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3) Provide a detailed mechanism for the illustrated transformation. Use three-dimensional representations where relevant to illustrate the stereochemical aspects of the individual steps. HO (TSOH) H Me H "Et Ме Ме. S. N Ме Et SMe Hint: The sulfonic acid will convert the sulfoxide into a leaving group (see Pummerer reaction) via nucleophilic attack from the indole moiety.

3) Provide a detailed mechanism for the illustrated transformation. Use three-dimensional representations where relevant to illustrate the stereochemical aspects of the individual steps. HO (TSOH) H Me H "Et Ме Ме. S. N Ме Et SMe Hint: The sulfonic acid will convert the sulfoxide into a leaving group (see Pummerer reaction) via nucleophilic attack from the indole moiety.

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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3) Provide a detailed mechanism for the illustrated transformation. Use three-dimensional representations where relevant to illustrate the stereochemical aspects of the individual steps. N- N. Me (TSOH) H ´Et N Ме Ме- S. Ме SMe || Hint: The sulfonic acid will convert the sulfoxide into a leaving group (see Pummerer reaction) via nucleophilic attack from the indole moiety.
Transcribed Image Text:3) Provide a detailed mechanism for the illustrated transformation. Use three-dimensional representations where relevant to illustrate the stereochemical aspects of the individual steps. N- N. Me (TSOH) H ´Et N Ме Ме- S. Ме SMe || Hint: The sulfonic acid will convert the sulfoxide into a leaving group (see Pummerer reaction) via nucleophilic attack from the indole moiety.
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