1,6-Conjugate addition of <i>in situ</i> generated aryldiazenes to <i>p</i>-quinone methides-Reference-Cited by-同舟云学术

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1,6-Conjugate addition of in situ generated aryldiazenes to p-quinone methides

Published:2024 Issue:27 Volume:22 Page:5636-5645
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Mamale Ajay G.¹²^ORCID,Paul Sayantan¹²,Gonnade Rajesh G.²³^ORCID,Bhattacharya Asish K.¹²^ORCID

Affiliation:

1. Division of Organic Chemistry, CSIR-National Chemical Laboratory (CSIR-NCL), Dr. Homi Bhabha Road, Pune-411 008, India

2. Academy of Scientific and Innovative Research (AcSIR), CSIR-HRDC Campus, Sector 19, Kamla Nehru Nagar, Ghaziabad-201 002, India

3. Central Analytical Facility, CSIR-National Chemical Laboratory (CSIR-NCL), Dr. Homi Bhabha Road, Pune-411 008, India

Abstract

Herein we report a transition-metal free, base-mediated 1,6-conjugate addition of aryldiazenes to para-quinone methides (p-QMs).

Funder

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00618F

Reference37 articles.

1. Recent Advances in the Catalytic Enantioselective Reactions of para -Quinone Methides

2. para -Quinone Methides as Acceptors in 1,6-Nucleophilic Conjugate Addition Reactions for the Synthesis of Structurally Diverse Molecules

3. Recent developments in 1,6-addition reactions of para-quinone methides (p-QMs)

4. Construction of Oxygen‐ and Nitrogen‐based Heterocycles from p ‐Quinone Methides

5. N-Heterocyclic Carbene Catalyzed 1,6-Conjugate Addition of Me3Si-CN to para-Quinone Methides and Fuchsones: Access to α-Arylated Nitriles

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