التفاصيل البيبلوغرافية
العنوان: |
Intramolecular Alkene–Alkene Coupling via Rh(III)-Catalyzed Alkenyl sp 2 C–H Functionalization: Divergent Pathways to Indene or α‑Naphthol Derivatives |
المؤلفون: |
Manikantha Maraswami (4335442), Thomas Diggins (11371087), Jeffrey Goh (9712776), Raymond Tio (11371090), Wan Qing Renee Ong (11371093), Hajime Hirao (1269615), Teck-Peng Loh (1433638) |
سنة النشر: |
2021 |
المجموعة: |
Smithsonian Institution: Digital Repository |
مصطلحات موضوعية: |
Biochemistry, Medicine, Microbiology, Genetics, Molecular Biology, Neuroscience, Physiology, Biotechnology, Evolutionary Biology, Immunology, Cancer, Infectious Diseases, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, different alkene pairs, reaction also allow, 2 sup, alkene functionalities, reaction works, reaction pathway, satisfactory yields, naphthol derivatives, divergent pathways, corresponding products |
الوصف: |
Highly selective synthesis of either indene or 1-naphthol derivatives through intramolecular alkene–alkene cross-coupling is reported. The reaction works with different alkene pairs that couple to give the corresponding products in good to satisfactory yields. The indene products of our reaction also allow further derivatization. The reaction pathway is dependent on alkene functionalities. |
نوع الوثيقة: |
article in journal/newspaper |
اللغة: |
unknown |
العلاقة: |
https://figshare.com/articles/journal_contribution/Intramolecular_Alkene_Alkene_Coupling_via_Rh_III_-Catalyzed_Alkenyl_sp_sup_2_sup_C_H_Functionalization_Divergent_Pathways_to_Indene_or_Naphthol_Derivatives/16553329Test |
DOI: |
10.1021/acscatal.1c03175.s001 |
الإتاحة: |
https://doi.org/10.1021/acscatal.1c03175.s001Test |
حقوق: |
CC BY-NC 4.0 |
رقم الانضمام: |
edsbas.CF4622E |
قاعدة البيانات: |
BASE |