Suppose you are trying to synthesize the dipeptide Val - Ser. Compare the product that would be obtained if thionyl chloride were used to activate the carboxyl group of N - protected valine with the product that would be obtained if it were activated with DCCD. Draw the products which obtained if thionyl chloride is used to activate the carboxyl group of N - protected valine.

Introduction to General, Organic and Biochemistry
11th Edition
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Chapter22: Proteins
Section: Chapter Questions
Problem 22.26P
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Suppose you are trying to
synthesize the dipeptide Val - Ser.
Compare the product that would
be obtained if thionyl chloride
were used to activate the
carboxyl group of N - protected
valine with the product that
would be obtained if it were
activated with DCCD. Draw the
products which obtained if
thionyl chloride is used to
activate the carboxyl group of N
- protected valine.
Transcribed Image Text:Suppose you are trying to synthesize the dipeptide Val - Ser. Compare the product that would be obtained if thionyl chloride were used to activate the carboxyl group of N - protected valine with the product that would be obtained if it were activated with DCCD. Draw the products which obtained if thionyl chloride is used to activate the carboxyl group of N - protected valine.
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