Design and Synthesis of Chiral Oxathiozinone Scaffolds: Efficient Synthesis of Hindered Enantiopure Sulfinamides and Sulfinyl Ketimines

Zhengxu S. Han; Melissa A. Herbage; Hari P. R. Mangunuru; Yibo Xu; Li Zhang; Jonathan T. Reeves; Joshua D. Sieber; Zhibin Li; Philomen DeCroos; Yongda Zhang; Guisheng Li; Ning Li; Shengli Ma; Nelu Grinberg; Xiao‐jun Wang; Navneet Goyal; Dhileep Krishnamurthy; Bruce Z. Lu; Jinhua J. Song; Guijun Wang; Chris H. Senanayake

doi:10.1002/anie.201301676

Ask about this paper

Answers are grounded in this paper and cite their sources.

Abstract

Is that SO? The title scaffolds have a highly active and properly differentiated SO bond for the efficient synthesis of enantiopure sulfinamides. The method is practical, green, and has the potential to provide an economical commercial process for the synthesis of bulky sulfinamides.

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Han et al. (2013) studied this question.

synapsesocial.com/papers/6a70242e5d37378ac1dd36a8 https://doi.org/10.1002/anie.201301676

View at Publisher

Ask AI

Bookmark

Share

Design and Synthesis of Chiral Oxathiozinone Scaffolds: Efficient Synthesis of Hindered Enantiopure Sulfinamides and Sulfinyl Ketimines

Ask about this paper

Abstract

Discussion

Cite This Study

Design and Synthesis of Chiral Oxathiozinone Scaffolds: Efficient Synthesis of Hindered Enantiopure Sulfinamides and Sulfinyl Ketimines

Ask about this paper

Abstract

Discussion

Cite This Study

Keep reading

Keep reading