Roy, S., Schurmann, C. J., Mondal, T. et al. (2016). Activation of elemental sulfur at a two-coordinate platinum(0) center. Chemistry: A European Journal, 22(36), 12629-12633. DOI: 10.1002/chem.201603030 Back Cover, p. 12944. DOI: 10.1002/chem.201603552
Category: Chemistry
Exfoliated sheets of MoS2 trigger formation of aqueous gels with acute NIR light responsiveness
Singh, A., Kapil, N., Yenuganti, M., & Das, D. (2016). Exfoliated sheets of MoS2 trigger formation of aqueous gels with acute NIR light responsiveness. Chemical Communications, 52(97), 14043-14046. DOI: 10.1039/C6CC05734A
Efficient MoS2 exfoliation by cross-beta-amyloid nanotubes for multistimuli-responsive and biodegradable aqueous dispersions
Kapil, N., Singh, A., Singh, M., & Das, D. (2016). Efficient MoS2 exfoliation by cross-beta-amyloid nanotubes for multistimuli-responsive and biodegradable aqueous dispersions. Angewandte Chemie International Edition, 55(27), 7772-7776. DOI: 10.1002/anie.201509953
Approach to isoindolinones, isoquinolinones, and THIQs via Lewis acid-catalyzed Domino Strecker-lactamization/alkylations
Dhanasekaran, S., Suneja, A., Bisai, V. et al. (2016). Approach to isoindolinones, isoquinolinones, and THIQs via Lewis acid-catalyzed Domino Strecker-lactamization/alkylations. Organic Letters, 18(4), 634-637. DOI: 10.1021/acs.orglett.5b03331
Asymmetric syntheses of medicinally important isoindolinones (S)-PD 172938, (R)-JM 1232, and related
Suneja, A., Bisai, V., & Singh, V. K. (2016). Asymmetric syntheses of medicinally important isoindolinones (S)-PD 172938, (R)-JM 1232, and related. Journal of Organic Chemistry, 81(11), 4779-4788. DOI: 10.1021/acs.joc.6b00770