131380-48-8Relevant articles and documents
Synthesis of (-)- and (+)-Gummiferol via Asymmetric Synthesis of Glycidic Amides
García-Ruiz, Cristina,Cheng-Sánchez, Iván,Sarabia, Francisco
, p. 1655 - 1662 (2016)
An efficient synthesis of the natural product (-)-gummiferol is achieved according to a novel asymmetric methodology of epoxide formation based on a new class of chiral sulfonium salts. This new methodology allows the rapid and efficient construction of t
Stereoselective synthesis of the C3-C15 fragment of callyspongiolide
Reddy Ramidi, Gopal,Yadav, Jhillu S.,Mohapatra, Debendra K.
supporting information, p. 3579 - 3582 (2018/09/10)
The synthesis of C3-C15 fragment of callyspongiolide, a 14-membered macrolides isolated from the marine sponge Callyspongia sp., which was collected from the Indonesia, is reported. Highlights of the synthesis include construction of E-olefin through Juli
B(C6F5)3: A New Class of Strong and Bulky Lewis Acid for Exo-Selective Intermolecular Diels-Alder Reactions of Unreactive Acyclic Dienes with α,β-Enals
Zhou, Jia-Hui,Jiang, Bing,Meng, Fei-Fan,Xu, Yun-He,Loh, Teck-Peng
supporting information, p. 4432 - 4435 (2015/09/28)
Lewis acid B(C6F5)3 catalyzed the Diels-Alder reactions of multisubstituted open-chain dienes and α,β-enals to afford the desired products with high exo-selectivities are reported. The substituent effect of the dienes and dienophiles on the products stereoselectivity was thoroughly investigated, and it was found that most of the desired exo-Diels-Alder products could be obtained in good yields and with high exo-stereoselectivities.