Regioselective Quinazolinone-Directed Ortho Lithiation of Quinazolinoylquinoline: Practical Synthesis of Naturally Occurring Human DNA Topoisomerase I Poison Luotonin A and Luotonins B and E-Reference-Cited by-同舟云学术

Regioselective Quinazolinone-Directed Ortho Lithiation of Quinazolinoylquinoline: Practical Synthesis of Naturally Occurring Human DNA Topoisomerase I Poison Luotonin A and Luotonins B and E

Published:2004-06-01 Issue:13 Volume:69 Page:4563-4566
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Mhaske Santosh B.¹,Argade Narshinha P.¹

Affiliation:

1. Combi Chem-Bio Resource Center, Division of Organic Chemistry (Synthesis), National Chemical Laboratory, Pune 411 008, India %argade@dalton.ncl.res.in

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo040153v

Reference52 articles.

1. Advances in the directed metallation of azines and diazines (pyridines, pyrimidines, pyrazines, pyridazines, quinolines, benzodiazines and carbolines). Part 1: Metallation of pyridines, quinolines and carbolines

2. Synthesis of Substituted Quinazolin-4(3H)-ones and Quinazolines via Directed Lithiation

3. Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics

4. Metalation and electrophilic substitution of amine derivatives adjacent to nitrogen: .alpha.-metallo amine synthetic equivalents

5. The Carboxylic Acid Group as an Effective Director of Ortho-Lithiation

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