186641-79-2Relevant articles and documents
Formal total synthesis of mandelalide A
Yamini,Reddy, K Mahender,Krishna, A Shiva,Lakshmi,Ghosh, Subhash
, (2019/03/23)
Abstract: In this article the formal total synthesis of mandelalide A has been described in details. The highly convergent and flexible strategy developed for mandelalide A involved the construction of key building blocks ent-9 and 7, and their assembly t
Synthesis of proposed aglycone of mandelalide A
Reddy, Karla Mahender,Yamini, Vanipenta,Singarapu, Kiran K.,Ghosh, Subhash
supporting information, p. 2658 - 2660 (2014/06/09)
A highly convergent synthesis of the proposed mandelalide A aglycone is reported. The cornerstones of the synthetic strategy include the following: E-selective intramolecular Heck cyclization, Masamune-Roush olefination, Stork-Zhao-Wittig olefination, mod
Synthesis of stereopure acyclic 1,5-dimethylalkane chirons: Building blocks of highly methyl-branched natural products
Li, Nan-Sheng,Piccirilli, Joseph A.
, p. 9633 - 9641 (2013/10/22)
An efficient synthetic method towards stereopure acyclic 1,5-dimethylalkane building blocks from methyl (2R)-3-hydroxy-2-methylpropionate (R)-1 (>99% ee) and methyl (2S)-3-hydroxy-2-methylpropionate (S)-1 (>99% ee) through a series of chemical transformat