A formal synthesis of (-)-pumiliotoxin C

An asymmetric synthesis of an advanced intermediate in the synthesis of natural (-)-pumiliotoxin C has been achieved in six steps and in 61% overall yield employing as the key step a highly diastereoselective lithium amide 1,4-conjugate addition to a dienoic ester derived from (R)-(+)-pulegone.

Bibliographic Details
Main Authors: Davies, S, Bhalay, G
Format: Journal article
Published: 1996
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author Davies, S
Bhalay, G
author_facet Davies, S
Bhalay, G
author_sort Davies, S
collection OXFORD
description An asymmetric synthesis of an advanced intermediate in the synthesis of natural (-)-pumiliotoxin C has been achieved in six steps and in 61% overall yield employing as the key step a highly diastereoselective lithium amide 1,4-conjugate addition to a dienoic ester derived from (R)-(+)-pulegone.
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spelling oxford-uuid:aee971e0-0318-49a1-8562-9098148c53a82022-03-27T03:45:59ZA formal synthesis of (-)-pumiliotoxin CJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:aee971e0-0318-49a1-8562-9098148c53a8Symplectic Elements at Oxford1996Davies, SBhalay, GAn asymmetric synthesis of an advanced intermediate in the synthesis of natural (-)-pumiliotoxin C has been achieved in six steps and in 61% overall yield employing as the key step a highly diastereoselective lithium amide 1,4-conjugate addition to a dienoic ester derived from (R)-(+)-pulegone.
spellingShingle Davies, S
Bhalay, G
A formal synthesis of (-)-pumiliotoxin C
title A formal synthesis of (-)-pumiliotoxin C
title_full A formal synthesis of (-)-pumiliotoxin C
title_fullStr A formal synthesis of (-)-pumiliotoxin C
title_full_unstemmed A formal synthesis of (-)-pumiliotoxin C
title_short A formal synthesis of (-)-pumiliotoxin C
title_sort formal synthesis of pumiliotoxin c
work_keys_str_mv AT daviess aformalsynthesisofpumiliotoxinc
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