التفاصيل البيبلوغرافية
| العنوان: |
Access to Chromenopyrrole via Tandem [3 + 2] Cycloaddition and Intramolecular C–O Coupling |
| المؤلفون: |
Bubul Das, Nikita Chakraborty, Hirendra Nath Dhara, Pratip Bhattacharyya, Bhisma K. Patel |
| سنة النشر: |
1753 |
| مصطلحات موضوعية: |
Biophysics, Biochemistry, Medicine, Microbiology, Cell Biology, Genetics, Molecular Biology, Biotechnology, Developmental Biology, Cancer, Infectious Diseases, Virology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, − oh group, intramolecular c –, c5 – h, reaction proceeds via, chromenopyrrole via tandem, 2 ′- hydroxychalcone, situ generated pyrrole, ethyl isocyanoacetate, concise method, bond formation |
| الوصف: |
A mild and concise method for the synthesis of chromenopyrrole from 2′-hydroxychalcone is devised. The reaction proceeds via an initial [3 + 2] cycloaddition on the CC bond of 2′-hydroxychalcone and 1,3-dipolarophile, generated in situ by the reaction of ethyl isocyanoacetate and AgOAc. This is then followed by an intramolecular C–O bond formation with the −OH group and C5–H of the in situ generated pyrrole, leading to chromenopyrroles. |
| نوع الوثيقة: |
article in journal/newspaper |
| اللغة: |
unknown |
| العلاقة: |
https://figshare.com/articles/journal_contribution/Access_to_Chromenopyrrole_via_Tandem_3_2_Cycloaddition_and_Intramolecular_C_O_Coupling/24939054Test |
| DOI: |
10.1021/acs.joc.3c02479.s001 |
| الإتاحة: |
https://doi.org/10.1021/acs.joc.3c02479.s001Test
https://figshare.com/articles/journal_contribution/Access_to_Chromenopyrrole_via_Tandem_3_2_Cycloaddition_and_Intramolecular_C_O_Coupling/24939054Test |
| حقوق: |
CC BY-NC 4.0 |
| رقم الانضمام: |
edsbas.1B37D13A |
| قاعدة البيانات: |
BASE |
