The effect of propargylic substitution on the activation and aromatization of enediynes-Reference-Cited by-同舟云学术

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The effect of propargylic substitution on the activation and aromatization of enediynes

Published:1994-12-22 Issue:24 Volume:4 Page:2925-2928
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Wittman Mark D.,Kadow John F.,Pham Kahnie,Kinwa Leung,Mastalerz Harold A.,Vyas Dolatrai M.,Rose William C.,Solomon Wyle,Zein Nada

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference12 articles.

1. Esperamicins, a novel class of potent antitumor antibiotics. 3. Structures of esperamicins A1, A2, and A1b

2. Calichemicins, a novel family of antitumor antibiotics. 1. Chemistry and partial structure of calichemicin .gamma.1I

3. Crystal and molecular structure of dynemicin A: a novel 1,5-diyn-3-ene antitumor antibiotic

4. Protein damage caused by a synthetic enediyne core

5. Conjugate addition-aldol approach to the simple bicyclic-diynene core structure found in the esperamicins and calicheamicins

Cited by 2 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. Effects of Propargylic Substitution and Annelation on the Cycloaromatization of a Bicyclo[7.3.1] Enediyne;The Journal of Organic Chemistry;1999-05-14

2. Synthesis of an esperamicin core analog with an epoxide trigger;Tetrahedron Letters;1996-11

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