Synthesis and reactivity of enediyne–nucleobase hybrids: effect of intramolecular π-stacking

Roy, Snigdha ; Bag, Subhendu Sekhar ; Basak, Amit (2012) Synthesis and reactivity of enediyne–nucleobase hybrids: effect of intramolecular π-stacking Tetrahedron, 68 (41). pp. 8600-8611. ISSN 0040-4020

Full text not available from this repository.

Official URL: http://doi.org/10.1016/J.Tet.2012.07.093

Related URL: http://dx.doi.org/10.1016/J.Tet.2012.07.093

Abstract

Three distinct classes of nucleobase-containing enediynes 1–9 with varying nature of the linker have been synthesized to explore the effect of π-stacking interaction in accelerating the rate of Bergman cyclization (BC). Chemical reactivity study, both experimental and computations demonstrated the important role that aromatic π-stacking interactions between the appended nucleobases within an enediyne frame play in lowering the activation barrier of Bergman cyclization.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:129893
Deposited On:02 Dec 2022 06:04
Last Modified:05 Dec 2022 05:27

Repository Staff Only: item control page