28Mar/123
A Little Self Deprecation in Tetrahedron
This caught my eye while reading Tetrahedron this morning. At first I thought it was a mistake, but then I realised that it was also in the PDF as well, presumably okayed by the authors. I think it's pretty funny to see this title in the TOC with 'Orginal Research Article' next to it:
Strangely, the rest of the paper seems quite confident. I guess time will tell.
Filed under: Ask the audience, Current Literature, Fun
Leave a comment
Reference Resovler
Recent Comments
- Fernando on Woodward Wednesday 6: Reserpine (Part 2/2)
- Brandon on Guest Post: Pactamycin (Hanessian, 2012)
- Berk on And Now For Something Completely Different 7: XKCD-style Venn Diagrams
- mass_speccer on And Now For Something Completely Different 6: Green Chemistry
- BRSM on And Now For Something Completely Different 7: XKCD-style Venn Diagrams
- Hadriel on And Now For Something Completely Different 7: XKCD-style Venn Diagrams
- Haha on And Now For Something Completely Different 6: Green Chemistry
- Steve on And Now For Something Completely Different 6: Green Chemistry
- vinylogous on And Now For Something Completely Different 6: Green Chemistry
- gippgig on And Now For Something Completely Different 6: Green Chemistry
Archives
- [+] 2013 (13)
- [+] 2012 (54)
- [+] 2011 (48)
All Time Most Popular
- (-)-Acetylaranotin - 110,468 views
- Conditions You’ll Probably Never be Desperate Enough to Try - 39,232 views
- Drugs I Shan’t Be Taking This Week 1: 2,4-Dinitrophenol - 30,530 views
- Where Did It All Go Wrong? - 22,940 views
- Kibdelone C - 17,910 views
- ‘No Added Metals’ Is The New ‘Metal Free’ - 15,830 views
- And Now For Something Completely Different 4: Wikipedia Fun - 12,672 views
- Woodward Wednesday 3: Chlorophyll a - 11,672 views
Tags
Aldol
arylation
Aryne
Axinellamines
azide
Baran
bromination
carreira
carvone
Cephalosporin C
colouring competition
Corey
Cubane
Decarboxylative alkylation
Diels-Alder
Eaton
Finkelstein
Garg
Heck
Hydrogenation
indolyne
Liphagal
Literature
Macrodiolide
Mulvember
mulzer
Negishi
Nicolaou
Palladium
Pauson-Khand
protecting groups
RCM
Sonogashira
Stoltz
strychnine
Taxadiene
Taxol
Thiocarbonyl diimidazole
thiourea
TNT
total synthesis
Wender
woodward
Woodward Wednesday
Yamaguchi
Categories
- ANFSCD (7)
- Ask the audience (19)
- BRSM Reviews (2)
- Current Literature (52)
- Fun (20)
- Guest Post (2)
- Lab (4)
- Literature (35)
- Mulvember (3)
- Named reactions (12)
- Not Chemistry (8)
- Serious (18)
- Top 5 (3)
- Total Synthesis (48)
- Uncategorized (5)
- Woodward Wednesdays (9)
- WWWTP (2)
Links
- A Retrosynthetic Life
- All Things Metathesis
- Chembark
- Chemical Connections
- Chemically Active
- Chemistry Blog
- Chemistry By Design
- Chemjobber
- Doctor Galactic and The Labcoat Cowboy
- In The Pipeline
- Just Like Cooking
- Master Organic Chemistry
- Natural Product Man
- New Reactions
- Not The Lab (NTL)
- Org. Prep. Daily
- Organic Chemistry Techniques and Tips
- Synthetic Nature
- Synthetic Remarks
- Tenderbutton Archive
- The Chemistry Cascade
- The Heterocyclist
- The Organic Solution
- The Organometallic Reader
- TOCROFL
- Totally Synthetic


April 3rd, 2012 - 13:24
At least their reagents are the right way up:
http://pubs.acs.org/doi/abs/10.1021/jo3001854
April 4th, 2012 - 20:27
IMHO, this is only a mistranslation. I know for sure that Frenchies are far from being all fluent in English (I know my people) so that probably meant to be “a few” or “some”.
April 5th, 2012 - 08:02
Yeah, I think you’re probably right. A French girl in my lab often makes this mistake (saying ‘few’ instead of ‘a few’). It is funny to be invited out for ‘few beers’ after a viva, though!