corpus.blog
41554 blogs · 4,417,066 posts Claim your blog
Record · corpus.blog/posts/01a0bb6c-cd29-7348-8901-531183fbcbcd

The Amide Functional Group: Properties, Synthesis, and Nomenclature

jamesash · published 28 February 2018

A record is what was published and who pointed at it. The text of the post is not held here: read it at the source, or at its Wayback capture.

Read the post at masterorganicchemistry.com Wayback capture
0blogs citing
First cited
—
Most recent
—
Rank this month
not ranked
Links from this post
28
Words captured
3,048

Cited by

No blog we hold has cited this post yet.

Links from this post

Link
Host
Reagent Friday: Sodium Amide (NaNH2) Read at the source ↗
masterorganicchemistry.com
https://www.masterorganicchemistry.com/2011/08/05/reagent-friday-lithium-di-isopropyl-amide-lda/
masterorganicchemistry.com
Conjugation And Resonance In Organic Chemistry Read at the source ↗
masterorganicchemistry.com
https://www.masterorganicchemistry.com/2011/05/06/simplifying-the-reactions-of-carboxylic-acid-derivatives-part-1/
masterorganicchemistry.com
https://cdn.masterorganicchemistry.com/wp-content/uploads/2019/12/Supp-1-Mechanism-of-the-schotten-baumann-reaction.gif
cdn.masterorganicchemistry.com
http://www.orgsyn.org/demo.aspx?prep=CV4P0760
orgsyn.org
https://cdn.masterorganicchemistry.com/wp-content/uploads/2022/08/Supp-2-Mechanism-of-DCC-coupling-of-amines-and-carboxylic-acids.gif
cdn.masterorganicchemistry.com
https://en.wikipedia.org/wiki/Epimer
en.wikipedia.org
What Makes A Good Leaving Group? Read at the source ↗
masterorganicchemistry.com
http://cenblog.org/the-haystack/2011/09/amides-humble-but-useful/
cenblog.org
https://en.wikipedia.org/wiki/Schotten%E2%80%93Baumann_reaction
en.wikipedia.org
https://twitter.com/carmendrahl?lang=en
twitter.com
https://www.sciencedirect.com/science/article/abs/pii/0040403980802280
sciencedirect.com
https://pubs.acs.org/doi/10.1021/jo048240a
pubs.acs.org
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cber.188401702178
chemistry-europe.onlinelibrary.wiley.com
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cber.188601902348
chemistry-europe.onlinelibrary.wiley.com
https://pubs.acs.org/doi/10.1021/ja204040k
pubs.acs.org
http://www.orgsyn.org/demo.aspx?prep=CV1P0099
orgsyn.org
https://pubs.acs.org/doi/10.1021/op700120n
pubs.acs.org
https://pubs.acs.org/doi/10.1021/ed036p182
pubs.acs.org
https://pubs.acs.org/doi/10.1021/ja01609a099
pubs.acs.org
https://pubs.acs.org/doi/10.1021/ja00957a027
pubs.acs.org
https://pubs.acs.org/doi/abs/10.1021/ja00957a028
pubs.acs.org
https://pubs.acs.org/doi/10.1021/cr60165a001
pubs.acs.org
http://orgsyn.org/demo.aspx?prep=CV7P0093
orgsyn.org
https://pubs.acs.org/doi/10.1021/ja00897a025
pubs.acs.org
https://pubs.acs.org/doi/10.1021/jo01351a600
pubs.acs.org
https://pubs.acs.org/doi/abs/10.1021/ja00784a041
pubs.acs.org