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Nuclear magnetic resonance in structure determination—VII: Stereochemistry of the epoxides of the adducts of cyclopentadiene with α-methyl-β-acetyl acrylic acid lactone

✍ Scribed by Rubén Sánchez-Obregón; Manuel Salmón; Fernando Walls


Publisher
John Wiley and Sons
Year
1972
Tongue
English
Weight
172 KB
Volume
4
Category
Article
ISSN
0749-1581

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✦ Synopsis


By double and triple nuclear magnetic resonance experiments performed at 100 MHz the stereochemistry of the epoxides of Cyclopentadiene with cc-methyl-b-acetyl acrylic acid lactone, were determined to have the exo position. * For part VI, see Ref. 1. t Contribution No.