Literature DB >> 17902687

Nickel(0) triethyl phosphite complex-catalyzed allylic substitution with retention of regio- and stereochemistry.

Yasutaka Yatsumonji1, Yusuke Ishida, Akira Tsubouchi, Takeshi Takeda.   

Abstract

Nickel(0) triethyl phosphite complex-promoted reaction of allylic acetates with thiols produced allylic sulfides with retention of configuration without allylic rearrangement. A similar reaction of allylic acetates with alcohols and phenols also proceeded with retention of regio- and stereochemistry.

Entities:  

Year:  2007        PMID： 17902687     DOI： 10.1021/ol702122d

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


  3 in total

1.  Synthesis of Enantioenriched 3,4-Disubstituted Chromans through Lewis Base Catalyzed Carbosulfenylation.

Authors:  Travis Menard; Aragorn Laverny; Scott E Denmark
Journal:  J Org Chem       Date:  2021-10-21       Impact factor: 4.354

2.  Enantioselective, nickel-catalyzed Suzuki cross-coupling of quinolinium ions.

Authors:  Jason D Shields; Derek T Ahneman; Thomas J A Graham; Abigail G Doyle
Journal:  Org Lett       Date:  2013-11-26       Impact factor: 6.005

Review 3.  Transition metal catalyzed synthesis of aryl sulfides.

Authors:  Chad C Eichman; James P Stambuli
Journal:  Molecules       Date:  2011-01-17       Impact factor: 4.411
  3 in total

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