Comments on: Tot Syn was on holiday – and is three! http://totallysynthetic.com/blog/?p=1645 4,512 Ph. D. students died to make this blog... Thu, 09 Sep 2010 08:39:52 -0600 hourly 1 http://wordpress.org/?v=3.0 By: iamdeigo http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-273409 iamdeigo Sat, 05 Dec 2009 15:04:30 +0000 http://totallysynthetic.com/blog/?p=1645#comment-273409 congratulation! It is best blog by far! I hope you keep up your blog! congratulation! It is best blog by far! I hope you keep up your blog!

]]> By: Peter Kettler http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-251732 Peter Kettler Wed, 08 Jul 2009 13:52:33 +0000 http://totallysynthetic.com/blog/?p=1645#comment-251732 Thx for the great blog. I am a organometallic chemist by training working in industry by synthesizing PGM complexes for utilization in organic synthesis via homogeneous catalysis. I like to keep an eye on new trends and what to offer the synthetic organic chemistry world in terms of products for catalysis. Your blog on total synth provides great insight. All the best. Thx for the great blog. I am a organometallic chemist by training working in industry by synthesizing PGM complexes for utilization in organic synthesis via homogeneous catalysis. I like to keep an eye on new trends and what to offer the synthetic organic chemistry world in terms of products for catalysis. Your blog on total synth provides great insight. All the best.

]]> By: Chemist@ASU http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-238387 Chemist@ASU Fri, 15 May 2009 04:09:06 +0000 http://totallysynthetic.com/blog/?p=1645#comment-238387 hey, I can not believe you are not checking out JOC! They have solid synthetic papers (from time to time!). Both the RSC and ACS websites are a bit of a mess really. the rest you are spot on. keep up the good work. hey,

I can not believe you are not checking out JOC! They have solid synthetic papers (from time to time!).

Both the RSC and ACS websites are a bit of a mess really.

the rest you are spot on.

keep up the good work.

]]> By: Kevin http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-229908 Kevin Wed, 22 Apr 2009 15:17:32 +0000 http://totallysynthetic.com/blog/?p=1645#comment-229908 "La Jolla 1,094" Wow, that's at least 75% of the post-docs in KCN's lab! “La Jolla 1,094″

Wow, that’s at least 75% of the post-docs in KCN’s lab!

]]> By: ,,, http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-228290 ,,, Sat, 18 Apr 2009 16:50:28 +0000 http://totallysynthetic.com/blog/?p=1645#comment-228290 Hey, you just keep saying things! Explain and give references! Otherwise it sounds like bla-bla-bla... Hey, you just keep saying things! Explain and give references! Otherwise it sounds like bla-bla-bla…

]]> By: Luge http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-228268 Luge Sat, 18 Apr 2009 14:46:20 +0000 http://totallysynthetic.com/blog/?p=1645#comment-228268 What does a 1-hydroxy indole have to do with this? Their group references somei when appropriate (stephacidin). Ian you must be from ranier or overman or another group that was working on these. Bitter!! What does a 1-hydroxy indole have to do with this? Their group references somei when appropriate (stephacidin).

Ian you must be from ranier or overman or another group that was working on these. Bitter!!

]]> By: Ian http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-228186 Ian Sat, 18 Apr 2009 07:18:14 +0000 http://totallysynthetic.com/blog/?p=1645#comment-228186 no reference to Somei's work with 1-hydroxyindoles why does this guy think he invented everything? yawn no reference to Somei’s work with 1-hydroxyindoles

why does this guy think he invented everything? yawn

]]> By: antiaromatic http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-228168 antiaromatic Sat, 18 Apr 2009 05:36:29 +0000 http://totallysynthetic.com/blog/?p=1645#comment-228168 Yeah, I think it was a very bold step to hope that amide would form an equilibrium to a six membered ring when a five membered ring was already in place! I don't know that I would've ever proposed it or believed it could work if I didn't already see that it does. I guess the strain from the 5 membered ring is enough to make the equilibrium even exist...still extremely impressive. Yeah, I think it was a very bold step to hope that amide would form an equilibrium to a six membered ring when a five membered ring was already in place! I don’t know that I would’ve ever proposed it or believed it could work if I didn’t already see that it does. I guess the strain from the 5 membered ring is enough to make the equilibrium even exist…still extremely impressive.

]]> By: Luge http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-228165 Luge Sat, 18 Apr 2009 05:13:49 +0000 http://totallysynthetic.com/blog/?p=1645#comment-228165 Kapakahine = my fav synthesis of the year Kapakahine = my fav synthesis of the year

]]> By: ,,, http://totallysynthetic.com/blog/?p=1645&cpage=1#comment-228153 ,,, Sat, 18 Apr 2009 04:07:42 +0000 http://totallysynthetic.com/blog/?p=1645#comment-228153 DOI? DOI?

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