Universität Wien
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270095 VO Strategies and Tactics in Organic Synthesis (2022S)

3.00 ECTS (2.00 SWS), SPL 27 - Chemie

Registration/Deregistration

Note: The time of your registration within the registration period has no effect on the allocation of places (no first come, first served).

Details

Language: English

Examination dates

Lecturers

Classes (iCal) - next class is marked with N

  • Tuesday 05.04. 16:00 - 18:00 Seminarraum 3 Organische Chemie 1OG Boltzmanngasse 1
  • Thursday 07.04. 10:00 - 12:00 Seminarraum 2 Währinger Straße 38 Dekanat 1. Stock
  • Friday 08.04. 10:00 - 12:00 Seminarraum 2 Währinger Straße 38 Dekanat 1. Stock
  • Tuesday 03.05. 08:15 - 10:15 Hörsaal 4 Chemie HP Währinger Straße 42
  • Wednesday 04.05. 10:00 - 12:00 Seminarraum 3 Organische Chemie 1OG Boltzmanngasse 1
  • Monday 09.05. 15:00 - 17:00 Seminarraum 1 Analytische Chemie 2.OG Boltzmanngasse 1
  • Monday 23.05. 15:00 - 17:00 Seminarraum 2 Währinger Straße 38 Dekanat 1. Stock
  • Wednesday 01.06. 08:15 - 10:15 Kleiner Hörsaal 3 Chemie Boltzmanngasse 1 HP
  • Thursday 09.06. 10:00 - 12:00 Seminarraum 2 Währinger Straße 38 Dekanat 1. Stock

Information

Aims, contents and method of the course

As its name suggests, this lecture aims at discussing how a complex molecule can be approached from a synthetic point of view. In order to do so, selected syntheses will be analysed and commented on. Emphasis shall be placed on retrosynthetic disconnections and their reduction to practice, on maximisation of synthetic efficiency and on the discussion of new methods in Organic Chemistry. Students will be encouraged to think creatively and suggest “out-of-the-box” approaches whenever possible.
For illustrative purposes, an Outline of the main broad topics to be covered and a pool of possible case-studies (typically 1 per lecture) are presented below.

OUTLINE and CASE-STUDY POOL

Sample case-studies

1. Classical approaches to complex molecules
a) Woodward, Strychnine
b) Woodward, Reserpine
c) Corey, Prostaglandins
d) Still, Periplanone B
e) Curran, Hirsutene and Capnellene
f) Corey, Gingkolide

2. Biomimetic approaches
a) Nicolaou, Endiandric Acids
b) Heathcock, Daphnyphillium alkaloids
c) Johnson, Steroids
d) Pirrung, Isocomene
e) Nicolaou, Bisorbicillinoids
f) Shair, Longithorone A
g) Sorensen, FR 182877

3. The past and the future
a) Overman, Strychnine (vs. 1a)
b) Stork, Quinine (vs. Woodward)
c) Volhardt, Steroids (vs. 2c)
d) Grubbs, Capnellene (vs. 1e)
e) Winkler, Manzamine A
f) Corey, Onocerin
g) Baran, Hapalindoles
h) Gin, Batzelladine A

(sample syntheses listed are only illustrative and not all of them will be covered!)

Assessment and permitted materials

Minimum requirements and assessment criteria

Examination topics

Reading list

Classics in Total Synthesis I, Nicolaou et al
Classics in Total Synthesis II, Nicolaou et al
The Logic of Chemical Synthesis, Corey

Association in the course directory

OC-1, EF-1, EF-2, EF-3

Last modified: Tu 13.09.2022 11:29