Literature DB >> 17294412

The Woodward-Doering/Rabe-Kindler total synthesis of quinine: setting the record straight.

Jeffrey I Seeman1.   

Abstract

In 1918, Paul Rabe and Karl Kindler reported the three-step conversion of d-quinotoxine into quinine. In 1944 Robert B. Woodward and William von Eggers Doering reported the total synthesis of homomeroquinene and d-quinotoxine from 7-hydroxyisoquinoline. Based on the transformations by Rabe and Kindler, Woodward and Doering asserted the "Total Synthesis of Quinine" (the title of their 1944 and 1945 papers). In 2000 and 2001, Gilbert Stork concluded that the claim by Woodward and Doering is a "myth" because they had synthesized only homomeroquinene and d-quinotoxine; no synthetic quinine had been made in Cambridge. In fact, Rabe and Kindler never published the experimental details of their conversion of d-quinotoxine into quinine. This Review presents the results of a detailed examination of the synthesis of cinchona alkaloids, and previously unpublished material combined with unpublished material and numerous interviews give insight into the lives of the personalities in this nearly 100-year saga.

Entities:  

Year:  2007        PMID: 17294412     DOI: 10.1002/anie.200601551

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  9 in total

Review 1.  Bright ideas for chemical biology.

Authors:  Luke D Lavis; Ronald T Raines
Journal:  ACS Chem Biol       Date:  2008-03-20       Impact factor: 5.100

2.  Rabe rest in peace: confirmation of the rabe-kindler conversion of D-quinotoxine into quinine: experimental affirmation of the Woodward-Doering formal total synthesis of quinine.

Authors:  Aaron C Smith; Robert M Williams
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

3.  Intermolecular radical addition to N-acylhydrazones as a stereocontrol strategy for alkaloid synthesis: formal synthesis of quinine.

Authors:  Gregory K Friestad; An Ji; Chandra Sekhar Korapala; Jun Qin
Journal:  Org Biomol Chem       Date:  2011-05-03       Impact factor: 3.876

4.  "For Its Size, the Most Complex Natural Product Known." Who Deserves Credit for Determining the Structure of Strychnine?

Authors:  Jeffrey I Seeman; Mark C House
Journal:  ACS Cent Sci       Date:  2022-06-08       Impact factor: 18.728

5.  Concise stereocontrolled formal synthesis of (+/-)-quinine and total synthesis of (+/-)-7- hydroxyquinine via merged Morita-Baylis-Hillman-Tsuji-Trost cyclization.

Authors:  Peter Webber; Michael J Krische
Journal:  J Org Chem       Date:  2008-12-05       Impact factor: 4.354

6.  Organic Synthesis: Wherefrom and Whither? (Some Very Personal Reflections).

Authors:  Scott E Denmark
Journal:  Isr J Chem       Date:  2017-10-23       Impact factor: 3.333

Review 7.  Natural Products That Changed Society.

Authors:  Søren Brøgger Christensen
Journal:  Biomedicines       Date:  2021-04-26

8.  Preface. Ethics and Responsible Conduct of Research within the Chemical Community. Ideas and Experiences Worth Sharing.

Authors:  Jeffrey I Seeman
Journal:  Account Res       Date:  2015       Impact factor: 2.622

9.  C-H Activation Enables a Concise Total Synthesis of Quinine and Analogues with Enhanced Antimalarial Activity.

Authors:  Daniel H O' Donovan; Paul Aillard; Martin Berger; Aurélien de la Torre; Desislava Petkova; Christian Knittl-Frank; Danny Geerdink; Marcel Kaiser; Nuno Maulide
Journal:  Angew Chem Int Ed Engl       Date:  2018-06-22       Impact factor: 16.823

  9 in total

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