English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Our lactamization pro-cess involves the use of triphenylphosphines and water toafford various γ- and δ-lactams in good to excellent yields.Owing to the importance of lactams in natural products andpharmaceuticals, the development of new and diverse routesfor efficient, single-step lactam synthesis from azido amideswith expanded substrate scope is highly desirable. There-fore, we planned to develop another methodology for thedirect lactamization of various azido amides, including 1,5-azido amides to prepare e-lactams. Here, we report a one-potlactamization of 1,3-, 1,4-, and 1,5-azido amides via Bu

One-Pot Synthesis of Five-, Six-, and Seven-Membered Lactams via Bu3SnH-Mediated Reductive Cyclization of Azido Amides

One-Pot Synthesis of Five-, Six-, and Seven-Membered Lactams via Bu₃SnH-Mediated Reductive Cyclization of Azido Amides