J. Li

发表

Jacobsen-Katsuki epoxidation

J. Li, 2003 .

The Art of Drug Synthesis

J. Li, Douglas S. Johnson, 2007 .

Schmidt Rearrangement

J. Li, 2021, Name Reactions.

C-H Bond Activation in Organic Synthesis

J. Li, 2015 .

Bartoli indole synthesis

J. Li, 2009 .

Gould–Jacobs reaction

J. Li, 2009 .

Metal-Catalyzed Cross-Coupling Reactions for Indoles

G. Gribble, J. Li, 2010 .

Modern Organic Synthesis in the Laboratory

C. Limberakis, J. Li, D. Pflum, 2007 .

Myers-Saito cyclization

J. Li, 2009 .

Pd-Catalyzed C―H Functionalization

J. Li, 2015 .

Bedaquiline (Situro): A Diarylquinoline that Blocks Tuberculosis ATP Synthase for the Treatment of Multi‐Drug Resistant Tuberculosis

J. Li, Elizabeth N. Cruz, Amanda N. Moules, 2015 .

Applications of Palladium Chemistry to the Total Syntheses of Naturally Occurring Indole Alkaloids

J. Li, 1999 .

Criegee mechanism of ozonolysis

J. Li, 2003 .

Buchwald–Hartwig Amination

J. Li, 2021, Name Reactions.

Chapter 1 An introduction to palladium catalysis

J. Wolfe, J. Li, 2007 .

Buchwald-Hartwig C-N bond and C-O bond formation reactions

J. Li, 2002 .

Imide-Containing Synthetic Drugs

J. Li, 2019, Imides.

Quinazolinones and pyrido[3,4-d]pyrimidin-4-ones as orally active and specific matrix metalloproteinase-13 inhibitors for the treatment of osteoarthritis.

R. D. Dyer, Adam R. Johnson, R. Dyer, 2008, Journal of medicinal chemistry.

Smoothened antagonists for hair inhibition.

Danielle E. Dettling, V. Shanmugasundaram, M. Swaroop, 2010, Bioorganic & medicinal chemistry letters.

Name reactions for carbocyclic ring formations

E. Corey, J. Li, 2010 .

Thyroid receptor agonists for the treatment of androgenetic alopecia.

R. L. Dow, J. Li, L. Mitchell, 2010, Bioorganic & medicinal chemistry letters.

Criegee glycol cleavage

J. Li, 2009 .

Baeyer–Villiger Oxidation

J. Li, 2021, Name Reactions.

Anti-Inflammatory Drugs

J. Li, 2006 .

Negishi Cross-Coupling Reaction

J. Li, 2021, Name Reactions.

Suzuki–Miyaura Coupling

J. Li, 2021, Name Reactions.

Metal-Catalyzed Cross-Coupling Reactions for Indoles

G. Gribble, J. Li, 2011 .

Hiyama cross-coupling reaction

J. Li, 2002 .

Palladium in Quinoline Synthesis

J. Li, N. Ahmad, 2003 .

Laughing Gas, Viagra, and Lipitor: The Human Stories behind the Drugs We Use

J. Li, 2006 .

Henry Nitroaldol Reaction

J. Li, 2021, Name Reactions.

Synthesis and structure-activity relationship of 2-amino-3-heteroaryl-quinoxalines as non-peptide, small-molecule antagonists for interleukin-8 receptor.

D. T. Connor, B. Roth, S. Qin, 2003, Bioorganic & medicinal chemistry.

Large-Ring Carbocycles

J. Li, 2010 .

Temperature-dependent synthesis of metal-organic frameworks based on a flexible tetradentate ligand with bidirectional coordination donors.

S. Batten, Jianping Ma, Ru-Qi Huang, 2007, Journal of the American Chemical Society.

A bioinspired and biocompatible ortho-sulfiliminyl phenol synthesis

Wei‐Yin Sun, Yi Lu, Qian Wu, 2017, Nature Communications.

