中国医学科学院药物研究所-九游官网下载

弓亚玲，博士，副研究员，硕士生导师。2006年毕业于日本国立岩手大学，获得博士学位，专业为有机化学。2009年10月至今在药物所合成室工作。2014年10月被聘为副研究员。

目前从事的研究方向包括：（1）生物活性的复杂天然产物的全合成，特别是具有笼状碳骨架天然产物目标分子合成。（2）有机合成策略及合成反应的研究。（3）创新药物研发。

1. asymmetric total synthesis of naphthospironone a. jiaxuan liu, shipeng zhang, fengsen sun, hui li, yaling gong*, shichao lu*, shu xu*, angw. chem. int, ed., 2023, 62(22), e202303229(1-4).
2. selective oxidation of benzylic and allylic alcohols with phi(oocf3)2/catalytic 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (ddq) under mild conditions. yi deng, shichao lu, lulu yue, yaling gong*, and xidong guan*, synthetic communications, 2022, 52(23), 2198-2204.
3. synthesis of fused purine heterocycles via a one-pot cascade reaction of a trisubstituted pyrimidine. bo liu#, yaling gong#, shichao lu, dandan li, huihong fan*, synlett, 2018, 29, 1796-1800.
4. separation of alkyne enantiomers by chiral column hplc analysis of their cobalt-complexes., qiaoyun liu, jing wang, junfei li, xiaolei wang, shichao lu, xuan li, yaling gong* and shu xu*. molecules., 2017, 22, 466.
5. benzimidazole-based compounds kill mycobacterium tuberculosis. european journal of medicinal chemistry., yaling gong#, selin somersan karakaya#, xiaoyong guo, purong zheng, ben gold, yao ma, david little, julia roberts, thulasi warrier, xiuju jiang, maneesh pingle, carl f. nathan**, gang liu*. 2014, 75, 336-353.
6. transition metal-free oxidative radical decarboxylation/cyclization for the construction of 6-alkyl/aryl phenanthridines., shichao lu, yaling gong, and demin zhou. the journal of organic chemistry., 2015, 80, 9336-9341.
7. use of unprotected amino acids in metal-free tandem radical cyclization reactions: divergent synthesis of 6-alkyl/acyl phenanthridines., shichao lu, hongshuang li, yaling gong, xiaolei wang, furong li, fei li, guiyun duan and shu xu., rsc advances, 2017, 7, 55891-55896.

1. 专利名称：苯并咪唑类化合物及其用途；发明人：刘刚，弓亚玲，carl f nathan, selin s karakaya. 授权公告号：cn 103333170b；授权公告日：2016.08.10