Homogeneous catalysis: use of chiral titanocene complexes for asymmetric catalytic Diels–Alder reactions

William Odenkirk and B. Bosnich

J. Chem. Soc., Chem. Commun., 1995, 1181
DOI: 10.1039/C39950001181

Novel binaphthyl and biphenyl α- and β-amino acids and esters: organocatalysis of asymmetric Diels–Alder reactions. A combined synthetic and computational study

Philip C. Bulman Page, Francesca S. Kinsey, Yohan Chan, Ian R. Strutt, Alexandra M. Z. Slawin and Garth A. Jones

Org. Biomol. Chem., 2018, 16, 7400
DOI: 10.1039/C8OB01795F

Asymmetric induction in Diels‐Alder reactions to acrylates derived from chiral sec‐alcohols. Preliminary communication

Wolfgang Oppolzer, Mark Kurth, Daniel Reichlin, Christian Chapuis, Martin Mohnhaupt and Frank Moffatt

Helvetica Chimica Acta, 1981, 64, 2802
DOI: 10.1002/hlca.19810640841

Asymmetric Diels‐Alder Reactions of Cyclopentadiene with N‐Crotonoyl‐ and N‐Acryloyl‐4,4‐Dimethyl‐1,3‐Oxazolidin‐2‐one, Mediated by Chiral Lewis Acids

Christian Chapuis and Janusz Jurczak

Helvetica Chimica Acta, 1987, 70, 436
DOI: 10.1002/hlca.19870700223

Structural aspects and ring opening polymerization of ε-caprolactone using mono- and di-aluminum compounds incorporating bidentate pyrrole-morpholine ligands

Hung-Chang Hsiao, Amitabha Datta, Yun-Fan Chen, Weilun Chang, Ting-Yu Lee, Chia-Her Lin and Jui-Hsien Huang

Journal of Organometallic Chemistry, 2016, 804, 35
DOI: 10.1016/j.jorganchem.2015.12.030

Update 1 of: BINOL: A Versatile Chiral Reagent

Jean Michel Brunel

Chem. Rev., 2007, 107, PR1
DOI: 10.1021/cr078004a

2-Azabicyclo[2.2.1]hept-5-en-3-one: Chemical Profile of a Versatile Synthetic Building Block and its Impact on the Development of Therapeutics

Rohit Singh and Robert Vince

Chem. Rev., 2012, 112, 4642
DOI: 10.1021/cr2004822

Enantioselective synthesis of a conformationally rigid, sterically encumbered, 2-arsino-7-phosphanorbornene

Paul A Gugger, Anthony C Willis, S.Bruce Wild, Graham A Heath, Richard D Webster and John H Nelson

Journal of Organometallic Chemistry, 2002, 643-644, 136
DOI: 10.1016/S0022-328X(01)01209-8

Monomeric organoaluminium complexes RAl(OR*)2 and R2AlOR* with an optically active amino alkoxide ligand

T Gelbrich, E Hecht, K.-H Thiele and J Sieler

Journal of Organometallic Chemistry, 2000, 595, 21
DOI: 10.1016/S0022-328X(99)00516-1

An Application of Electronic Asymmetry to Highly Enantioselective Catalytic Diels−Alder Reactions

J. W. Faller, Brian J. Grimmond and Darlene G. D'Alliessi

J. Am. Chem. Soc., 2001, 123, 2525
DOI: 10.1021/ja003528c

α,β-Unsaturated oxazolines and oxazine, useful dienophiles in the Diels-Alder reaction

Annie Pouilhès, Cyrille Kouklovsky, Nicole Langlois and Yves Langlois

Tetrahedron Letters, 1987, 28, 6183
DOI: 10.1016/S0040-4039(00)61841-5

Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels–Alder Reaction

Xianxing Jiang and Rui Wang

Chem. Rev., 2013, 113, 5515
DOI: 10.1021/cr300436a

New Dienophiles: 1‐Acetylvinyl Arenecarboxylates. Reactivity toward cyclopentadiene and exocyclic dienes

Joaquin Tamariz and Pierre Vogel

Helvetica Chimica Acta, 1981, 64, 188
DOI: 10.1002/hlca.19810640121

Utility of Osmium(II) in the Catalysis of Asymmetric Diels−Alder Reactions

J. W. Faller and Jonathan Parr

Organometallics, 2001, 20, 697
DOI: 10.1021/om000896g

Enantioselective Synthesis of P-Chiral (η6-Arene)ruthenium(II) Complexes Using Enantiomerically Pure Orthometalated Palladium(II) Amine Complexes

Kesete Y. Ghebreyessus, Nizamettin Gül and John H. Nelson

Organometallics, 2003, 22, 2977
DOI: 10.1021/om030172f

Synthese und Charakterisierung chiraler Organogallium- und -aluminiumalkoholate mit intramolekularer Stickstoffstabilisierung. Röntgenstrukturanalyse von Dimethylgallium-(S)-2-dimethylamino-3-methyl-1-butanolat, Dimethylgallium-(S)-2-dimethylamino-3-phenyl-1-propanolat und Dimethylgallium-(R)-2-dimethylamino-1-butanolat

Herbert Schumann, Sonja Wernik, Birgit C. Wassermann and Frank Girgsdies

Journal of Organometallic Chemistry, 2001, 621, 317
DOI: 10.1016/S0022-328X(00)00767-1

Rare-Earth Metal Triflates in Organic Synthesis

Shū Kobayashi, Masaharu Sugiura, Hidetoshi Kitagawa and William W.-L. Lam

Chem. Rev., 2002, 102, 2227
DOI: 10.1021/cr010289i

Asymmetrische Induktion bei Diels‐Alder‐Reaktionen

Nachr. Chem. Tech. Lab., 1987, 35, 836
DOI: 10.1002/nadc.19870350807

A highly enantioselective [4+2] cycloaddition involving aldehydes and β,γ-unsaturated-α-keto esters

