188180-39-4Relevant academic research and scientific papers
Synthesis of novel asymmetrical single-chain phosphoglycol-based bolaamphiphiles
Drescher, Simon,Dobner, Bodo
supporting information, p. 564 - 573 (2014/01/23)
The synthesis of long-chain 1,ω-diols with orthogonal cleavable protecting groups can be effectively performed with the use of the Grignard coupling reaction, successfully leading to the preparation of novel asymmetrical single-chain phosphoglycol-based bolaamphiphiles-a side-product that always occurred during the synthesis of symmetrical bolalipids.
Formal synthesis of (+)-didemniserinolipid B
Mahipal, Bodugam,Mallikarjun, Kundarapu,Chandrasekhar, Srivari
, p. 45 - 47 (2012/01/14)
The formal synthesis of (+)-didemniserinolipid B is achieved using Weinreb reaction, Yadav's chiral propargyl alcohol protocol and hydrolytic ketal formation as the key steps.
Quinol fatty alcohols as promoters of axonal growth
Hanbali, Mazen,Vela-Ruiz, Marta,Bagnard, Dominique,Luu, Bang
, p. 2637 - 2640 (2007/10/03)
The synthesis of three series of quinol fatty alcohols (QFAs) and their biological activities on the promotion of axonal growth are described. Interestingly, the 15-(2,5-dimethoxyphenyl)pentadecan-1-ol, the QFA bearing 15 carbon atoms on the side chain (n = 15), shows the most potent promotion of axonal growth in the presence of both permissive and non-permissive naturally occurring substrates such as Sema3A and myelin proteins.
Design and synthesis of hapten to induce phospholipase A2-like catalytic antibody
Isomura, Shigeki,Haruna, Mitsumasa,Kazuo, Ito
, p. 251 - 254 (2007/10/03)
Haptens 1a and 1b, transition-state analogs inducing phospholipase A2-like catalytic antibody, were synthesized. Hapten 1a inhibited hydrolysis of the sn-2 ester of phospholipid.
