Chemoselective N-Acylation of Amines with Acylsilanes under Aqueous Acidic Conditions-Reference-Cited by-同舟云学术

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Chemoselective N-Acylation of Amines with Acylsilanes under Aqueous Acidic Conditions

Published:2023-07-29 Issue:31 Volume:25 Page:5740-5744
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Tian Jing¹²,Li Wei¹,Deng Xingwang¹,Lakshminarayanan Rajamani³,Srinivasan Rajavel¹³^ORCID

Affiliation:

1. School of Pharmaceutical Science and Technology (SPST), Tianjin University, Tianjin 300072, P.R. China

2. Key Laboratory for Tibet Plateau Phytochemistry of Qinghai Province, College of Pharmacy, Qinghai Minzu University, Xining 810007, P. R. China

3. Singapore Eye Research Institute (SERI), The Academia, 20 College Road, Singapore 169856, Singapore

Funder

Tianjin University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c01911

Reference50 articles.

1. Rethinking amide bond synthesis

2. Analysis of the reactions used for the preparation of drug candidate molecules

3. Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?

4. The Most Common Functional Groups in Bioactive Molecules and How Their Popularity Has Evolved over Time

5. Amide bond formation: beyond the myth of coupling reagents

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