Abnormal Claisen rearrangement

J. Li, 2003 .

Small molecule interleukin-8 modulators

J. Li, 2001 .

Lorcaserin (Belviq): Serotonin 2C Receptor Agonist for the Treatment of Obesity

J. Li, Taylor D. Krueger, Emily S. Murzinski, 2015 .

Five-Membered Carbocycles

J. Li, 2010 .

Subject Index

J. Kastelik, J. Li, K. Moghissi, 1959, Sadhana.

Free radical chemistry of three-membered heterocycles

J. Li, 2001 .

Robinson–Schöpf reaction

J. Li, 2003 .

Modern Drug Synthesis: Li/Modern

J. Li, Douglas S. Johnson, 2010 .

Corey–Bakshi–Shibata (CBS) Reduction

J. Li, 2021, Name Reactions.

Corey–Bakshi–Shibata (CBS) reagent

J. Li, 2009 .

Lawesson’s Reagent

J. Li, 2021, Name Reactions.

Julia–Lythgoe Olefination

J. Li, 2021, Name Reactions.

Wharton oxygen transposition reaction

J. Li, 2002 .

SYNTHESIS OF 3-ARYL AND 3-HETEROCYCLIC QUINOXALIN-2-YLAMINES VIA PD-CATALYZED CROSS-COUPLING REACTIONS

J. Li, W. Yue, 1999 .

Stille Coupling

J. Li, 2021, Name Reactions.

Synthesis of 3‐Aryl and 3‐Heterocyclic Quinoxalin‐2‐ylamines via Pd‐Catalyzed Cross‐Coupling Reactions.

J. Li, W. Yue, 1999 .

Leuckart–Wallach Reaction

J. Li, 2021, Name Reactions.

Synthesis of Novel 3-Substituted Pyrrolo[2,3-b]quinoxalines via an Intramolecular Heck Reaction on an Aminoquinoxaline Scaffold.

J. Li, 1999, The Journal of organic chemistry.

Rhodium(III)-catalyzed C-H activation/[4+3] annulation of N-phenoxyacetamides and α,β-unsaturated aldehydes: an efficient route to 1,2-oxazepines at room temperature.

J. Zhao, J. Li, Liang Lu, 2014, Chemical communications.

Claisen isoxazole synthesis

J. Li, 2009 .

Claisen Condensation

J. Li, 2021, Name Reactions.

Chichibabin amination reaction

J. Li, 2002 .

Transformations of Carbocycles

J. Li, 2010 .

Boger pyridine synthesis

J. Li, 2003 .

NAME REACTIONS IN HETEROCYCLIC CHEMISTRY

E. Corey, J. Li, 2009 .

Copper(II)-Mediated ortho-Selective C(sp2)-H Tandem Alkynylation/Annulation and ortho-Hydroxylation of Anilides with 2-Aminophenyl-1H-pyrazole as a Directing Group.

J. Li, Wei Wang, W. Lee, 2018, The Journal of organic chemistry.

Name reactions for functional group transformations

E. Corey, J. Li, 2007 .

Barton–McCombie Deoxygenation

J. Li, 2021, Name Reactions.

Barton-McCombie deoxygenation

J. Li, 2009 .

Barton-McCombie deoxygenation reaction

J. Li, 2002 .

[1,2]-Wittig rearrangement

J. Li, 2014 .

A concise synthesis of all four possible benzo[4,5]furopyridines via palladium-mediated reactions.

J. Li, W. Yue, 2002, Organic letters.

Palladium-catalyzed electrophilic C–H fluorination of arenes using oxazoline as a removable directing group

J. Li, Yuning Shen, W. Lee, 2016 .

Wacker Oxidation

J. Li, 2021, Name Reactions.

Lossen Rearrangement

J. Li, 2021, Name Reactions.

Wolff-Kishner reduction

J. Li, 2002 .

Hajos–Wiechert Reaction

J. Li, 2021, Name Reactions.

Hajos-Wiechert reaction

J. Li, 2003 .

Leuckart-Wallach reaction

J. Li, 2009 .

Mukaiyama Michael Addition

J. Li, 2021, Name Reactions.

Biginelli Reaction

J. Li, 2021, Name Reactions.

Biginelli pyrimidone synthesis

J. Li, 2002 .

Dakin−West Reaction

J. Li, 2021, Name Reactions.

Robinson–Gabriel synthesis

J. Li, 2009 .

Pomeranz–Fritsch reaction

J. Li, 2002 .

Claisen, Eschenmoser-Claisen, Johnson-Claisen, and Ireland-Claisen rearrangements

J. Li, 2002 .

Hegedus indole synthesis

J. Li, 2002 .

2-Aminophenyl-1H-pyrazole as a Removable Directing Group for Copper-Mediated C-H Amidation and Sulfonamidation.

