishing) DOI:10.1039/D0RA10755G

PM3 optimized structures of [n-BuLi] 4 ·THF 4 and [n-BuLi] 2 ·THF 4.... |  Download Scientific Diagram
PM3 optimized structures of [n-BuLi] 4 ·THF 4 and [n-BuLi] 2 ·THF 4.... | Download Scientific Diagram

Scheme 37. Reaction of n-BuLi with P 4 S 10 | Download Scientific Diagram
Scheme 37. Reaction of n-BuLi with P 4 S 10 | Download Scientific Diagram

Enantioselective Alkylation of 2-Alkylpyridines Controlled by Organolithium  Aggregation.,Journal of the American Chemical Society - X-MOL
Enantioselective Alkylation of 2-Alkylpyridines Controlled by Organolithium Aggregation.,Journal of the American Chemical Society - X-MOL

Green Chemistry
Green Chemistry

Halogen–Lithium Exchange Reaction Using an Integrated Glass Microfluidic  Device: An Optimized Synthetic Approach,Organic Process Research &  Development - X-MOL
Halogen–Lithium Exchange Reaction Using an Integrated Glass Microfluidic Device: An Optimized Synthetic Approach,Organic Process Research & Development - X-MOL

Five-Step Total Synthesis of (±)-Aspidospermidine by a Lactam Strategy via  an Azomethine Ylide | Organic Letters
Five-Step Total Synthesis of (±)-Aspidospermidine by a Lactam Strategy via an Azomethine Ylide | Organic Letters

ACS March 2016 RGC.Final
ACS March 2016 RGC.Final

Synthetic efforts on the road to marine natural products bearing 4- O  -2,3,4,6-tetrasubstituted THPs: an update - RSC Advances (RSC Publishing)  DOI:10.1039/D0RA10755G
Synthetic efforts on the road to marine natural products bearing 4- O -2,3,4,6-tetrasubstituted THPs: an update - RSC Advances (RSC Publishing) DOI:10.1039/D0RA10755G