Literature DB >> 22623437

A robust, efficient, and highly enantioselective method for synthesis of homopropargyl amines.

Erika M Vieira1, Fredrik Haeffner, Marc L Snapper, Amir H Hoveyda.   

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Year:  2012        PMID： 22623437      PMCID： PMC3787540          DOI： 10.1002/anie.201202694

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  23 in total

1.  One-pot three-component catalytic enantioselective synthesis of homoallylboronates.

Authors:  Ismail Ibrahem; Palle Breistein; Armando Córdova
Journal:  Angew Chem Int Ed Engl       Date:  2011-10-18       Impact factor: 15.336

2.  A catalytic asymmetric borono variant of Hosomi-Sakurai reactions with N,O-aminals.

Authors:  Yi-Yong Huang; Ananya Chakrabarti; Naohide Morita; Uwe Schneider; Shū Kobayashi
Journal:  Angew Chem Int Ed Engl       Date:  2011-10-04       Impact factor: 15.336

3.  Site- and enantioselective formation of allene-bearing tertiary or quaternary carbon stereogenic centers through NHC-Cu-catalyzed allylic substitution.

Authors:  Byunghyuck Jung; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2012-01-03       Impact factor: 15.419

Review 4.  The world of beta- and gamma-peptides comprised of homologated proteinogenic amino acids and other components.

Authors:  Dieter Seebach; Albert K Beck; Daniel J Bierbaum
Journal:  Chem Biodivers       Date:  2004-08       Impact factor: 2.408

5.  Enantioselective synthesis of boron-substituted quaternary carbons by NHC-Cu-catalyzed boronate conjugate additions to unsaturated carboxylic esters, ketones, or thioesters.

Authors:  Jeannette M O'Brien; Kang-sang Lee; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2010-08-11       Impact factor: 15.419

6.  Streamlined syntheses of (-)-dictyostatin, 16-desmethyl-25,26-dihydrodictyostatin, and 6-epi-16-desmethyl-25,26-dihydrodictyostatin.

Authors:  Wei Zhu; María Jiménez; Won-Hyuk Jung; Daniel P Camarco; Raghavan Balachandran; Andreas Vogt; Billy W Day; Dennis P Curran
Journal:  J Am Chem Soc       Date:  2010-07-07       Impact factor: 15.419

7.  On the interactivity of complex synthesis and tumor pharmacology in the drug discovery process: total synthesis and comparative in vivo evaluations of the 15-aza epothilones.

Authors:  S J Stachel; C B Lee; M Spassova; M D Chappell; W G Bornmann; S J Danishefsky; T C Chou; Y Guan
Journal:  J Org Chem       Date:  2001-06-15       Impact factor: 4.354

8.  A modular, efficient, and stereoselective synthesis of substituted piperidin-4-ols.

Authors:  Li Cui; Chaoqun Li; Liming Zhang
Journal:  Angew Chem Int Ed Engl       Date:  2010-11-22       Impact factor: 15.336

9.  Highly diastereoselective zinc-catalyzed propargylation of tert-butanesulfinyl imines.

Authors:  Daniel R Fandrick; Courtney S Johnson; Keith R Fandrick; Jonathan T Reeves; Zhulin Tan; Heewon Lee; Jinhua J Song; Nathan K Yee; Chris H Senanayake
Journal:  Org Lett       Date:  2010-02-19       Impact factor: 6.005

10.  Ruthenium-catalyzed oxidative cleavage of alkynes to carboxylic acids.

Authors:  Dan Yang; Fei Chen; Ze-Min Dong; Dan-Wei Zhang
Journal:  J Org Chem       Date:  2004-03-19       Impact factor: 4.354
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  13 in total

1.  N-Substituted tertiary and O-substituted quaternary carbon stereogenic centers by site-, diastereo- and enantioselective vinylogous Mannich reactions.

Authors:  Daniel L Silverio; Peng Fu; Emma L Carswell; Marc L Snapper; Amir H Hoveyda
Journal:  Tetrahedron Lett       Date:  2015-04-09       Impact factor: 2.415

2.  Electronically Activated Organoboron Catalysts for Enantioselective Propargyl Addition to Trifluoromethyl Ketones.

Authors:  Nicholas W Mszar; Malte S Mikus; Sebastian Torker; Fredrik Haeffner; Amir H Hoveyda
Journal:  Angew Chem Int Ed Engl       Date:  2017-06-21       Impact factor: 15.336

3.  Design, synthesis, and applications of chiral N-2-phenyl-2-propyl sulfinyl imines for group-assisted purification (GAP) asymmetric synthesis.

Authors:  Suresh Pindi; Jianbin Wu; Guigen Li
Journal:  J Org Chem       Date:  2013-03-26       Impact factor: 4.354

4.  A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core.

Authors:  Nicholas G W Cowper; Matthew J Hesse; Katie M Chan; Sarah E Reisman
Journal:  Chem Sci       Date:  2020-10-15       Impact factor: 9.825

5.  Simple organic molecules as catalysts for enantioselective synthesis of amines and alcohols.

Authors:  Daniel L Silverio; Sebastian Torker; Tatiana Pilyugina; Erika M Vieira; Marc L Snapper; Fredrik Haeffner; Amir H Hoveyda
Journal:  Nature       Date:  2013-02-14       Impact factor: 49.962

6.  NHC-Cu-catalyzed addition of propargylboron reagents to phosphinoylimines. Enantioselective synthesis of trimethylsilyl-substituted homoallenylamides and application to the synthesis of S-(-)-cyclooroidin.

Authors:  Nicholas W Mszar; Fredrik Haeffner; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2014-02-20       Impact factor: 15.419

7.  An efficient, practical, and enantioselective method for synthesis of homoallenylamides catalyzed by an aminoalcohol-derived, boron-based catalyst.

Authors:  Hao Wu; Fredrik Haeffner; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2014-03-03       Impact factor: 15.419

8.  A broadly applicable NHC-Cu-catalyzed approach for efficient, site-, and enantioselective coupling of readily accessible (pinacolato)alkenylboron compounds to allylic phosphates and applications to natural product synthesis.

Authors:  Fang Gao; James L Carr; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2014-01-28       Impact factor: 15.419

9.  Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.

Authors:  Charlotte A Osborne; Thomas B D Endean; Elizabeth R Jarvo
Journal:  Org Lett       Date:  2015-10-27       Impact factor: 6.005

10.  Copper-Catalyzed Enantioselective Addition of Styrene-Derived Nucleophiles to Imines Enabled by Ligand-Controlled Chemoselective Hydrocupration.

Authors:  Yang Yang; Ian B Perry; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2016-08-01       Impact factor: 15.419
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