Alexandria Digital Research Library

The Synthesis of (+)-Brevisamide, (+)-NPS R-568 and Cinacalcet

Author:
Martinez, Steven Ronnie
Degree Grantor:
University of California, Santa Barbara. Chemistry
Degree Supervisor:
Armen Zakarian
Place of Publication:
[Santa Barbara, Calif.]
Publisher:
University of California, Santa Barbara
Creation Date:
2013
Issued Date:
2013
Topics:
Chemistry, Organic
Keywords:
Achmatowicz Rearrangement
Enantioselective alkylation via a chiral amine base
Total synthesis
Koga base
Asymmetric Henry Reaction
Protecting group-free
Genres:
Online resources and Dissertations, Academic
Dissertation:
M.S.--University of California, Santa Barbara, 2013
Description:

Protecting groups play an important role in the process of multistep synthesis of complex molecules due to functional group tolerance. Specific functional groups cannot survive required reagents or chemical environments in the process to synthesis a target molecule so they must be protected to survive the reaction conditions and later be deprotect to their original form. However, protecting a functional group is not ideal because it adds additional steps and material costs to the process. To enhance the efficiency of the synthesis of (+)-Brevisamide, (+)-NPS R-568 and Cinacalcet we kept in mind the concept of being atom economical by avoiding protecting groups.

Physical Description:
1 online resource (95 pages)
Format:
Text
Collection(s):
UCSB electronic theses and dissertations
ARK:
ark:/48907/f3k64g2b
ISBN:
9781303426254
Catalog System Number:
990040770660203776
Rights:
Inc.icon only.dark In Copyright
Copyright Holder:
Steven Martinez
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