✦ LIBER ✦

Reductive bromination of aromatic aldehydes using alkylboron dibromides

✍ Scribed by George W Kabalka; Zhongzhi Wu; Yuhong Ju

Book ID: 104210494
Publisher: Elsevier Science
Year: 2000
Tongue: French
Weight: 146 KB
Volume: 41
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)00811-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Reductive Brominati

ChemInform Abstract: Reductive Bromination of Aromatic Aldehydes Using Alkylboron Dibromides.

✍ George W. Kabalka; Zhongzhi Wu; Yuhong Ju 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Alkylation of aromatic aldehydes with al

Alkylation of aromatic aldehydes with alkylboron chloride derivatives

✍ George W Kabalka; Zhongzhi Wu; Yuhong Ju 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 126 KB

Reductive Amination of Aromatic Aldehyde

Reductive Amination of Aromatic Aldehydes Using NADH Models

✍ Serjinder Singh; Vijay K. Sharma 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 131 KB

ChemInform Abstract: Alkylation of Aroma

ChemInform Abstract: Alkylation of Aromatic Aldehydes with Alkylboron Chloride Derivatives.

✍ George W. Kabalka; Zhongzhi Wu; Yuhong Ju 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

Reductive etherification of aromatic ald

Reductive etherification of aromatic aldehydes with decaborane

✍ Seung Hwan Lee; Yong June Park; Cheol Min Yoon 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 98 KB

Chloroalkylation of aryl aldehydes using

Chloroalkylation of aryl aldehydes using alkylboron dichlorides in the presence of oxygen

✍ George W Kabalka; Zhongzhi Wu; Yuhong Ju 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 63 KB

Reactions of aryl aldehydes with alkylboron dichlorides in the presence of oxygen at room temperature produces arylalkyl chlorides in good to excellent yields.