Stereoselective synthesis of seven-membered lactams and lactones on a carbohydrate scaffold using ring-closing metathesis-Reference-Cited by-同舟云学术

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Stereoselective synthesis of seven-membered lactams and lactones on a carbohydrate scaffold using ring-closing metathesis

Published:2009-07 Issue:26 Volume:50 Page:3657-3660
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Laventine Dominic L.,Cullis Paul M.,García Marcos D.,Jenkins Paul R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. The use of Carbohydrates in the Synthesis and Configurational Assignments of Optically Active, Non-Carbohydrate Compounds

2. Progeny of 2,3-unsaturated sugars. They little resemble Grandfather Glucose

3. Approaches to the total synthesis of natural products using "chiral templates" derived from carbohydrates

4. Modern Synthetic Methods;Vasella,1980

5. Total Synthesis of Natural Products: The ‘Chiron’ Approach;Hanessian,1983

Cited by 10 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. Metal‐Catalyzed Approaches for the Construction of Azepinones;ChemistrySelect;2022-07-15

2. Design, synthesis and biological evaluation of seco-A-pentacyclic triterpenoids-3,4-lactone as potent non-nucleoside HBV inhibitors;Bioorganic & Medicinal Chemistry Letters;2018-05

3. Olefin Ring‐Closing Metathesis;Organic Reactions;2016-02

4. Synthesis of Lactams by Metathesis Reactions;Topics in Heterocyclic Chemistry;2015

5. Ring-Closing Metathesis;Olefin Metathesis;2014-05-02

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