Reactions of Aroyl Chlorides with Samarium Metal in DMF—Controllable Syntheses of O‐Aroylbenzoins, 1,2‐Diarylethanones, and (Z)‐α,α′‐Stilbenediol Dibenzoates-Reference-Cited by-同舟云学术

Reactions of Aroyl Chlorides with Samarium Metal in DMF—Controllable Syntheses of O‐Aroylbenzoins, 1,2‐Diarylethanones, and (Z)‐α,α′‐Stilbenediol Dibenzoates

Published:2004-12-31 Issue:21 Volume:34 Page:4009-4022
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Liu Yongjun¹,Wang Xiaoxia²,Zhang Yongmin¹³

Affiliation:

1. a Department of Chemistry , Zhejiang University (Campus Xixi) , Hangzhou, 310028, P. R. China

2. b College of Chemistry and Life Sciences , Zhejiang Normal University , Jinhua, Zhejiang, P. R. China

3. c State Key Laboratory of Organometallic Chemistry , Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , Shanghai, P. R. China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1081/SCC-200034825

Reference49 articles.

1. The coupling of acid chlorides by enneacarbonyldiiron and by nickel carbonyl complexes. Preparation of symmetrical primary alkyl ketones.

2. Titanium-induced reductive coupling reactions. A facile route to tetraphenylfuran

3. An easy coupling of acid chlorides into α-diketones promoted by diiodosamarium

4. Reactions of acyl anions generated from acid chlorides and diiodosamarium

5. Synthesis of .alpha.-ketols mediated by divalent samarium compounds

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