Microbiological Hydroxylation at Eight Individual Carbon Atoms of Marcfortine A-Reference-Cited by-同舟云学术

Microbiological Hydroxylation at Eight Individual Carbon Atoms of Marcfortine A

Published:1997-11-01 Issue:11 Volume:60 Page:1139-1142
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Lee Byung H.¹,Kornis Gabe I.¹,Cialdella Joyce I.¹,Clothier Michael F.¹,Marshall Vincent P.¹,Martin David G.¹,McNally Patty L.¹,Mizsak Stephen A.¹,Whaley Howard A.¹,Wiley Veronica H.¹

Affiliation:

1. Animal Health Discovery Research, Chemical and Biological Screening, Structural, Analytical and Medicinal Chemistry, Pharmacia and Upjohn Inc., Kalamazoo Michigan 49001

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/np9702805

Reference18 articles.

1. Lynn, R. C.Georgis' Parasitology for Veterinarians;W. B. Saunders Co. Philadelphia, 1995 p 247−294.

2. Anthelmintic resistance

3. Chemical modification of paraherquamide. 2. Replacement of the C-14 methyl group

4. Growth of a Japanese isolate ofTaenia crassiceps in intermediate and definitive hosts

Cited by 9 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. Asymmetric synthesis of chiral 1,2-oxazinane and hexahydropyridazin spirocyclic scaffolds by organocatalytic [4 + 2] cycloaddition;RSC Advances;2022

2. [4 + 3] Cycloaddition of Aromatic α,β-Unsaturated Aldehydes and Ketones with Epoxides: One-Step Approach to Synthesize Seven-Membered Oxacycles Catalyzed by Lewis Acid;The Journal of Organic Chemistry;2010-12-30

3. Chrysogenamide A from an Endophytic Fungus Associated with Cistanche deserticola and Its Neuroprotective Effect on SH-SY5Y Cells;The Journal of Antibiotics;2008-02

4. Synthesis and Modification of Marcfortine and Paraherquamide Class of Anthelmintics;Bioactive Natural Products (Part I);2003

5. Secondary metabolites with antinematodal activity;Bioactive Natural Products;2002