Literature DB >> 21744824

Di-tert-butylisobutylsilyl, another useful protecting group.

Huan Liang1, Lin Hu, E J Corey.   

Abstract

The di-tert-butylisobutylsilyl (BIBS) protecting group offers new possibilities for synthetic processes because of its steric bulk, robustness of its derivatives, and other special properties.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID： 21744824     DOI： 10.1021/ol201640y

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  5 in total

1.  Siloxyl ether functionalized resins for chemoselective enrichment of carboxylic acids.

Authors:  Darci J Trader; Erin E Carlson
Journal:  Org Lett       Date:  2011-09-29       Impact factor: 6.005

2.  The supersilyl group as a carboxylic acid protecting group: application to highly stereoselective aldol and Mannich reactions.

Authors:  Jiajing Tan; Matsujiro Akakura; Hisashi Yamamoto
Journal:  Angew Chem Int Ed Engl       Date:  2013-05-29       Impact factor: 15.336

3.  Next-Generation Total Synthesis of Vancomycin.

Authors:  Maxwell J Moore; Shiwei Qu; Ceheng Tan; Yu Cai; Yuzo Mogi; D Jamin Keith; Dale L Boger
Journal:  J Am Chem Soc       Date:  2020-09-04       Impact factor: 15.419

4.  Synthesis and kinetics of disassembly for silyl-containing ethoxycarbonyls using fluoride ions.

Authors:  Eugene Camerino; Grant C Daniels; James H Wynne; Erick B Iezzi
Journal:  RSC Adv       Date:  2018-01-09       Impact factor: 3.361

Review 5.  The synthesis of functionalized bridged polycycles via C-H bond insertion.

Authors:  Jiun-Le Shih; Po-An Chen; Jeremy A May
Journal:  Beilstein J Org Chem       Date:  2016-05-17       Impact factor: 2.883
  5 in total

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