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Pyrolysis of Sec-Butyl Acetate. Stereospecific Cis Elimination

P. S. Skell / W. L. Hall

The acetates of d,l-threo- and d,l-erythro-3-deuterio-2-butanol were pyrolyzed at 400C. Both cis- and trans-2-butenes were formed in stereospecific cis eliminations. (Author)

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Pyrolysis of Sec-Butyl Acetate. Stereospecific Cis Elimination

P. S. Skell / W. L. Hall

The acetates of d,l-threo- and d,l-erythro-3-deuterio-2-butanol were pyrolyzed at 400C. Both cis- and trans-2-butenes were formed in stereospecific cis eliminations. (Author)

Pyrolysis of Sec-Butyl Acetate. Stereospecific Cis Elimination

P. S. Skell / W. L. Hall

The acetates of d,l-threo- and d,l-erythro-3-deuterio-2-butanol were pyrolyzed at 400C. Both cis- and trans-2-butenes were formed in stereospecific cis eliminations. (Author)

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Title:

Pyrolysis of Sec-Butyl Acetate. Stereospecific Cis Elimination

Contributors:

P. S. Skell (author) / W. L. Hall (author)

Publication date:

1963

Size:

2 pages

Type of media:

Report

Type of material:

No indication

Language:

English

Keywords:

Basic & Synthetic Chemistry , Stereochemistry , Acetates , Pyrolysis , Elimination reactions , Alkenes , Synthesis(Chemistry) , Reprints , Butyl acetates , Butylenes

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