1,4-Diazepinone and Pyrrolodiazepinone Syntheses via Homoallylic Ketones from Cascade Addition of Vinyl Grignard Reagent to α-Aminoacyl-β-amino Esters-Reference-Cited by-同舟云学术

1,4-Diazepinone and Pyrrolodiazepinone Syntheses via Homoallylic Ketones from Cascade Addition of Vinyl Grignard Reagent to α-Aminoacyl-β-amino Esters

Published:2006-07-12 Issue:16 Volume:8 Page:3425-3428
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Iden Hassan S.¹,Lubell William D.¹

Affiliation:

1. Département de chimie, Université de Montréal, C.P. 6128, Succursale Centre Ville, Montréal, Québec, Canada H3C 3J7

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol061036k

Reference31 articles.

1. Design and Synthesis of Novel Scaffolds for Drug Discovery: Hybrids of β-d-Glucose with 1,2,3,4-Tetrahydrobenzo[e][1,4]diazepin-5-one, the Corresponding 1-Oxazepine, and 2- and 4-Pyridyldiazepines

2. Modular Synthesis of Cyclic Peptidomimetics Inspired by γ-Turns

3. 1,4-Diazepane-2,5-diones as novel inhibitors of LFA-1

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