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10,786 Newest Publications in organic lettersrss
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15-Dec-2017 | Yuanxian Wang; Thomas R. Hoye, Organic Letters, 2017
Organic Letters DOI: 10.1021/acs.orglett.7b03436
15-Dec-2017 | Yasuhiro Meguro; Masato Noguchi; Gefei Li; Shin-ichiro Shoda, Organic Letters, 2017
Organic Letters DOI: 10.1021/acs.orglett.7b03400
15-Dec-2017 | Bijay Bhattarai; Pavel Nagorny, Organic Letters, 2017
A concise and scalable enantioselective total synthesis of the natural cardenolides cannogenol and cannogenol-3-O-α-l-rhamnoside has been achieved in 18 linear steps. The synthesis features a Cu(II)-catalyzed enantioselective and diastereoselective Michael reaction/tandem aldol cyclization and a ...
15-Dec-2017 | Ye Ri Han; Su-Hyang Shim; Dong-Su Kim; Chul-Ho Jun, Organic Letters, 2017
Organic Letters DOI: 10.1021/acs.orglett.7b03654
15-Dec-2017 | Nianyu Huang; Hongze Liao; Hui Yao; Tianpeng Xie; Shasha Zhang; Kun Zou; Xue-Wei Liu, Organic Letters, 2017
Organic Letters DOI: 10.1021/acs.orglett.7b03062
15-Dec-2017 | Christoph Priem; Armin Geyer, Organic Letters, 2017
Organic Letters DOI: 10.1021/acs.orglett.7b03525
15-Dec-2017 | Yun-Xuan Tan; Xiao-Qi Tang; Ping Liu; De-Shen Kong; Ya-Li Chen; Ping Tian; Guo-Qiang Lin, Organic Letters, 2017
The CuH-catalyzed asymmetric intramolecular reductive coupling of allenes to enones is successfully realized, providing cis-hydrobenzofurans with promising yields and excellent enantioselectivities. Such brilliant enantioselectivities are partially contributed by CuH-catalyzed favorable kinetic ...
15-Dec-2017 | Aaron Gerwien; Till Reinhardt; Peter Mayer; Henry Dube, Organic Letters, 2017
Organic Letters DOI: 10.1021/acs.orglett.7b03574
14-Dec-2017 | Wei Xiao; Qian-Qian Yang; Zhi Chen; Qin Ouyang; Wei Du; Ying-Chun Chen, Organic Letters, 2017
Organic Letters DOI: 10.1021/acs.orglett.7b03598
14-Dec-2017 | Truong N. Nguyen; Jeremy A. May, Organic Letters, 2017
GaCl3 and (IPr)GaCl3/AgSbF6 formed γ-tertiary and γ-quaternary carbons via homoconjugate addition of organoboron nucleophiles to diester- and ketone-functionalized cyclopropanes. Electron donor group cyclopropane substituents were not needed, allowing electron-deficient aryl, alkenyl, alkyl, and ...