Academic Journal

A cyclobutanol ring-expansion approach to oxygenated carbazoles: total synthesis of glycoborine, carbazomycin A and carbazomycin B

التفاصيل البيبلوغرافية
العنوان: A cyclobutanol ring-expansion approach to oxygenated carbazoles: total synthesis of glycoborine, carbazomycin A and carbazomycin B
المؤلفون: Natho, P, Allen, LAT, Parsons, PJ
المصدر: 942 ; 937
بيانات النشر: Thieme Gruppe
سنة النشر: 2022
المجموعة: Imperial College London: Spiral
الوصف: The transition-metal-free total syntheses of the oxygenated carbazole natural products glycoborine, carbazomycin A and carbazomycin B are reported. The key step involves an NBS-mediated cyclobutanol ring expansion to 4-tetralones for the preparation of the tricyclic carbazole core.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0936-5214
Relation: Synlett: accounts and rapid communications in synthetic organic chemistry; http://hdl.handle.net/10044/1/103380
DOI: 10.1055/s-0042-1751411
الاتاحة: http://hdl.handle.net/10044/1/103380
https://doi.org/10.1055/s-0042-1751411
Rights: © 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by/4.0/) ; http://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.5ED2D374
قاعدة البيانات: BASE
الوصف
تدمد:09365214
DOI:10.1055/s-0042-1751411