April 29, 2024, 08:39:53 PM
Forum Rules: Read This Before Posting


Topic: Retron?  (Read 9041 times)

0 Members and 1 Guest are viewing this topic.

Offline narin

  • New Member
  • **
  • Posts: 6
  • Mole Snacks: +0/-0
Retron?
« on: January 13, 2012, 01:52:03 PM »
could someone elaborate on what a retron is in terms of retrosynthesis and how it differs from a synthon?

Offline discodermolide

  • Chemist
  • Sr. Member
  • *
  • Posts: 5038
  • Mole Snacks: +405/-70
  • Gender: Male
    • My research history
Re: Retron?
« Reply #1 on: January 13, 2012, 05:16:55 PM »
could someone elaborate on what a retron is in terms of retrosynthesis and how it differs from a synthon?

A retron would be an intermediate on the retro synthetic pathway. A synthon is a compound utilized in the synthetic pathway.
Development Chemists do it on Scale, Research Chemists just do it!
My Research History

Offline OrgoTutor

  • Regular Member
  • ***
  • Posts: 13
  • Mole Snacks: +5/-0
  • Gender: Male
  • Freelance Organic Chemistry Tutor
Re: Retron?
« Reply #2 on: January 17, 2012, 12:59:22 AM »
could someone elaborate on what a retron is in terms of retrosynthesis and how it differs from a synthon?

I'm not sure how standardized the terms "retron" and "synthon" are in industry or academia, but here's how I understand them:

"Retron," coined by E J Corey, can be used to refer to a particular portion of a molecule which indicates what retrosynthetic "transform" (the opposite of a forward-direction synthetic reaction) can be used to reduce structural complexity. So for example, ethyl acetoacetate exhibits the retron (ie, the 1,3-dicarbonyl) for a Claisen condensation transform.

"Synthon" is used in the "disconnection method" of retrosynthesis (cf. Stuart Warren's book), and it refers to the imaginary fragments that result from breaking a bond heterolytically. The synthons which result from disconnecting ethyl acetoacetate at the bond between carbon 2 and 3 and giving both electrons to carbon 2 are an acylium cation and an enolate anion. These synthons are replaced by "synthetic equivalents" or "precursors" in the forward synthesis, namely two ethyl acetate molecules.

Offline narin

  • New Member
  • **
  • Posts: 6
  • Mole Snacks: +0/-0
Re: Retron?
« Reply #3 on: January 17, 2012, 01:05:22 AM »
Thank you OrgoTutor that was very helpful :) it makes sense with what i'm learning at the moment

Sponsored Links