Synthesis of the Monomeric Unit of the Lomaiviticin Aglycon

Synthesis of the Monomeric Unit of the Lomaiviticin Aglycon

K. C. Nicolaou, Andrea L. Nold, and Hongming Li


Hello again,

it took some time to get this post done but I was again busy learning some mathematics and physical chemistry… Boring stuff…

But nevertheless here it is: the nice KCN approach to the relatively new class of Lomaiviticins A and B which structures reminds me somewhat of a class of compounds reviewed by Paul:

So what’s it all about with this class of compounds? As usual they exhibit an impressive activity against cancer cell lines through a novel type of action which is currently under investigation. They’re acting through cleavage of the DNA in cancer cells. Interesting stuff but let’s get started with the chemistry:

(As you can see I almost got my ChemDraw installed and it’s great… much better than this shitty ISIS Draw)


In this publication we’re dealing as mentioned above with the monomeric units of these two condensed polycycles. The retro is short and straightforward:


First the blue fragment:

They started with the readily available aldehyde which was debenzylated with AlCl3, oxidised to the p-quinone which was protected as the SEM-ether after reduction to give the blue fragment:

Scheme 1


The synthesis of the red fragment is also very short. Readily available ethyl-cyclohexenone was exposed to a Sharpless asymmetric dihydroxylation and protected as the acetonide. A Saegusa oxidation furnished a new double bond which is regioselectively iodinated:

Scheme 2


Now comes the interesting part: The union of the two fragments and the formation of the remaining five membered ring containing the unusual diazo-cyclopentadiene motif. Starting with an Ullmann coupling followed by a benzoin condensation using Rovis catalyst gives the almost finished product.

Scheme 3


They had some problems with the benzoin condensation in first instance by using this catalyst and a different naphthalene unit cause it lead to the formation of the Stetter product. This problem could be overcome by using the shown starting material under the same conditions.

Next a SmI2 induced hydroxyl transposition gives the almost functionalised intermediate. Again they had some problems with their own standard protocol from an older synthesis, so they modified and studied this reaction extensively and got good results with the following reaction sequence:

Scheme 4


Very cool stuff but I were wondering if they didn’t try to transpose the hydroxyl group through a chrome(VI) induced allylic oxidation followed by chemoselective reduction of the resulting ketone. Nevertheless a very effective reaction protocol.

At least they installed the diazo motif by forming the hydrazone with TsNHNH2 and oxidised it using Dess-Martin-periodinane which also cleaved the SEM-groups to give the expected quinone system. Reduction and subsequent acetylation, followed by SEM-ether cleavage with TMSOTf, oxidation using CAN and hydrolysis furnished the final product.

Scheme 5


This is a really short and effective approach to this exciting class of compounds, hopefully followed by the condensation of the monomers. Even though it is a typical KCN publication the extensive colouring is missing… Maybe he forgot it? Or they omitted it for clarity…

Suggestions are as usual welcome…


9 Responses

  1. Long time no post… 🙂

  2. yeah i know…
    i’m really busy these days with my studies and were on vacation last week…
    but i’m working on the hirsutellone synthesis from KCN…
    hopefully be finished this week-end

    stay tuned,
    thx for the comment

  3. oh i just saw paul was faster…
    hm… i will find something older that he’s been overlooked…

  4. yeah i understand…in fact I hadn’t been blogging for more than 2 years compared to your 2 months hiatus 🙂
    By the way, there is a really nice synthesis of Lupeol by Corey in JACS now 🙂

  5. hey, just “found” your blog again 😉 i visited it some time ago.
    nice stuff until you stopped blogging…
    will you be back again sometime? back to blog …
    … i’ll print the corey paper tomorrow 😉 if paul’s missing it i’ll take it (but probably he’s faster)

    stay tuned

  6. I have a new blog and now I blog in my native language with a purpose of promoting science in our own language…but lately I hadn’t been updating my new blog as well 🙂
    Too busy (lazy) with my research 🙂

  7. can I have a reference to your new blog?? whatever language you use.

  8. and why Haplophytine?

  9. hey my new blog is but i guess u won’t understand anything unfortunately…
    haplophytine is there just because it was the 1st molecule that came to my mind when i wanted to put smth on my avatar 🙂
    BTW, Paul scooped the Lupeol synthesis…again 🙂

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