A Pd-catalyzed one-pot cascade consisting of C–C/C–O/N–N bond formation to access benzoxazine fused 1,2,3-triazoles-Reference-Cited by-同舟云学术

A Pd-catalyzed one-pot cascade consisting of C–C/C–O/N–N bond formation to access benzoxazine fused 1,2,3-triazoles

Published:2021 Issue:45 Volume:19 Page:9936-9945
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Soam Pooja¹,Gaba Hashmita¹,Mandal Debasish¹,Tyagi Vikas¹^ORCID

Affiliation:

1. School of Chemistry and Biochemistry, Thapar Institute of Engineering and Technology, Patiala-147004, Punjab, India

Abstract

A Pd-catalyzed one-pot cascade consisting of C–C/C–O/N–N bond formation to access clinically important fused 1,2,3-triazoles using N-aryl-α-(tosylhydrazone)acetamides with isocyanide has been developed.

Funder

Department of Science and Technology, Ministry of Science and Technology, India

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01539G

Reference54 articles.

1. Di- and Trisubstituted γ-Lactams via Rh(II)-carbenoid Reaction of N-Cα-Branched, N-Bis(trimethylsilyl)methyl α-Diazoamides. Synthesis of (±)-α-Allokainic Acid

2. Palladium Catalysis in the Intramolecular Carbene C-H Insertion of α-Diazo-α-(methoxycarbonyl)acetamides to Form β-Lactams

3. Thermally induced reaction of diazoamides with isatins: A complementary approach to the 3,3′-bioxindole derivatives

4. Chemo‐selective Rh(II)/Pd(0) Dual Catalysis: Synthesis of All‐Carbon C3‐Quaternary Allylic Oxindoles from N ‐Aryl‐ α ‐Diazo‐ β ‐Keto‐Amides with Functionalized Allyl Carbonates

5. Substrate and catalyst effects in C–H insertion reactions of α-diazoacetamides

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