Transition-metal and base-free ether synthesis via alcohol-participated yne-allylic substitution DOI Creative Commons
Chao Xu,

Yingkun Luo,

Shengtong Niu

и другие.

Green Synthesis and Catalysis, Год журнала: 2023, Номер unknown

Опубликована: Окт. 1, 2023

Ethers are among the most important chemicals in organic synthesis, pharmaceutical industry, agrochemical production, and material science. C-O bond formation via substitution is one of widely used strategies for ether formation. However, known methods usually employ transition-metal bases to facilitate process. In this work, we describe base- transition-metal-free alcohol phenol-participated substitution. The protocol allows access a large number ethers with enyne functional moieties, features mild reaction conditions, high efficiency, good regio- stereoselectivities. could be readily scaled up, products range further transformations.

Язык: Английский

Recent advances in the synthesis and reactivity of MIDA boronates DOI

Debasis Aich,

Parveen Kumar,

Debraj Ghorai

и другие.

Chemical Communications, Год журнала: 2022, Номер 58(96), С. 13298 - 13316

Опубликована: Янв. 1, 2022

MIDA boronates have been widely applied as building blocks in the synthesis of natural products and pharmaceuticals precursors. This review highlights recent advances provides a comprehensive summary their reactivity.

Язык: Английский

Процитировано

16

Transition‐Metal‐Free Heterocyclic Carbon‐Boron Bond Formation DOI

Subrata Hazra,

Somenath Mahato,

Kanak Kanti Das

и другие.

Chemistry - A European Journal, Год журнала: 2022, Номер 28(44)

Опубликована: Апрель 19, 2022

Abstract Heteroaryl boronic acids and esters are extremely important valuable intermediates because of their wide application in the synthesis marketed drugs bioactive compounds. Over last couple decades, construction highly heteroaryl carbon‐boron bonds has created huge attention. The transition‐metal‐free protocols more green, less sensitive to air moisture, also economically advantageous over transition‐metal‐based protocols. C−H borylation heteroarenes C−X (X=halogen) halides represents an excellent approach for synthesis. Also, various cyclization alkyne activation have been recently established goal this review article is summarize existing literature current state art acid esters.

Язык: Английский

Процитировано

15

Base‐Mediated Radical Borylation of Alkyl Sulfones DOI
Mingming Huang, Jiefeng Hu, Ivo Krummenacher

и другие.

Chemistry - A European Journal, Год журнала: 2021, Номер 28(3)

Опубликована: Окт. 29, 2021

A practical and direct method was developed for the production of versatile alkyl boronate esters via transition metal-free borylation primary secondary sulfones. The key to success strategy is use bis(neopentyl glycolato) diboron (B

Язык: Английский

Процитировано

20

Aluminium‐Catalyzed Selective Hydroboration of Esters and Epoxides to Alcohols: C−O Bond Activation DOI
Nabin Sarkar, Rajata Kumar Sahoo, Sharanappa Nembenna

и другие.

Chemistry - A European Journal, Год журнала: 2022, Номер 29(4)

Опубликована: Окт. 13, 2022

In this work, the molecular aluminium dihydride complex bearing an N, N'-chelated conjugated bis-guanidinate (CBG) ligand is used as a catalyst for reducing wide range of aryl and alkyl esters with good tolerance alkene (C=C), alkyne (C≡C), halides (Cl, Br, I F), nitrile (C≡N), nitro (NO2 ) functionalities. Further, we investigated catalytic application in C-O bond cleavage epoxides into corresponding branched Markovnikov ring-opening products. addition, chemoselective intermolecular reduction over other reducible functional groups, such amides alkenes, has been established. Intermediates are isolated characterized by NMR HRMS studies, which confirm probable cycles hydroboration epoxides.

Язык: Английский

Процитировано

13

Transition-metal and base-free ether synthesis via alcohol-participated yne-allylic substitution DOI Creative Commons
Chao Xu,

Yingkun Luo,

Shengtong Niu

и другие.

Green Synthesis and Catalysis, Год журнала: 2023, Номер unknown

Опубликована: Окт. 1, 2023

Ethers are among the most important chemicals in organic synthesis, pharmaceutical industry, agrochemical production, and material science. C-O bond formation via substitution is one of widely used strategies for ether formation. However, known methods usually employ transition-metal bases to facilitate process. In this work, we describe base- transition-metal-free alcohol phenol-participated substitution. The protocol allows access a large number ethers with enyne functional moieties, features mild reaction conditions, high efficiency, good regio- stereoselectivities. could be readily scaled up, products range further transformations.

Язык: Английский

Процитировано

6