Short Convergent Synthesis of the Mycolactone Core Through Lithiation-Borylation Homologations.

نویسندگان

  • Christopher A Brown
  • Varinder K Aggarwal
چکیده

Using iterative lithiation-borylation homologations, the mycolactone toxin core has been synthesized in 13 steps and 17% overall yield. The rapid build-up of molecular complexity, high convergence and high stereoselectivity are noteworthy features of this synthesis.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Enantioselective synthesis of (R)-tolterodine using lithiation/borylation-protodeboronation methodology.

The synthesis of the pharmaceutical (R)-tolterodine is reported using lithiation/borylation-protodeboronation of a homoallyl carbamate as the key step. This step was tested with two permutations: an electron-neutral aryl Li-carbamate reacting with an electron-rich boronic ester and an electron-rich aryl Li-carbamate reacting with an electron-neutral boronic ester. It was found that the latter a...

متن کامل

Short Stereoselective Synthesis of the Phytophthora Universal Mating Hormone Alpha 1 using Lithiation/Borylation Reactions**

Alpha 1, the universal mating hormone of the virulent plant pathogen, Phytophthora, has been synthesized in 12 steps and 28% overall yield. Key C-C bond forming steps involved the use of two lithiation/borylation reactions to couple together enantioenriched building blocks, one of which also set up the stereochemistry at C11. Detailed analysis showed that the diastereomeric purity of the target...

متن کامل

Stereoselective total synthesis of (+)-giganin and its C10 epimer by using late-stage lithiation-borylation methodology.

The first total synthesis of (+)-giganin and its unnatural diastereoisomer (+)-C10-epi-giganin has been completed in a total of 13 linear steps, and 7 % and 8 % overall yield, respectively (see scheme; (-)-sp= (-)-sparteine, (+)-sps=(+)-sparteine surrogate). Lithiation-borylation methodology has been successfully applied in the key step, to couple together advanced intermediates with very high ...

متن کامل

Short stereoselective synthesis of the Phytophthora universal mating hormone α1 using lithiation/borylation reactions.

The universal mating hormone α 1 of the virulent plant pathogen Phytophthora has been synthesized in 12 steps and 28 % overall yield. Key CC bond-forming steps involved the use of two lithiation/borylation reactions to couple together enantioenriched building blocks, one of which also set up the stereochemistry of the tertiary alcohol at C11. Detailed analysis showed that the diastereomeric pu...

متن کامل

Application of the lithiation-borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenes.

The expedient enantioselective synthesis of 5 bisabolane sesquiterpenes has been achieved using a common, one-pot lithiation-borylation reaction of secondary benzylic carbamates and either protodeboronation or oxidation to give the natural products in fewer than 5 steps, with high yield and >94 : 6 er.

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Chemistry

دوره 21 40  شماره 

صفحات  -

تاریخ انتشار 2015