Issue 28, 2021

The mechanism of conversion of substituted glycals to chiral acenes via Diels–Alder reaction: a computational study

Abstract

Synthesis of linearly fused aromatic systems using a glycal-based diene with an aryne is a long-standing topic of interest in glycal chemistry. We have examined the mechanistic pathways for the transformation of substituted glycals to chiral fused aromatic cores via Diels–Alder (DA) reaction using the SMDACN-M06-2X/6-31G(d) level of theory. The DA reactions of E (1a) and Z (1a′) forms of C-2 alkenyl glycal and an aryl glycal (1b) as a diene were examined with a benzyne intermediate generated as a dienophile. The computational results reveal that 1a and 1b can only be transformed into the fused aromatic cores by the base-catalyzed reaction because a [1,5] sigmatropic hydrogen shift is not feasible. The activation free energy barrier for the base-catalyzed proton abstraction process is 4.2 kcal mol−1 and there is almost no barrier for stereoisomeric 1a DA-complexes. The activation free energy barrier values for stereoisomeric 1b DA-complexes for the base-catalyzed proton abstraction process are 10.8 and 12.4 kcal mol−1. The appropriate orientation of glycal-ring-oxygen and hydrogen at the 5th position of Z (1a′) forms of C-2 alkenyl glycal facilitates the [1,5] sigmatropic hydrogen shift; however, the base-catalyzed reaction is energetically more favored than the former case. The rate-determining step for 1a and 1a′ is the ring-opening step (18.2 and 19.5 kcal mol−1 for the S-stereoisomer), whereas the DA adduct formation step is the rate-determining step for 1b (16.1 kcal mol−1 for the S-stereoisomer). The structural analysis reveals the formation of the preferred S-stereoisomer over the R-stereoisomer with the respective dienes.

Graphical abstract: The mechanism of conversion of substituted glycals to chiral acenes via Diels–Alder reaction: a computational study

Supplementary files

Article information

Article type
Paper
Submitted
03 mars 2021
Accepted
28 juin 2021
First published
01 juil. 2021

Org. Biomol. Chem., 2021,19, 6353-6367

The mechanism of conversion of substituted glycals to chiral acenes via Diels–Alder reaction: a computational study

K. Jana, P. D. Wakchaure, N. Hussain, D. Mukherjee and B. Ganguly, Org. Biomol. Chem., 2021, 19, 6353 DOI: 10.1039/D1OB00408E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements