Kannan Vaithegi, Kavirayani R. Prasad
Index: 10.1016/j.tet.2018.04.014
Full Text: HTML
A concise total synthesis of the macrolactone natural product Sch 725674 is accomplished starting from commercially available 2-deoxy-d-ribose. Pivotal reactions employed in the synthesis include the addition of 4-pentenylmagnesium bromide to the lactol derived from 2-deoxy-d-ribose, olefin cross metathesis and Yamaguchi macrolactonization.
Synthesis of chiral α-amino anilides via a DMEDA-promoted se...
2018-04-11 [10.1016/j.tet.2018.03.003] |
A site isolation-enabled organocatalytic approach to enantio...
2018-04-11 [10.1016/j.tet.2018.04.022] |
Chemoselectivity in the Kosugi-Migita-Stille coupling of bro...
2018-04-10 [10.1016/j.tet.2018.02.051] |
Process design methodology for organometallic chemistry in c...
2018-04-07 [10.1016/j.tet.2018.04.020] |
Substrate engineering: Effects of different N-protecting gro...
2018-04-07 [10.1016/j.tet.2018.04.012] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved