Ph3P/ICH2CH2I-promoted reductive deoxygenation of alcohols

Literature Information

Publication Date 2023-11-02
DOI 10.1039/D3OB01698F
Impact Factor 3.876
Authors

Xu Yao, Qu-Tong Zheng, Ji-Chang Xiao


View Original

Abstract

Owing to the ubiquity of the hydroxyl group, reductive deoxygenation of alcohols has become an active research area. The classic Barton–McCombie reaction suffers from a tedious two-step procedure. New efficient methods have been developed, but they have some limitations, such as a narrow substrate scope and the use of moisture-sensitive Lewis acids. In this work, we describe the Ph3P/ICH2CH2I-promoted reductive deoxygenation of alcohols with NaBH4. The process is applicable to benzyl, allyl and propargyl alcohols, and also to primary and secondary alcohols, demonstrating a wide substrate scope and a good level of functional group tolerance. This protocol features convenient operation and low cost of all reagents.

Related Literature

New bi-functional zinc catalysts based on robust and easy-to-handle N-chelating ligands for the synthesis of cyclic carbonates from epoxides and CO2 under mild conditions

Rongchang Luo, Xiantai Zhou, Wuying Zhang, Zhongxiu Liang, Jun Jiang, Hongbing Ji

2014-06-26 Paper

DOI: 10.1039/C4GC00671B

Structural–functional evaluation of ionic liquid libraries for the design of co-solvents in lipase-catalysed reactions

João V. Rodrigues, Diana Ruivo, Ana Rodríguez, Francisco J. Deive, José M. S. S. Esperança, Isabel M. Marrucho, Cláudio M. Gomes, Luís Paulo N. Rebelo

2014-08-04 Communication

DOI: 10.1039/C4GC01329H

Visible-light-induced photocatalytic formyloxylation reactions of 3-bromooxindoles with water and DMF: the scope and mechanism

You-Quan Zou, Wei Guo, Feng-Lei Liu, Liang-Qiu Lu, Jia-Rong Chen

2014-05-08 Paper

DOI: 10.1039/C4GC00647J

Tunable thermomorphism and applications of ionic liquid analogues of Girard's reagents

Marijana Blesic, H. Q. Nimal Gunaratne, Johan Jacquemin, Peter Nockemann, Sonia Olejarz, Kenneth R. Seddon, Christopher R. Strauss

2014-08-06 Communication

DOI: 10.1039/C4GC01159G

Contents list

Front/Back Matter

DOI: 10.1039/C4GC90037E

Fermentation of hydrolysate detoxified by pervaporation through block copolymer membranes

Douglas R. Greer, Thalita P. Basso, Ana B. Ibanez, Stefan Bauer, Jeffrey M. Skerker, A. Evren Ozcam, Dacia Leon, Chaeyoung Shin, Adam P. Arkin

2014-07-11 Paper

DOI: 10.1039/C4GC00756E

Enzymatic synthesis of ionic responsive lignin nanofibres through surface poly(N-isopropylacrylamide) immobilization

Guangzheng Gao, Muzaffer A. Karaaslan, John F. Kadla, Frank Ko

2014-06-23 Paper

DOI: 10.1039/C4GC00757C

Efficient fixation of CO2 into cyclic carbonates catalysed by silicon-based main chain poly-imidazolium salts

Jinquan Wang, Jiayu Leong, Yugen Zhang

2014-07-31 Communication

DOI: 10.1039/C4GC01060D

Flow approaches towards sustainability

Luigi Vaccaro, Daniela Lanari, Assunta Marrocchi, Giacomo Strappaveccia

2014-04-24 Tutorial Review

DOI: 10.1039/C4GC00410H

Electrodeposited CZTS solar cells from Reline electrolyte

Hao Chen, Qinyan Ye, Xulin He, Jingjing Ding, Yongzheng Zhang, Junfeng Han, Jiang Liu, Cheng Liao, Jun Mei, Woonming Lau

2014-05-13 Paper

DOI: 10.1039/C4GC00142G

You might also like

Compound Q&A

How should 2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) be stored?

2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) should be stored in ...

615-45-22-Methylbenzene-1,4-...
Compound Q&A

Is (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide (CAS: 132747-20-7) safe?

(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide is generally considered sa...

132747-20-7(1S,4S)-2,5-Diazabic...
Compound Q&A

What industries use (6-Chloropyridazin-3-YL)methanamine (CAS: 871826-15-2)?

(6-Chloropyridazin-3-YL)methanamine finds applications in the pharmaceutical ind...

871826-15-2(6-Chloropyridazin-3...
Compound Q&A

What are the main uses of 2-Fluoro-3-methylphenol (CAS: 77772-72-6)?

2-Fluoro-3-methylphenol is primarily used in the synthesis of pharmaceuticals, p...

77772-72-62-Fluoro-3-methylphe...
Compound Q&A

What precautions should be taken when handling 3-Methoxy-4-nitrobenzonitrile (CAS: 177476-75-4)?

When handling 3-Methoxy-4-nitrobenzonitrile, it is important to wear appropriate...

177476-75-43-Methoxy-4-nitroben...
Compound Q&A

What precautions should be taken when handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4)?

When handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4), it is ...

211949-57-4[1,3]Oxazolo[4,5-b]p...
Compound Q&A

What regulatory guidelines apply to 4-Ethynylbenzamide (CAS: 90347-86-7)?

4-Ethynylbenzamide (CAS: 90347-86-7) falls under various regulatory guidelines i...

90347-86-74-Ethynylbenzamide
Compound Q&A

What are the main uses of 3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone (CAS: 186822-57-1)?

3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone is primarily used as an intermediat...

186822-57-13-(2-Ethylphenyl)-2-...
Compound Q&A

What is (2-Fluoro-6-methoxyphenyl)acetic acid (CAS: 500912-19-6)?

(2-Fluoro-6-methoxyphenyl)acetic acid, also known as 4-fluoro-3-methoxybenzoic a...

500912-19-6(2-Fluoro-6-methoxyp...
Compound Q&A

What is the market or research trend for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9)?

Market trends for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9) indicat...

102196-18-92-[4-(Hydroxymethyl)...

Source Journal

Organic & Biomolecular Chemistry

Organic & Biomolecular Chemistry
CiteScore: 3.4
Self-citation Rate: 10.3%
Articles per Year: 1041

Organic & Biomolecular Chemistry (OBC) publishes original and high impact research and reviews in organic chemistry. We welcome research that shows new or significantly improved protocols or methodologies in total synthesis, synthetic methodology or physical and theoretical organic chemistry as well as research that shows a significant advance in the organic chemistry or molecular design aspects of chemical biology, catalysis, supramolecular and macromolecular chemistry, theoretical chemistry, mechanism-oriented physical organic chemistry, medicinal chemistry or natural products. Articles published in the journal should report new work which makes a highly-significant impact in the field. Routine and incremental work is generally not suitable for publication in the journal. More details about key areas of our scope are below. In all cases authors should include in their article clear rationale for why their research has been carried out.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.