Sulfinimidate Esters as an Electrophilic Sulfinimidoyl Motif Source: Synthesis of N-Protected Sulfilimines from Grignard Reagents-Reference-Cited by-同舟云学术

Sulfinimidate Esters as an Electrophilic Sulfinimidoyl Motif Source: Synthesis of N-Protected Sulfilimines from Grignard Reagents

Published:2021-08-13 Issue:17 Volume:23 Page:6850-6854
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Andresini Michael¹^ORCID,Spennacchio Mauro¹,Colella Marco¹,Losito Gianluca¹,Aramini Andrea²^ORCID,Degennaro Leonardo¹^ORCID,Luisi Renzo¹^ORCID

Affiliation:

1. Flow Chemistry and Microreactor Technology FLAME-Lab, Department of Pharmacy − Drug Sciences, University of Bari “A. Moro”, Via E. Orabona 4, Bari I-70125, Italy

2. Department of Discovery, Dompé Farmaceutici S.p.A., Via Campo di Pile, L’Aquila I-67100, Italy

Funder

Universita degli Studi di Bari Aldo Moro

Ministero dell'Istruzione, dell'UniversitÃ e della Ricerca

DompÃ¨ Farmaceutici spa

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02413

Reference36 articles.

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3. Sulfoximines as Rising Stars in Modern Drug Discovery? Current Status and Perspective on an Emerging Functional Group in Medicinal Chemistry

4. Iron-Catalyzed Amination of Sulfides and Sulfoxides with Azides in Photochemical Continuous Flow Synthesis

5. The Preparation ofN-tert-Butyloxycarbonyl-(Boc-)Protected Sulfoximines and Sulfimines by an Iron(II)-Mediated Nitrene Transfer from BocN3 to Sulfoxides and Sulfides

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