Hydrothiolation of unactivated Alkynes catalyzed by indium(III) bromide
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Yadav, J. S.
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Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, India
Yadav, J. S.
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Reddy, B. V. Subba
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Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, India
Reddy, B. V. Subba
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Raju, A.
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Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, India
Raju, A.
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Ravindar, K.
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Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, India
Ravindar, K.
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Baishya, Gakul
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Baishya, Gakul
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[1] Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, India
Indium(III) bromide is found to catalyze efficiently the hydrothiolation of unactivated alkynes with various thiols under mild conditions to produce the corresponding dithioacetals in excellent yields. However, addition of aromatic thiols on aromatic alkynes gave the beta-vinyl sulfides in high yields. This new procedure offers significant advantages such as high conversions, short reaction times, and simplicity in operation.
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Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, India
Yadav, JS
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Reddy, BVS
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Reddy, BVS
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Krishna, AD
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Krishna, AD
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Swamy, T
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Reddy, BVS
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Bhaishya, G
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Krishna, AD
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Krishna, AD
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Swamy, T
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Reddy, BVS
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Bhaishya, G
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