J. Li, Yuning Shen, W. Lee, 2016, Organic letters.

Stetter Reaction

J. Li, 2021, Name Reactions.

Stetter reaction (Michael-Stetter reaction)

J. Li, 2002 .

Di-π-methane rearrangement

J. Li, 2003 .

Strecker Amino Acid Synthesis

J. Li, 2021, Name Reactions.

Sonogashira Reaction

J. Li, 2021, Name Reactions.

Copper-Mediated sp2 C–H Chlorination with Trichloroacetamide Using a Removable Directing Group

J. Li, W. Lee, A. Tehrani, 2017 .

Rh(iii)-Catalyzed ortho-C-H alkynylation of N-phenoxyacetamides with hypervalent iodine-alkyne reagents at room temperature.

Qian Wu, J. Zhao, J. Li, 2017, Organic & biomolecular chemistry.

A redox-neutral catechol synthesis

Wei‐Yin Sun, Yi Lu, Qian Wu, 2017, Nature Communications.

Reissert reaction (aldehyde synthesis)

J. Li, 2003 .

Palladium-Catalyzed Direct C(sp2)-H ortho-Arylation of Anilides Using 2-Aminophenylpyrazole as the Directing Group.

J. Li, Yuning Shen, Wan-Chen Cindy Lee, 2017, The Journal of organic chemistry.

Ullmann Coupling

J. Li, 2021, Name Reactions.

Meyer–Schuster Rearrangement

J. Li, 2021, Name Reactions.

Pauson-Khand cyclopentenone synthesis

J. Li, 2003 .

Combes quinoline synthesis

J. Li, 2009 .

Michael Addition

J. Li, 2021, Name Reactions.

Heterocyclic chemistry in drug discovery

J. Li, 2013 .

Other Five-Membered Heterocycles

E. Corey, J. Li, 2004 .

Sakurai allylation reaction

J. Li, 2009 .

Sakurai allylation reaction (Hosomi-Sakurai reaction)

J. Li, 2003 .

Arndt-Eistert homologation

J. Li, 2003 .

Evans aldol reaction

J. Li, 2014 .

Hantzsch Dihydropyridine Synthesis

J. Li, 2021, Name Reactions.

Pechmann coumarin synthesis

J. Li, 2014 .

Pictet–Spengler Tetrahydroisoquinoline Synthesis

J. Li, 2021, Name Reactions.

Pictet-Spengler isoquinoline synthesis

J. Li, 2002 .

Bischler–Napieralski Reaction

J. Li, 2021, Name Reactions.

Stevens Rearrangement

J. Li, 2021, Name Reactions.

Li A3 reaction

J. Li, 2014 .

Palladium in Heterocyclic Chemistry: A Guide for the Synthetic Chemist

G. Gribble, J. Li, 2000 .

Doebner quinoline synthesis

J. Li, 2014 .

Chapter Four Applications of radical cyclization reactions in total syntheses of naturally occurring indole alkaloids

J. Li, 2001 .

Mannich Reaction

J. Li, 2021, Name Reactions.

Fischer Indole Synthesis

J. Li, 2021, Name Reactions.

Chan alkyne reduction

J. Li, 2014 .

Kröhnke Pyridine Synthesis

J. Li, 2021, Name Reactions.

ChemInform Abstract: Stereoselective Synthesis of syn- and anti-1,3- and 1,2-Dimethyl Arrays via Asymmetric Conjugate Additions.

David R. Williams, R. Mullins, J. Li, 2002 .

Total synthesis of myxovirescin A1

David R. Williams, J. Li, 1994 .

A synthesis of N-bridged 5,6-bicylic pyridines via a mild cyclodehydration using the burgess reagent and discovery of a novel carbamylsulfonylation reaction.

Jun Li, J. Li, H. Wong, 2008, Organic letters.

