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14 in total

1. Vanadium-catalyzed oxidative Strecker reaction: α-C-H cyanation of para-methoxyphenyl (PMP)-protected primary amines.

Authors: Chen Zhu; Ji-Bao Xia; Chuo Chen
Journal: Tetrahedron Lett Date: 2014-01-01 Impact factor: 2.415

2. Synthetic utility of one-pot chemoenzymatic reaction sequences.

Authors: Tyler J Doyon; Alison R H Narayan
Journal: Synlett Date: 2019-06-06 Impact factor: 2.454

3. A Thioacetal Photocage Designed for Dual Release: Application in the Quantitation of Therapeutic Release by Synchronous Reporter Decaging.

Authors: Pamela T Wong; Shengzhuang Tang; Jayme Cannon; Jhindan Mukherjee; Danielle Isham; Kristina Gam; Michael Payne; Sean A Yanik; James R Baker; Seok Ki Choi
Journal: Chembiochem Date: 2016-11-30 Impact factor: 3.164

4. Room-temperature aromatization of tetrahydro-β-carbolines by 2-iodoxybenzoic acid: utility in a total synthesis of eudistomin U.

Authors: Joseph D Panarese; Stephen P Waters
Journal: Org Lett Date: 2010-09-17 Impact factor: 6.005

5. Oxone promoted dehydrogenative Povarov cyclization of N-aryl glycine derivatives: an approach towards quinoline fused lactones and lactams.

Authors: Devidas A More; Ganesh H Shinde; Aslam C Shaikh; M Muthukrishnan
Journal: RSC Adv Date: 2019-09-25 Impact factor: 4.036

New reactions of IBX: oxidation of nitrogen- and sulfur-containing substrates to afford useful synthetic intermediates.

1. Vanadium-catalyzed oxidative Strecker reaction: α-C-H cyanation of para-methoxyphenyl (PMP)-protected primary amines.

2. Synthetic utility of one-pot chemoenzymatic reaction sequences.

3. A Thioacetal Photocage Designed for Dual Release: Application in the Quantitation of Therapeutic Release by Synchronous Reporter Decaging.

4. Room-temperature aromatization of tetrahydro-β-carbolines by 2-iodoxybenzoic acid: utility in a total synthesis of eudistomin U.

5. Oxone promoted dehydrogenative Povarov cyclization of N-aryl glycine derivatives: an approach towards quinoline fused lactones and lactams.

6. Combinatorial synthesis of chemical building blocks 1. Azomethines.

7. Enantioselective total synthesis of (+)-ibophyllidine via an asymmetric phosphine-catalyzed [3 + 2] annulation.

8. Efficient preparation of aldoximes from arylaldehydes, ethylenediamine and Oxone in water.

9. Visible-light harvesting pyrene-based MOFs as efficient ROS generators.

10. C-H Activation Enables a Concise Total Synthesis of Quinine and Analogues with Enhanced Antimalarial Activity.