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The Expanded Genetic Alphabet

Angewandte Chemie (International ed.), 2015-10, Vol.54 (41), p.11930-11944

International ed. in English, 2015

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Natural-like Replication of an Unnatural Base Pair for the Expansion of the Genetic Alphabet and Biotechnology Applications

Journal of the American Chemical Society, 2014-01, Vol.136 (3), p.826-829

2014

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Systematic exploration of a class of hydrophobic unnatural base pairs yields multiple new candidates for the expansion of the genetic alphabet

Nucleic acids research, 2014-09, Vol.42 (16), p.10235

2014

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Efficient and sequence-independent replication of DNA containing a third base pair establishes a functional six-letter genetic alphabet

Proceedings of the National Academy of Sciences - PNAS, 2012-07, Vol.109 (30), p.12005-12010

2012

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Site-Specific Labeling of DNA and RNA Using an Efficiently Replicated and Transcribed Class of Unnatural Base Pairs

Journal of the American Chemical Society, 2011-12, Vol.133 (49), p.19878-19888

2011

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Vicinal Amino Alcohols as Organocatalysts in Asymmetric Cross-Aldol Reaction of Ketones: Application in the Synthesis of Convolutamydine A

Organic letters, 2007-12, Vol.9 (26), p.5473-5476

2007

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Major Groove Substituents and Polymerase Recognition of a Class of Predominantly Hydrophobic Unnatural Base Pairs

Chemistry : a European journal, 2012-01, Vol.18 (4), p.1231-1239

2012

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Solution Structure, Mechanism of Replication, and Optimization of an Unnatural Base Pair

Chemistry : a European journal, 2010-11, Vol.16 (42), p.12650-12659

2010

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Homogeneous Nickel Catalysts for the Selective Transfer of a Single Arylthio Group in the Catalytic Hydrothiolation of Alkynes

Organometallics, 2006-09, Vol.25 (19), p.4462-4470

2006

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Vanadium-Catalyzed Asymmetric Epoxidation of Allylic Alcohols in Water

Journal of organic chemistry, 2009-05, Vol.74 (9), p.3350-3355

2009

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A semi-synthetic organism with an expanded genetic alphabet

Nature (London), 2014-05, Vol.509 (7500), p.385-388

2014

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Nickel(II) Chloride-Catalyzed Regioselective Hydrothiolation of Alkynes

Advanced synthesis & catalysis, 2005-12, Vol.347 (15), p.1993-2001

2005

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PCR with an Expanded Genetic Alphabet

Journal of the American Chemical Society, 2009-10, Vol.131 (41), p.14620-14621

2009

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Structural Insights into DNA Replication without Hydrogen Bonds

Journal of the American Chemical Society, 2013-12, Vol.135 (49), p.18637-18643

2013

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KlenTaq polymerase replicates unnatural base pairs by inducing a Watson-Crick geometry

Nature chemical biology, 2012-07, Vol.8 (7), p.612

2012

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FRET Characterization of Complex Conformational Changes in a Large 16S Ribosomal RNA Fragment Site-Specifically Labeled Using Unnatural Base Pairs

ACS chemical biology, 2016-05, Vol.11 (5), p.1347-1353

2016

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Expanding the Scope of Replicable Unnatural DNA: Stepwise Optimization of a Predominantly Hydrophobic Base Pair

Journal of the American Chemical Society, 2013-04, Vol.135 (14), p.5408-5419

2013

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Das erweiterte genetische Alphabet

Angewandte Chemie, 2015-10, Vol.127 (41), p.12098-12113

2015

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Sila Morita−Baylis−Hillman Reaction of Cyclopropenes

Journal of the American Chemical Society, 2007-12, Vol.129 (48), p.14868-14869

2007

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Site-Specifically Arraying Small Molecules or Proteins on DNA Using An Expanded Genetic Alphabet

Chemistry : a European journal, 2013-10, Vol.19 (42), p.14205-14209

2013

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Palladium and platinum catalyzed hydroselenation of alkynes: SeH vs SeSe addition to CC bond

Journal of organometallic chemistry, 2003-08, Vol.679 (2), p.162-172

2003

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ChemInform Abstract: The Expanded Genetic Alphabet

ChemInform, 2015-11, Vol.46 (47), p.no-no

2015

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Das erweiterte genetische Alphabet

Angewandte Chemie, 2015-10, Vol.127 (41), p.12098-12113

2015

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Expansion of the genetic alphabet in vitro and in vivo

Malyshev, Denis A

2013

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ProQuest

ChemInform Abstract: Vanadium-Catalyzed Asymmetric Epoxidation of Allylic Alcohols in Water

ChemInform, 2009-09, Vol.40 (37), p.no-no

2009

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The Expanded Genetic Alphabet

Natural-like Replication of an Unnatural Base Pair for the Expansion of the Genetic Alphabet and Biotechnology Applications

Systematic exploration of a class of hydrophobic unnatural base pairs yields multiple new candidates for the expansion of the genetic alphabet

Efficient and sequence-independent replication of DNA containing a third base pair establishes a functional six-letter genetic alphabet

Site-Specific Labeling of DNA and RNA Using an Efficiently Replicated and Transcribed Class of Unnatural Base Pairs

Vicinal Amino Alcohols as Organocatalysts in Asymmetric Cross-Aldol Reaction of Ketones: Application in the Synthesis of Convolutamydine A

Major Groove Substituents and Polymerase Recognition of a Class of Predominantly Hydrophobic Unnatural Base Pairs

Solution Structure, Mechanism of Replication, and Optimization of an Unnatural Base Pair

Homogeneous Nickel Catalysts for the Selective Transfer of a Single Arylthio Group in the Catalytic Hydrothiolation of Alkynes

Vanadium-Catalyzed Asymmetric Epoxidation of Allylic Alcohols in Water

A semi-synthetic organism with an expanded genetic alphabet

Nickel(II) Chloride-Catalyzed Regioselective Hydrothiolation of Alkynes

PCR with an Expanded Genetic Alphabet

Structural Insights into DNA Replication without Hydrogen Bonds

KlenTaq polymerase replicates unnatural base pairs by inducing a Watson-Crick geometry

FRET Characterization of Complex Conformational Changes in a Large 16S Ribosomal RNA Fragment Site-Specifically Labeled Using Unnatural Base Pairs

Expanding the Scope of Replicable Unnatural DNA: Stepwise Optimization of a Predominantly Hydrophobic Base Pair

Das erweiterte genetische Alphabet

Sila Morita−Baylis−Hillman Reaction of Cyclopropenes

Site-Specifically Arraying Small Molecules or Proteins on DNA Using An Expanded Genetic Alphabet

Palladium and platinum catalyzed hydroselenation of alkynes: SeH vs SeSe addition to CC bond

ChemInform Abstract: The Expanded Genetic Alphabet

Das erweiterte genetische Alphabet

Expansion of the genetic alphabet in vitro and in vivo

ChemInform Abstract: Vanadium-Catalyzed Asymmetric Epoxidation of Allylic Alcohols in Water

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