Barton–Zard reaction

J. Li, 2014 .

Hantzsch pyrrole synthesis

J. Li, 2009 .

Paal–Knorr Pyrrole Synthesis

J. Li, 2021, Name Reactions.

Gewald Aminothiophene Synthesis

J. Li, 2021, Name Reactions.

Diastereoselection in the conjugate additions of organocopper reagents to N-enoyloxazolidinones

David R. Williams, J. Li, Kissel William Scott, 1998 .

Name Reactions in Heterocyclic Chemistry: Li/Name Heterocyclic

E. Corey, J. Li, 2004 .

Zinin benzidine (semidne) rearrangement

J. Li, 2014 .

Zinin benzidine rearrangement (semidine rearrangement)

J. Li, 2002 .

Schmidt Rearrangement

J. Li, 2020, Name Reactions.

Meerwein–Ponndorf–Verley Reduction

J. Li, 2021, Name Reactions.

Mukaiyama Aldol Reaction

J. Li, 2021, Name Reactions.

Kolbe electrolytic coupling

J. Li, 2003 .

Noyori Asymmetric Hydrogenation

J. Li, 2021, Name Reactions.

Staudinger ketene cycloaddition

J. Li, 2009 .

Wittig Reaction

J. Li, 2021, Name Reactions.

Friedel–Crafts Reaction

J. Li, 2021, Name Reactions.

Ferrier Glycal Allylic Rearrangement

J. Li, 2021, Name Reactions.

AlMe(3)-promoted formation of amides from acids and amines.

J. Kadow, J. Li, Jianqing Li, 2012, Organic letters.

Cope elimination reaction

J. Li, 2003 .

Bamford–Stevens Reaction

J. Li, 2021, Name Reactions.

Chapter 3 – Palladium Chemistry in Pyridine Alkaloid Synthesis

J. Li, 2000 .

Skraup quinoline synthesis

J. Li, 2009 .

Von Richter reaction

J. Li, 2003 .

Meyers oxazoline method

J. Li, 2009 .

Diels-Alder reaction, inverse electronic demand Diels-Alder reaction, hetero-Diels-Alder reaction

J. Li, 2002 .

Corey-Bakshi-Shibata (CBS) reduction

J. Li, 2003 .

Larock indole synthesis

J. Li, 2002 .

Dötz Reaction

J. Li, 2021, Name Reactions.

Stork–Danheiser transposition

J. Li, 2014 .

Roush allylboronate reagent

J. Li, 2003 .

Schmidt’s trichloroacetimidate glycosidation

J. Li, 2014 .

Schmidt’s trichloroacetimidate glycosidation reaction

J. Li, 2009 .

Gassman indole synthesis

J. Li, 2009 .

[2,3]-Meisenheimer rearrangement

J. Li, 2009 .

Chan–Lam C–X Coupling Reaction

J. Li, 2021, Name Reactions.

Miyaura Borylation

J. Li, 2021, Name Reactions.

Name Reactions in Heterocyclic Chemistry II: Li/Name

E. Corey, J. Li, 2011 .

Ritter Reaction

J. Li, 2021, Name Reactions.

Kennedy oxidative cyclization

J. Li, 2003 .

Dowd–Beckwith ring expansion

J. Li, 2014 .

Dowd ring expansion

J. Li, 2003 .

de Mayo Reaction

J. Li, 2021, Name Reactions.

Robinson Annulation

J. Li, 2021, Name Reactions.

Alder Ene Reaction

J. Li, Jie Jack Li, 2021, Name Reactions.

Knoevenagel Condensation

J. Li, 2021, Name Reactions.

Kumada Reaction

J. Li, 2021, Name Reactions.

Kumada cross-coupling reaction

J. Li, 2003 .

Nozaki–Hiyama–Kishi Reaction

J. Li, 2021, Name Reactions.

Hoch-Campbell aziridine synthesis

J. Li, 2003 .

Gribble indole reduction

J. Li, 2003 .

Paal thiophene synthesis

J. Li, 2009 .

Dieckmann Condensation

J. Li, 2021, Name Reactions.

Polonovski–Potier Reaction

J. Li, 2021, Name Reactions.

Bouveault aldehyde synthesis

J. Li, 2009 .

Henry reaction (nitroaldol reaction)

