Koichi Fujiwara, Hirokazu Tsukamoto, Miho Izumikawa, Takahiro Hosoya, Noritaka Kagaya, Motoki Takagi, Hideki Yamamura, Masayuki Hayakawa, Kazuo Shin-ya and Takayuki Doi

J. Org. Chem., 2015, 80, 114
DOI: 10.1021/jo502198y

The reaction of the Baylis-Hillman adducts of N-tosylimines with N,N-dimethylformamide dimethylacetal

Hong Jung Lee, Hyoung Shik Kim and Jae Nyoung Kim

Tetrahedron Letters, 1999, 40, 4363
DOI: 10.1016/S0040-4039(99)00749-2

Recent Contributions from the Baylis−Hillman Reaction to Organic Chemistry

Deevi Basavaiah, Bhavanam Sekhara Reddy and Satpal Singh Badsara

Chem. Rev., 2010, 110, 5447
DOI: 10.1021/cr900291g

Diastereoselective 1,3-dipolar intramolecular nitrone olefin cycloaddition (INOC) reaction of a sugar-derived allyl alcohol: Synthesis of functionalized aminocyclopentitols

Rajendra Rohokale

Carbohydrate Research, 2024, 543, 109223
DOI: 10.1016/j.carres.2024.109223

Synthesis of stereochemically defined (E)-cinnamyl alcohol derivatives from the Baylis–Hillman adducts

Hyoung Shik Kim, Tae Yi Kim, Ka Young Lee, Yun Mi Chung, Hong Jung Lee and Jae Nyoung Kim

Tetrahedron Letters, 2000, 41, 2613
DOI: 10.1016/S0040-4039(00)00229-X

A Novel and Facile Synthesis of Functionalized [4.4.3] and [4.4.4]Propellano-bislactones Using Acetates of the Baylis−Hillman Adducts

Deevi Basavaiah and Tummanapalli Satyanarayana

Org. Lett., 2001, 3, 3619
DOI: 10.1021/ol016469w

Solid-State Melt Reaction for the Domino Process: Highly Efficient Synthesis of Fused Tetracyclic Chromenopyran Pyrimidinediones Using Baylis−Hillman Derivatives

Manickam Bakthadoss, Govindan Sivakumar and Damodharan Kannan

Org. Lett., 2009, 11, 4466
DOI: 10.1021/ol901228j

ChemInform Abstract: Applications of Baylis‐Hillman Coupling Products: A Remarkable Reversal of Stereochemistry from Esters to Nitriles: A Simple Synthesis of (2E)‐2‐Methylalk‐2‐en‐1‐ols and (2Z)‐2‐Methylalk‐2‐ enenitriles.

D. BASAVAIAH and P. K. S. SARMA

ChemInform, 1992, 23
DOI: 10.1002/chin.199243108

Synthesis of 3-substituted-4-hydroxyquinoline N-oxides from the Baylis–Hillman adducts of o-nitrobenzaldehydes

Ka Young Lee, Jeong Mi Kim and Jae Nyoung Kim

Tetrahedron, 2003, 59, 385
DOI: 10.1016/S0040-4020(02)01518-1

Nucleophilic addition of triethyl phosphite to acetates of the baylis-hillman adducts: Stereoselective synthesis of (E)- and (Z)-allylphosphonates

Deevi Basavaiah and Subramanian Pandiaraju

Tetrahedron, 1996, 52, 2261
DOI: 10.1016/0040-4020(95)01055-6

NOVEL TITANIUM(IV) CHLORIDE CATALYZED OLEFINATION OF ALDEHYDES: A SIMPLE AND CONVENIENT SYNTHESIS OFTRANS-CINNAMIC ACIDS

Deevi Basavaiah and Anumolu Jaganmohan Rao

Synthetic Communications, 2002, 32, 195
DOI: 10.1081/SCC-120002002

Highly Stereoselective Synthesis of Tricyclic Chromenoisoxazolidines by Intramolecular 1,3‐Dipolar Cycloadditions

Manickam Bakthadoss and Gandhi Murugan

Eur J Org Chem, 2010, 2010, 5825
DOI: 10.1002/ejoc.201000804

The Baylis-Hillman reaction: A novel carbon-carbon bond forming reaction

Deevi Basavaiah, Polisetti Dharma Rao and Rachakonda Suguna Hyma

Tetrahedron, 1996, 52, 8001
DOI: 10.1016/0040-4020(96)00154-8

Synthetic Organic Chemistry with 2-Ethoxy-2-(phenylselenenyl)perfluoroalk-2-enenitrile: Application to α-Cyanoperfluoroacylation of Aldehydes

Mitsuhiro Yoshimatsu and Yoshie Timura

J. Org. Chem., 2002, 67, 5678
DOI: 10.1021/jo0201880

Synthesis of 3-quinolinecarboxylic acid esters from the Baylis–Hillman adducts of 2-halobenzaldehyde N-tosylimines

Jae Nyoung Kim, Hong Jung Lee, Ka Young Lee and Hyoung Shik Kim

Tetrahedron Letters, 2001, 42, 3737
DOI: 10.1016/S0040-4039(01)00552-4

Baylis–Hillman Bromides as a Source of 1,3‐Dipoles: Sterically Directed Synthesis of Oxindole‐Fused Spirooxirane and Spirodihydrofuran Frameworks

Deevi Basavaiah, Satpal Singh Badsara and Bharat Chandra Sahu

Chemistry A European J, 2013, 19, 2961
DOI: 10.1002/chem.201203756

Applications of Baylis–Hillman acetates: one-pot, facile and convenient synthesis of substituted γ-lactams

