مورد إلكتروني

Total Syntheses of Xiamycins A, C, F, H and Oridamycin A and Preliminary Evaluation of their Anti-Fungal Properties.

التفاصيل البيبلوغرافية
العنوان: Total Syntheses of Xiamycins A, C, F, H and Oridamycin A and Preliminary Evaluation of their Anti-Fungal Properties.
المؤلفون: Pfaffenbach, Magnus
المصدر: Angewandte Chemie (International ed. in English); vol 58, iss 43, 15304-15308; 1433-7851
بيانات النشر: eScholarship, University of California 2019-10-01
تفاصيل مُضافة: Pfaffenbach, Magnus
Bakanas, Ian
O'Connor, Nicholas R
Herrick, Jessica L
Sarpong, Richmond
نوع الوثيقة: Electronic Resource
مستخلص: Divergent and enantiospecific total syntheses of the indolosesquiterpenoids xiamycins A, C, F, H and oridamycin A have been accomplished. The syntheses, which commence from (R)-carvone, employ a key photoinduced benzannulation sequence to forge the carbazole moiety characteristic of these natural products. Late-stage diversification from a common intermediate enabled the first syntheses of xiamycins C and F, and an unexpected one-pot oxidative decarboxylation, which may prove general, led to xiamycin H. All synthetic intermediates and the natural products were tested for anti-fungal activity. Xiamycin H emerged as an inhibitor of three agriculturally relevant fungal pathogens.
مصطلحات الفهرس: Ustilago, Mitosporic Fungi, Sesquiterpenes, Antifungal Agents, Cyclization, Decarboxylation, Oxidation-Reduction, Stereoisomerism, Light, Cyclohexane Monoterpenes, benzannulation, chiral pool, divergent synthesis, fungitoxicity, total synthesis, Infectious Diseases, Infection, Chemical Sciences, Organic Chemistry, article
URL: https://escholarship.org/uc/item/8b0860s6Test
https://escholarship.orgTest/
الإتاحة: Open access content. Open access content
public
ملاحظة: application/pdf
Angewandte Chemie (International ed. in English) vol 58, iss 43, 15304-15308 1433-7851
أرقام أخرى: CDLER oai:escholarship.org:ark:/13030/qt8b0860s6
qt8b0860s6
https://escholarship.org/uc/item/8b0860s6Test
https://escholarship.orgTest/
1391604090
المصدر المساهم: UC MASS DIGITIZATION
From OAIster®, provided by the OCLC Cooperative.
رقم الانضمام: edsoai.on1391604090
قاعدة البيانات: OAIster