Highly Convergent Three Component Benzyne Coupling: The Total Synthesis of ent-Clavilactone B-Reference-Cited by-同舟云学术

Highly Convergent Three Component Benzyne Coupling: The Total Synthesis of ent-Clavilactone B

Published:2006-10-11 Issue:43 Volume:128 Page:14042-14043
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Larrosa Igor¹,Da Silva Marianne I.¹,Gómez Patricio M.¹,Hannen Peter¹,Ko Eunjung¹,Lenger Steven R.¹,Linke Simon R.¹,White Andrew J. P.¹,Wilton Donna¹,Barrett Anthony G. M.¹

Affiliation:

1. Department of Chemistry, Imperial College London, London SW7 2AZ, England, and AstraZeneca, Process Research and Development, Avlon Works, Severn Road, Hallen, Bristol BS10 7ZE, England

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0662671

Reference20 articles.

1. Secondary mould metabolites. Part 47. Isolation and structure elucidation of clavilactones A–C, new metabolites from the fungus Clitocybe clavipes

2. Structure elucidation of clavilactone D: an inhibitor of protein tyrosine kinases

3. Clavilactones, a novel class of tyrosine kinase inhibitors of fungal origin

4. Receptor Protein-Tyrosine Kinases and Their Signal Transduction Pathways

Cited by 135 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Two Cytochrome P450 Enzymes Form the Tricyclic Nested Skeleton of Meroterpenoids by Sequential Oxidative Reactions;Journal of the American Chemical Society;2024-04-11

2. Synthetic Advantages of Defluorinative C−F Bond Functionalization;Angewandte Chemie;2023-09-14

3. Synthetic Advantages of Defluorinative C−F Bond Functionalization;Angewandte Chemie International Edition;2023-09-14

4. Multicomponent Reactions for the Synthesis of Natural Products and Natural Product-Like Libraries;Drug Discovery and Design Using Natural Products;2023

5. Studies Towards the Total Synthesis of Populusone: Stereoselective Construction of Functionalized 2-Oxa-bicyclo[2.2.2]octenes;Synlett;2022-11-20