J. Li, 2003 .

Dess–Martin periodinane oxidation

J. Li, 2009 .

Corey–Kim oxidation

J. Li, 2014 .

Benzoin Condensation

J. Li, 2021, Name Reactions.

Prins Reaction

J. Li, 2021, Name Reactions.

Keck stereoselective allylation

J. Li, 2003 .

Aldol Condensation

J. Li, 2021, Name Reactions.

Barton nitrite photolysis

J. Li, 2014 .

Rychnovsky polyol synthesis

J. Li, 2002 .

Fleming–Kumada oxidation

J. Li, 2009 .

Tamao-Kumada oxidation

J. Li, 2003 .

Tsuji-Trost Reaction

J. Li, 2021, Name Reactions.

Tsuji—Trost reaction

J. Li, 2002 .

[2,3]-Wittig rearrangement

J. Li, 2014 .

Sharpless Asymmetric Epoxidation

J. Li, 2021, Name Reactions.

Simmons–Smith Reaction

J. Li, 2021, Name Reactions.

Sharpless Asymmetric Amino-hydroxylation

J. Li, 2021, Name Reactions.

Darzens Condensation

J. Li, 2021, Name Reactions.

Corey–Chaykovsky reaction

J. Li, 2009 .

Williamson Ether Synthesis

J. Li, 2021, Name Reactions.

Barbier Reaction

J. Li, 2021, Name Reactions.

Corey–Seebach reaction

J. Li, 2014 .

Baker-Venkataraman rearrangement

J. Li, 2009 .

Darzens glycidic ester condensation

J. Li, 2003 .

Sharpless Asymmetric Dihydroxylation

J. Li, 2021, Name Reactions.

[1,2]-Meisenheimer rearrangement

J. Li, 2009 .

Dutt-wormall reaction

J. Li, 2002 .

Regitz diazo synthesis

J. Li, 2009 .

Cadiot–Chodkiewicz Coupling

J. Li, 2021, Name Reactions.

Borsche–Drechsel cyclization

J. Li, 2003 .

Blanc chloromethylation reaction

J. Li, 2003 .

Pictet–Gams isoquinoline synthesis

J. Li, 2009 .

Name Reactions: A Collection of Detailed Reaction Mechanisms

J. Li, Jie Jack Li, 2002 .

Shapiro Reaction

J. Li, 2021, Name Reactions.

Tiffeneau-Demjanov Rearrangement

J. Li, 2003 .

The Carcinogenicity of Aflatoxin B1

Mengxi Liu, J. Li, 2019, Aflatoxin B1 Occurrence, Detection and Toxicological Effects.

AN OVERVIEW OF SYNTHETIC STUDIES OF ANTIBIOTICS FROM MYXOBACTERIA

David R. Williams, J. Li, R. Hutchings, 2000 .

Baker–Venkataraman Rearrangement

J. Li, 2021, Name Reactions.

Houben-Hoesch Reaction

J. Li, 2021, Name Reactions.

Takai Reaction

J. Li, 2021, Name Reactions.

Single- and Multimagnon Dynamics in Antiferromagnetic $\alpha$-Fe$_2$O$_3$ Thin Films

J. Pelliciari, J. Kuneš, V. Bisogni, 2022, 2210.06911.

Pauson-Khand Reaction

J. Li, 2021, Name Reactions.

Contemporary Drug Synthesis: Li/Drug Synthesis

B. Roth, J. Li, Douglas S. Johnson, 2004 .

von Braun Reaction

J. Li, 2021, Name Reactions.

Jacobsen–Katsuki Epoxidation

J. Li, 2021, Name Reactions.

Algar— Flynn— Oyamada Reaction

J. Li, 2009 .

Corey–Nicolaou macrolactonization

J. Li, 2009 .

Swern Oxidation

J. Li, 2021, Name Reactions.

Hofmann Rearrangement

J. Li, 2021, Name Reactions.

Entecavir (Baraclude): A Carbocyclic Nucleoside for the Treatment for Chronic Hepatitis B

J. Li, 2015 .

Corey-Winter olefin synthesis

J. Li, 2003 .

Fujimoto-Belleau reaction

J. Li, 2003 .

Hofmann rearrangement (Hofmann degradation reaction)

