A Dipolar Cycloaddition Strategy for the Synthesis of 3,8-Diazabicyclo[3.2.1]Octane Tetrahydroisoquinoline Antitumor Antibiotics: The Total Synthesis of (−)-Lemonomycin-Reference-Cited by-同舟云学术

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A Dipolar Cycloaddition Strategy for the Synthesis of 3,8-Diazabicyclo[3.2.1]Octane Tetrahydroisoquinoline Antitumor Antibiotics: The Total Synthesis of (−)-Lemonomycin

Published:2012 Issue: Volume: Page:351-373
ISSN:1874-6004
Container-title:Strategies and Tactics in Organic Synthesis Volume 8
language:
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Author:

Ashley Eric,Stoltz Brian

Publisher

Elsevier

Reference60 articles.

1. Chemistry and Biology of the Tetrahydroisoquinoline Antitumor Antibiotics

2. Structural elucidation of lemonomycin, a potent antibiotic from Streptomyces candidus

3. Glycothiohexides, novel antibiotics produced by "Sebekia" sp. I.-14E605. L Taxonomy, fermentation and biological evaluation.

4. Glycothiohexide .ALPHA., a novel antibiotic produced by "Sebekia" sp., LL-14E605. II. Isolation and physical-chemical characterization.

Cited by 4 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. Potent Antibiotic Lemonomycin: A Glimpse of Its Discovery, Origin, and Chemical Synthesis;Molecules;2022-07-05

2. Development of the Vinylogous Pictet–Spengler Cyclization and Total Synthesis of (±)‐Lundurine A;Angewandte Chemie International Edition;2018-05-04

3. Development of the Vinylogous Pictet–Spengler Cyclization and Total Synthesis of (±)‐Lundurine A;Angewandte Chemie;2018-05-04

4. ChemInform Abstract: A Dipolar Cycloaddition Strategy for the Synthesis of 3,8-Diazabicyclo[3.2.1]octane Tetrahydroisoquinoline Antitumor Antibiotics. The Total Synthesis of (-)-Lemonomycin;ChemInform;2013-07-11

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