Volume 19, Issue 4
Isocyclic Compounds
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ChemInform Abstract: Reductive Thiolation of Aromatic Ketones and Benzaldehyde with Sulfur, Carbon Monoxide and Water Leading to Thiols.

Y. NISHIYAMA

Y. NISHIYAMA

Dep. Appl. Chem., Fac. Eng., Kansai Univ., Suita-shi 564, Japan

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Y. OHTORI

Y. OHTORI

Dep. Appl. Chem., Fac. Eng., Kansai Univ., Suita-shi 564, Japan

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S. HAMANAKA

S. HAMANAKA

Dep. Appl. Chem., Fac. Eng., Kansai Univ., Suita-shi 564, Japan

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A. OGAWA

A. OGAWA

Dep. Appl. Chem., Fac. Eng., Kansai Univ., Suita-shi 564, Japan

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S. MURAI

S. MURAI

Dep. Appl. Chem., Fac. Eng., Kansai Univ., Suita-shi 564, Japan

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N. SONODA

N. SONODA

Dep. Appl. Chem., Fac. Eng., Kansai Univ., Suita-shi 564, Japan

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First published: January 26, 1988

Abstract

Reductive sulfurization of the aromatic carbonyl compounds (I) to give the corresponding thiols (II) is achieved by treatment with sulfur, carbon monoxide, and water in the presence of DBU.

ChemInform Abstract

Reductive sulfurization of the aromatic carbonyl compounds (I) to give the corresponding thiols (II) is achieved by treatment with sulfur, carbon monoxide, and water in the presence of DBU. The use of other bases such as Et3N results in lower yields. (Mechanism).

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