Deevi Basavaiah and Jamjanam Srivardhana Rao

Tetrahedron Letters, 2004, 45, 1621
DOI: 10.1016/j.tetlet.2003.12.133

Quinolines from Morita–Baylis–Hillman acetates of 2-azidobenzaldehydes

Eun-Gu Han, Hea Jung Kim and Kee-Jung Lee

Tetrahedron, 2009, 65, 9616
DOI: 10.1016/j.tet.2009.09.047

Preparation of Multifunctional Stereodefined Dienes

Fanie R. van Heerden, Johan J. Huyser and Cedric W. Holzapfel

Synthetic Communications, 1994, 24, 2863
DOI: 10.1080/00397919408010606

A highly regio- and stereoselective Pd-catalyzed tandem allylic rearrangement/intramolecular decarboxylative coupling of aryl propiolates derived from Baylis–Hillman adducts

Tummanapalli Satyanarayana, Dhanunjaya Naidu Vangapandu, Parthasarathy Muthuraman and Shashidhar Nizalapur

Tetrahedron Letters, 2015, 56, 2008
DOI: 10.1016/j.tetlet.2015.02.125

Recent Advances in the Baylis−Hillman Reaction and Applications

Deevi Basavaiah, Anumolu Jaganmohan Rao and Tummanapalli Satyanarayana

Chem. Rev., 2003, 103, 811
DOI: 10.1021/cr010043d

Preparation of N-protected allylic amines and α-methylene-β-amino acids from vinylalumination/Baylis–Hillman products via tandem SN2′ substitution–Overman rearrangement

P. Veeraraghavan Ramachandran, Thomas E. Burghardt and M. Venkat Ram Reddy

Tetrahedron Letters, 2005, 46, 2121
DOI: 10.1016/j.tetlet.2005.01.110

Synthesis of 3-Ethoxycarbonyl-4-hydroxyquinoline N-Oxides from the Baylis−Hillman Adducts of o-Nitrobenzaldehydes

Jae Nyoung Kim, Ka Young Lee, Hyoung Shik Kim and Tae Yi Kim

Org. Lett., 2000, 2, 343
DOI: 10.1021/ol9903741

Metallic samarium and iodine promoted facile and efficient syntheses of trisubstituted alkenes from the acetates of Baylis–Hillman adducts

Jian Li, Hua Xu and Yongmin Zhang

Tetrahedron Letters, 2005, 46, 1931
DOI: 10.1016/j.tetlet.2005.01.136

Reaction of a Cyclic Oxosulfonium Ylide with Acetates of the Baylis-Hillman Adducts: Tandem Michael−Intramolecular Corey-Chaykovsky Reactions

Hitoshi Akiyama, Tetsuya Fujimoto, Katsuyoshi Ohshima, Kenji Hoshino, Iwao Yamamoto and Ryozo Iriye

Org. Lett., 1999, 1, 427
DOI: 10.1021/ol990069f

APPLICATION OF TMSOTf IN THE BAYLIS-HILLMAN ADDUCTS

Subramanian Ravichandran

Synthetic Communications, 2001, 31, 2345
DOI: 10.1081/SCC-100104835

Simple, One‐Pot, and Facile Synthesis of Angularly Fused [6‐7‐5], [6‐7‐6], [6‐7‐7], and [6,7] Ring Systems Using Baylis–Hillman Acetates

Deevi Basavaiah, Kunche Aravindu, Katta Santosh Kumar and Kanumuri Ramesh Reddy

Eur J Org Chem, 2010, 2010, 1843
DOI: 10.1002/ejoc.200901483

Hydroxy-assisted catalyst-free Michael addition-dehydroxylation of Baylis–Hillman adducts in poly(ethylene glycol)

S. Chandrasekhar, B. Saritha, V. Jagadeshwar, Ch. Narsihmulu, Dolly Vijay, G. Dattatreya Sarma and B. Jagadeesh

Tetrahedron Letters, 2006, 47, 2981
DOI: 10.1016/j.tetlet.2006.02.104

Stereospecific Formation of Optically Active 5-Alkyl-4-methyl-3-[(trialkylsilyl)oxy]-2-([(trialkylsilyl)oxy]- methyl)tetrahydrofurans via Diastereoselective Epoxidation and Rearrangement of 5-[(Trialkylsilyl)oxy]-2-alken-1-ols1

Michael E. Jung and Derin C. D'Amico

J. Am. Chem. Soc., 1997, 119, 12150
DOI: 10.1021/ja972507o

Synthesis of trisubstituted alkenes by reductive dehydroxylation of Baylis–Hillman adducts using polymethylhydrosiloxane (PMHS) and catalytic B(C6F5)3

S. Chandrasekhar, G. Chandrashekar, K. Vijeender and M. Srinivasa Reddy

Tetrahedron Letters, 2006, 47, 3475
DOI: 10.1016/j.tetlet.2006.03.014

Crystal Structure of N-(2-Cyano-1-Phenylprop-2-en-1-yl)-4-Methylbenzenesulfonamide

R. A. C. Souza, S. Guilardi, M. M. M. Rubinger, L. R. Terra, E. C. Tavares and J. A. Ellena

J Struct Chem, 2018, 59, 1192
DOI: 10.1134/S0022476618050244

The Johnson-Claisen rearrangement of 3-hydroxy-2-methylenealkanenitriles: Stereoselective synthesis of functionalized trisubstituted alkenes

Deevi Basavaiah and Subramanian Pandiaraju

Tetrahedron Letters, 1995, 36, 757
DOI: 10.1016/0040-4039(94)02360-N