J. Li, 2002 .

Feist–Bénary furan synthesis

J. Li, 2002 .

Brook Rearrangement

J. Li, 2021, Name Reactions.

Eschweiler–Clarke Reductive Amination

J. Li, 2021 .

Eschenmoser coupling reaction

J. Li, 2003 .

Zaitsev’s elimination rule

J. Li, 2014 .

Drug discovery : practices, processes, and perspectives

E. Corey, J. Li, 2013 .

Name Reactions: A Collection of Detailed Mechanisms and Synthetic Applications Fifth Edition

J. Li, 2006 .

Prévost trans-dihydroxylation

J. Li, 2009 .

Pummerer Rearrangement

J. Li, 2021, Name Reactions.

Nicolaou IBX dehydrogenation

J. Li, 2014 .

Michaelis–Arbuzov phosphonate synthesis

J. Li, 2009 .

Koch–Haaf carbonylation

J. Li, 2009 .

Doering-LaFlamme allene synthesis

J. Li, 2003 .

Mori–Ban indole synthesis

J. Li, 2009 .

Hinsberg synthesis of thiophene derivatives

J. Li, 2009 .

Amadori glucosamine rearrangement

J. Li, 2002 .

Mitsunobu Reaction

J. Li, 2021, Name Reactions.

Liebeskind-Srogl coupling

J. Li, 2002 .

Synthesis of Novel 3‐Substituted Pyrrolo[2,3‐b]quinoxalines via an Intramolecular Heck Reaction on an Aminoquinoxaline Scaffold.

J. Li, 2000 .

Heteroaryl Heck reaction

J. Li, 2002 .

Miyaura boration reaction

J. Li, 2020, Catalysis from A to Z.

Fiesselmann thiophene synthesis

J. Li, 2009 .

A practical Buchwald-Hartwig amination of 2-bromopyridines with volatile amines.

J. Li, L. Mitchell, Z. Wang, 2007, Journal of Organic Chemistry.

Birch Reduction

J. Li, 2021, Name Reactions.

Sandmeyer Reaction

J. Li, 2021, Name Reactions.

Modern Drug Synthesis

J. Li, Douglas S. Johnson, Jie Jack Li, 1994 .

Name Reactions: A Collection of Detailed Mechanisms and Synthetic Applications

J. Li, 2021 .

A Practical Buchwald—Hartwig Amination of 2‐Bromopyridines with Volatile Amines.

J. Li, L. Mitchell, Z. Wang, 2007 .

Davis chiral oxaziridine reagents

J. Li, 2002 .

Cadogan–Sundberg indole synthesis

J. Li, 2014 .

Total Synthesis of Natural Products: At the Frontiers of Organic Chemistry

E. Corey, J. Li, 2012 .

History of Drug Discovery

J. Li, 2013 .

Conrad–Limpach reaction

J. Li, 2014 .

Conrad-Lipach reaction

J. Li, 2002 .

Fischer-Hepp rearrangement

J. Li, 2002 .

Cannizzaro disproportionation reaction

J. Li, 2002 .

Hofmann-Martius reaction

J. Li, 2002 .

Markovnikov’s Rule

J. Li, 2021, Name Reactions.

Masamune-Roush conditions

J. Li, 2002 .

Protein tyrosine kinase inhibitors

B. Roth, J. Li, Douglas S. Johnson, 2004, Reactions weekly.

Vilsmeier-Haack Reaction

J. Li, 2021, Name Reactions.

Thermal reaction behavior of “red oil” decomposition products with HNO3

J. Li, Zheng Li, Lan Zhang, 2022, Journal of Radioanalytical and Nuclear Chemistry.

Benzilic Acid Rearrangement

J. Li, 2021, Name Reactions.

Boyland-Sims oxidation

J. Li, 2002 .

Allan-Robinson reaction

J. Li, 2002 .

Name Reactions for Homologations, Part II

J. Li, 2009 .

Contemporary Drug Synthesis

J. Li, 2004 .

Mislow–Evans rearrangement

J. Li, 2009 .

Hodges-Vedejs metallation of oxazoles

J. Li, 2003 .

Madelung indole synthesis

J. Li, 2002 .

Chichibabin Pyridine Synthesis

J. Li, 2021, Name Reactions.

Gomberg–Bachmann reaction

J. Li, 2002 .

C―H Activation

J. Li, 2019 .

Bergman Cyclization

J. Li, 2021, Name Reactions.

Corey—Fuchs reaction

J. Li, 2003 .

Still-gennari phosphonate reaction

J. Li, 2009 .

Horner–Wadsworth–Emmons Reaction

Jie Jack Li, J. Li, 2021, Name Reactions.

