Novel N1−C4 β-Lactam Bond Breakage. Synthesis of Enantiopure α-Alkoxy-γ-keto Acid Derivatives-Reference-Cited by-同舟云学术

Novel N1−C4 β-Lactam Bond Breakage. Synthesis of Enantiopure α-Alkoxy-γ-keto Acid Derivatives

Published:2004-04-22 Issue:11 Volume:6 Page:1765-1767
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Alcaide Benito¹,Almendros Pedro¹,Redondo María C.¹

Affiliation:

1. Departamento de Química Orgánica, Facultad de Química, Universidad Complutense de Madrid, 28040-Madrid, Spain, and Instituto de Química Orgánica General, CSIC, Juan de la Cierva 3, 28006-Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol049549j

Reference13 articles.

1. 4-Oxoazetidine-2-carbaldehydes as useful building blocks in stereocontrolled synthesis

2. Asymmetric synthesis of building-blocks for peptides and peptidomimetics by means of the β-lactam synthon method

3. Two-carbon ring expansion of β-lactams via N(1)C(4) cleavage reactions

4. Synthesis of Optically Pure Highly Functionalized γ-Lactams via 2-Azetidinone-Tethered Iminophosphoranes

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