Suppose you are trying to synthesize the dipeptide Val-Ser. Compare the product that would be obtained if

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Suppose you are trying to synthesize the dipeptide Val-Ser. Compare the product that would be obtained if the carboxyl group of N-protected valine were activated with thionyl chloride with the product that would be obtained if the carboxyl group were activated with DCC.

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Organic Chemistry

ISBN: 978-0131407480

4th edition

Authors: Paula Yurkanis Bruice

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