A 11‐Steps Total Synthesis of Magellanine through a Gold(I)‐Catalyzed Dehydro Diels–Alder Reaction

التفاصيل البيبلوغرافية
العنوان: A 11‐Steps Total Synthesis of Magellanine through a Gold(I)‐Catalyzed Dehydro Diels–Alder Reaction
المؤلفون: Louis Barriault, Philippe McGee, Geneviève Bétournay, Francis Barabé
المصدر: Angewandte Chemie International Edition. 56:6280-6283
بيانات النشر: Wiley, 2017.
سنة النشر: 2017
مصطلحات موضوعية: 010405 organic chemistry, Chemistry, Total synthesis, General Medicine, General Chemistry, 010402 general chemistry, 01 natural sciences, Catalysis, Cycloaddition, 0104 chemical sciences, chemistry.chemical_compound, Rapid access, Organic chemistry, Magellanine, Diels–Alder reaction
الوصف: We have developed an innovative strategy for the formation of angular carbocycles via a gold(I)-catalyzed dehydro Diels-Alder reaction. This transformation provides rapid access to a variety of complex angular cores in excellent diastereoselectivities and high yields. The usefulness of this AuI -catalyzed cycloaddition was further demonstrated by accomplishing a 11-steps total synthesis of (±)-magellanine.
تدمد: 1521-3773
1433-7851
DOI: 10.1002/anie.201611606
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad4c86c2b32966f87ade22faba11a960
https://doi.org/10.1002/anie.201611606
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....ad4c86c2b32966f87ade22faba11a960
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15213773
14337851
DOI:10.1002/anie.201611606