Literature DB >> 25165504

A new and more powerfully activating diamine for practical and scalable enantioselective aldehyde crotylsilylation reactions.

Linda M Suen1, Michael L Steigerwald1, James L Leighton1.   

Abstract

Entities:  

Year:  2013        PMID: 25165504      PMCID: PMC4142653          DOI: 10.1039/C3SC50714A

Source DB:  PubMed          Journal:  Chem Sci        ISSN: 2041-6520            Impact factor:   9.825


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  11 in total

1.  Catalytic, enantioselective addition of substituted allylic trichlorosilanes using a rationally-designed 2,2'-bispyrrolidine-based bisphosphoramide.

Authors:  S E Denmark; J Fu
Journal:  J Am Chem Soc       Date:  2001-09-26       Impact factor: 15.419

2.  Catalytic enantioselective addition of allylic organometallic reagents to aldehydes and ketones.

Authors:  Scott E Denmark; Jiping Fu
Journal:  Chem Rev       Date:  2003-08       Impact factor: 60.622

3.  Highly diastereo- and enantioselective reagents for aldehyde crotylation.

Authors:  Blaine M Hackman; Pamela J Lombardi; James L Leighton
Journal:  Org Lett       Date:  2004-11-11       Impact factor: 6.005

4.  Origins of stereoselectivity in strain-release allylations.

Authors:  Xiyun Zhang; Kendall N Houk; James L Leighton
Journal:  Angew Chem Int Ed Engl       Date:  2005-01-28       Impact factor: 15.336

5.  A more comprehensive and highly practical solution to enantioselective aldehyde crotylation.

Authors:  Hyunwoo Kim; Stephen Ho; James L Leighton
Journal:  J Am Chem Soc       Date:  2011-04-12       Impact factor: 15.419

6.  Asymmetric allyl- and crotylboration with the robust, versatile, and recyclable 10-TMS-9-borabicyclo[3.3.2]decanes.

Authors:  Carlos H Burgos; Eda Canales; Karl Matos; John A Soderquist
Journal:  J Am Chem Soc       Date:  2005-06-08       Impact factor: 15.419

7.  Enhanced anti-diastereo- and enantioselectivity in alcohol-mediated carbonyl crotylation using an isolable single component iridium catalyst.

Authors:  Xin Gao; Ian A Townsend; Michael J Krische
Journal:  J Org Chem       Date:  2011-03-04       Impact factor: 4.354

8.  Recent advances in the activation of boron and silicon reagents for stereocontrolled allylation reactions.

Authors:  Jason W J Kennedy; Dennis G Hall
Journal:  Angew Chem Int Ed Engl       Date:  2003-10-13       Impact factor: 15.336

9.  Scandium-catalyzed allylboration of aldehydes as a practical method for highly diastereo- and enantioselective construction of homoallylic alcohols.

Authors:  Hugo Lachance; Xiaosong Lu; Michel Gravel; Dennis G Hall
Journal:  J Am Chem Soc       Date:  2003-08-27       Impact factor: 15.419

10.  anti-Diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents.

Authors:  In Su Kim; Soo Bong Han; Michael J Krische
Journal:  J Am Chem Soc       Date:  2009-02-25       Impact factor: 15.419

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  10 in total

1.  Lewis Acidity of Bis(perfluorocatecholato)silane: Aldehyde Hydrosilylation Catalyzed by a Neutral Silicon Compound.

Authors:  Allegra L Liberman-Martin; Robert G Bergman; T Don Tilley
Journal:  J Am Chem Soc       Date:  2015-04-16       Impact factor: 15.419

2.  Evolution of an Efficient and Scalable Nine-Step (Longest Linear Sequence) Synthesis of Zincophorin Methyl Ester.

Authors:  Liang-An Chen; Melissa A Ashley; James L Leighton
Journal:  J Am Chem Soc       Date:  2017-03-15       Impact factor: 15.419

3.  Total Synthesis and Structural Reassignment of Lyngbyaloside C Highlighted by Intermolecular Ketene Esterification.

Authors:  Chia-Fu Chang; Eric Stefan; Richard E Taylor
Journal:  Chemistry       Date:  2015-06-23       Impact factor: 5.236

4.  Direct, Mild, and General n-Bu4NBr-Catalyzed Aldehyde Allylsilylation with Allyl Chlorides.

Authors:  Makeda A Tekle-Smith; Kevin S Williamson; Isaac F Hughes; James L Leighton
Journal:  Org Lett       Date:  2017-11-03       Impact factor: 6.005

5.  A highly step-economical synthesis of dictyostatin.

Authors:  Stephen Ho; Cyril Bucher; James L Leighton
Journal:  Angew Chem Int Ed Engl       Date:  2013-05-10       Impact factor: 15.336

6.  Scalable synthesis of bryostatin 1 and analogs, adjuvant leads against latent HIV.

Authors:  Paul A Wender; Clayton T Hardman; Stephen Ho; Matthew S Jeffreys; Jana K Maclaren; Ryan V Quiroz; Steven M Ryckbosch; Akira J Shimizu; Jack L Sloane; Matthew C Stevens
Journal:  Science       Date:  2017-10-13       Impact factor: 47.728

7.  A thiocyanopalladation/carbocyclization transformation identified through enzymatic screening: stereocontrolled tandem C-SCN and C-C bond formation.

Authors:  G Malik; R A Swyka; V K Tiwari; X Fei; G A Applegate; D B Berkowitz
Journal:  Chem Sci       Date:  2017-10-03       Impact factor: 9.825

8.  Design and 22-step synthesis of highly potent D-ring modified and linker-equipped analogs of spongistatin 1.

Authors:  Linda M Suen; Makeda A Tekle-Smith; Kevin S Williamson; Joshua R Infantine; Samuel K Reznik; Paul S Tanis; Tyler D Casselman; Dan L Sackett; James L Leighton
Journal:  Nat Commun       Date:  2018-11-09       Impact factor: 14.919

9.  Synthesis of the C1-C27 Fragment of Stambomycin D Validates Modular Polyketide Synthase-Based Stereochemical Assignments.

Authors:  Jieyan Lim; Venkaiah Chintalapudi; Haraldur G Gudmundsson; Minh Tran; Alice Bernasconi; Araceli Blanco; Lijiang Song; Gregory L Challis; Edward A Anderson
Journal:  Org Lett       Date:  2021-09-08       Impact factor: 6.005

10.  Optimized Asymmetric Synthesis of Umuravumbolide.

Authors:  Marina Pérez-Palau; Eduard Balaguer-Garcia; Pedro Romea; Fèlix Urpí
Journal:  ACS Omega       Date:  2022-08-25
  10 in total

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