Reissert indole synthesis

J. Li, 2014 .

Rational design and synthesis of 4-((1R,2R)-2-hydroxycyclohexyl)-2(trifluoromethyl)benzonitrile (PF-998425), a novel, nonsteroidal androgen receptor antagonist devoid of phototoxicity for dermatological indications.

Danielle E. Dettling, T. R. Johnson, V. Shanmugasundaram, 2008, Journal of medicinal chemistry.

(1R,2S)-4-(2-cyano-cyclohexyl-oxy)-2-trifluoromethyl-benzonitrile, a potent androgen receptor antagonist for stimulating hair growth and reducing sebum production.

Danielle E. Dettling, T. R. Johnson, Mostofa A Hena, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of amino-pyridines as androgen receptor antagonists for stimulating hair growth and reducing sebum production.

Danielle E. Dettling, T. R. Johnson, T. Krieger-Burke, 2007, Bioorganic & Medicinal Chemistry Letters.

A New Approach for Ferrocenyl-Cyclopentenone and Ferrocenyl-Cyclopentenedione Compound Synthesis

Jianping Ma, Ru-Qi Huang, J. Li, 2008 .

Bucherer carbazole synthesis

J. Li, 2002 .

Hofmann—Löffler—Freytag reaction

J. Li, 2014 .

Morita–Baylis–Hillman Reaction

J. Li, 2021, Name Reactions.

Ivacaftor (Kalydeco): A CFTR Potentiator for the Treatment of Cystic Fibrosis

C. Lai, J. Li, T. Song, 2015 .

2,5-Bis-(sulfonyl)pyrazines as unprecedented building blocks and their SNAr reactions

J. Li, P. Cheng, Yong-Jin Wu, 2013 .

Ring-closing metathesis (RCM)

J. Li, 2009 .

Ring-closing metathesis (RCM) using Grubbs and Schrock catalysts

J. Li, 2003 .

Nickel-Catalyzed C―H Activation

J. Li, 2015 .

Blockbuster Drugs: The Rise and Decline of the Pharmaceutical Industry

J. Li, 2013 .

Guareschi-Thorpe condensation

J. Li, 2009 .

Buchner-Curtius-Schlotterbeck reaction

J. Li, 2003 .

Julia–Kocienski Olefination

J. Li, 2021, Name Reactions.

Tebbe olefination (Petasis alkenylation)

J. Li, 2003 .

Zhang enyne cycloisomerization

J. Li, 2014 .

Boulton–Katritzky rearrangement

J. Li, 2009 .

Gribble reduction of diaryl ketones

J. Li, 2002 .

Morgan–Walls reaction

J. Li, 2009 .

Morgan-Walls reaction (Pictet-Hubert reaction)

J. Li, 2003 .

Caspases in apoptosis and beyond

Junying Yuan, J. Li, J. Yuan, 2008, Oncogene.

Thorpe-Ziegler reaction

J. Li, 2002 .

Triumph of the Heart: The Story of Statins

J. Li, Jie Jack Li, 2009 .

Radical-Mediated C―H Bond Activation

J. Li, 2015 .

Brown Hydroboration

J. Li, 2021, Name Reactions.

Brown hydroboration reaction

J. Li, 2003 .

Fischer-Speier esterification

J. Li, 2014 .

Schotten-Baumann reaction

J. Li, 2002 .

Fischer oxazole synthesis

J. Li, 2014 .

Castro–Stephens coupling

J. Li, 2009 .

Willgerodt–Kindler reaction

J. Li, 2003 .

Yamada coupling reagent

J. Li, 2002 .

Medicinal Chemistry for Practitioners

J. Li, 2020 .

Cope, oxy-Cope, and anionic oxy-Cope rearrangements

J. Li, 2002 .

Ramberg–Bäcklund Reaction

J. Li, 2021, Name Reactions.

Hell-Volhardt-Zelinsky reaction

J. Li, 2009 .

Sharpless asymmetric amino-hydroxylation

J. Li, 2002 .