Stereoselective synthesis of constrained norbornane-derived spiro-β-lactams-Reference-Cited by-同舟云学术

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Stereoselective synthesis of constrained norbornane-derived spiro-β-lactams

Published:2013-01 Issue:3 Volume:69 Page:1175-1182
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Cremonesi Giuseppe,Dalla Croce Piero,Forni Alessandra,La Rosa Concetta

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference85 articles.

1. For reviews on antibiotic activity of β-lactams, see:

2. The Chemistry of β-Lactams;Page,1992

3. β-Lactams in the New Millennium. Part-II: Cephems, Oxacephems, Penams and Sulbactam

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1. An update on the synthesis and reactivity of spiro-fused β-lactams;Arkivoc;2019-03-30

2. Dynamic Kinetic Resolution of Phosphinic Acid Derivatives via Nucleophilic Substitution at Phosphorus Center;Synthesis;2018-09-05

3. An efficient synthesis of spiro- β-lactams having sulfenyl, sulfinyl and sulfonyl moiety;Journal of Chemical Sciences;2015-11

4. An Easy and Convenient Synthesis of β-Lactams via a One-Pot Staudinger Reaction with 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium Chloride Starting from Substituted Carboxylic Acids;Letters in Organic Chemistry;2015-01-01

5. Special ChiralC2-Symmetricendo-Biarylnorbornane: Synthesis and Structure Illustration;Chinese Journal of Chemistry;2014-07

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