On-DNA Transfer Hydrogenolysis and Hydrogenation for the Synthesis of DNA-Encoded Chemical Libraries.
On-DNA Transfer Hydrogenolysis and Hydrogenation for the Synthesis of DNA-Encoded Chemical Libraries.
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DNA转移氢解和氢化,用于合成DNA编码的化学文库。
DOI:
10.1002/anie.202111927
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发表时间:
2022-01-17
影响因子:
16.6
通讯作者:
Waring, Michael J.
中科院分区:
文献类型:
--
作者:
Stanway-Gordon, Harriet A.;Graham, Jessica S.;Waring, Michael J.
DNA‐encoded libraries (DELs) are an increasingly popular approach to finding small molecule ligands for proteins. Many DEL synthesis protocols hinge on sequential additions of monomers using split‐pool combinatorial methods. Therefore, compatible protecting group strategies that allow the unmasking of reactive functionality (e. g. amines and alcohols) prior to monomer coupling, or the removal of less desirable functionality (e. g., alkenes and alkynes) are highly desirable. Hydrogenation/hydrogenolysis procedures would achieve these ends but have not been amenable to DEL chemistry. We report a catalytic hydrogen transfer reaction using Pd/C, HCONH4 and the micelle‐forming surfactant, TPGS‐750‐M, which gives highly efficient conversions for hydrogenolysis of Cbz‐protected amines and benzyl protected alcohols and hydrogenation of nitros, halides, nitriles, aldehydes, alkenes and alkynes. Application to multicycle synthesis of an encoded compound was fully compatible with DNA‐amplification and sequencing, demonstrating its applicability to DEL synthesis. This method will enable synthetic DEL sequences using orthogonal protecting groups. A catalytic hydrogen transfer reaction using Pd/C, HCONH4 and the micelle‐forming surfactant, TPGS‐750‐M for hydrogenolysis of Cbz‐protected amines and benzyl protected alcohols and hydrogenation of alkenes, alkynes, nitros, nitriles, halides and aldehydes of DNA‐conjugated substrates is described. The methodology is fully compatible with DNA‐amplification and sequencing, demonstrating its applicability to DEL synthesis. This method will enable synthetic DEL sequences using orthogonal protecting groups.
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影响因子:
3.6
作者:
Lipshutz, Bruce H.;Ghorai, Subir;Abela, Alexander R.;Moser, Ralph;Nishikata, Takashi;Duplais, Christophe;Krasovskiy, Arkady;Gaston, Ricky D.;Gadwood, Robert C.
通讯作者:
Gadwood, Robert C.
影响因子:
15
作者:
Yuen, Lik Hang;Dana, Srikanta;Franzini, Raphael M.
通讯作者:
Franzini, Raphael M.
影响因子:
3.2
作者:
Belyanskaya, Svetlana L.;Ding, Yun;Israel, David I.
通讯作者:
Israel, David I.
DOI:
10.1073/pnas.89.12.5381
发表时间:
1992-06-15
影响因子:
11.1
作者:
BRENNER, S;LERNER, RA
通讯作者:
LERNER, RA
影响因子:
4.7
作者:
Priego, Julian;de Pedro Beato, Eduardo;Torrado, Alicia
通讯作者:
Torrado, Alicia