Nanda Kumar Katakam, Yejin Kim and Allan D. Headley

Tetrahedron: Asymmetry, 2017, 28, 1591
DOI: 10.1016/j.tetasy.2017.09.019

A New Chiral at Metal Catalyst for Enantioselective Diels−Alder Reactions: Observation of Isomeric Intermediates

J. W. Faller and Brian J. Grimmond

Organometallics, 2001, 20, 2454
DOI: 10.1021/om0010767

Enantioselective [4+2] Cycloaddition of Buta‐1,3‐dienes to Alkyl Glyoxylates Catalyzed by the Chiral (Salen)Chromium(III) Complex

Piotr Kwiatkowski, Monika Asztemborska, Jean‐Claude Caille and Janusz Jurczak

Adv Synth Catal, 2003, 345, 506
DOI: 10.1002/adsc.200390058

Aluminum Compounds Containing Pyrrole–Imine Ligand Systems – Synthesis, Characterization, Structure Elucidation, Ring‐Opening Polymerization, and Catalytic Meerwein–Ponndorf–Verley Reaction

Shu‐Ya Hsu, Ching‐Han Hu, Cheng‐Yi Tu, Chia‐Her Lin, Ren‐Yung Chen, Amitabha Datta and Jui‐Hsien Huang

Eur J Inorg Chem, 2014, 2014, 1965
DOI: 10.1002/ejic.201400082

Organocatalysis using protonated 1,2-diamino-1,2-diphenylethane for asymmetric Diels–Alder reaction

Kyoung Hoon Kim, Seil Lee, Dae-Woong Lee, Dong-Hyun Ko and Deok-Chan Ha

Tetrahedron Letters, 2005, 46, 5991
DOI: 10.1016/j.tetlet.2005.07.025

Recent advances in homogeneous enantioselective Diels–Alder reactions catalyzed by chiral transition-metal complexes

Daniel Carmona, M Pilar Lamata and Luis A Oro

Coordination Chemistry Reviews, 2000, 200-202, 717
DOI: 10.1016/S0010-8545(00)00355-6

ChemInform Abstract: ASYMMETRIC DIELS‐ALDER REACTION CATALYZED BY CHIRAL ALKOXYALUMINUM DICHLORIDE

S. HASHIMOTO, N. KOMESHIMA and K. KOGA

Chemischer Informationsdienst, 1979, 10
DOI: 10.1002/chin.197946095

Modifizierte Isopinocampheyldibromborane; selektive Katalysatoren für asymmetrische Diels-Alder-rekationen

Gerhard Bir and Dieter Kaufmann

Journal of Organometallic Chemistry, 1990, 390, 1
DOI: 10.1016/0022-328X(90)85075-A

Aluminium annual survey for the year 1979

J. David Smith

Journal of Organometallic Chemistry, 1981, 207, 67
DOI: 10.1016/S0022-328X(00)88924-X

Asymmetrische Diels‐Alder‐Reaktionen

Peter Welzel

Nachr. Chem. Tech. Lab., 1983, 31, 979
DOI: 10.1002/nadc.19830311211

Electronic and steric factors affecting the formation of four or five-coordinated aluminum complexes: syntheses and crystal structures of some aluminum alkoxides

Chia-Her Lin, Bao-Tsan Ko, Fa-Cherng Wang, Chu-Chieh Lin and Chen-Yuan Kuo

Journal of Organometallic Chemistry, 1999, 575, 67
DOI: 10.1016/S0022-328X(98)00968-1

The application of the formyl CH--O hydrogen bond postulate to the understanding of enantioselective reactions involving chiral boron lewis acids and aldehydes

E.J. Corey and Jeffrey J. Rohde

Tetrahedron Letters, 1997, 38, 37
DOI: 10.1016/S0040-4039(96)02249-6

Chiral lewis acids supported on silica gel and alumina, and their use as catalysts in Diels-Alder reactions of methacrolein and bromoacrolein

JoséM Fraile, JoséI García, JoséA Mayoral and Ana J Royo

Tetrahedron: Asymmetry, 1996, 7, 2263
DOI: 10.1016/0957-4166(96)00281-9

Complete asymmetric inductions in diels-alder reactions of chiral sulfines

Pascal A.T.W. Porskamp, R. Curtis Haltiwanger and Binne Zwanenburg

Tetrahedron Letters, 1983, 24, 2035
DOI: 10.1016/S0040-4039(00)81837-7

d-Isomannide in synthesis: asymmetric Diels–Alder reactions with novel homochiral bis-imine Cu2+-catalysts

Gert De Coster, Koen Vandyck, Erik Van der Eycken, Johan Van der Eycken, Myriam Elseviers and Harald Röper

Tetrahedron: Asymmetry, 2002, 13, 1673
DOI: 10.1016/S0957-4166(02)00411-1

Excavations in drug chirality: 1. Cyclothiazide

Elfriede Nusser, Anirban Banerjee and Joseph Gal

Chirality, 1991, 3, 2
DOI: 10.1002/chir.530030103

Recent advances in asymmetric synthesis-II

J.W. ApSimon and T. Lee Collier

Tetrahedron, 1986, 42, 5157
DOI: 10.1016/S0040-4020(01)82073-1

Lanthanide trifluoromethanesulfonates as reusable catalysts. Michael and Diels-Alder reactions

Shū Kobayashi, Iwao Hachiya, Takeshi Takahori, Mitsuharu Araki and Haruro Ishitani

Tetrahedron Letters, 1992, 33, 6815
DOI: 10.1016/S0040-4039(00)61783-5

Asymmetric Diels-Alder reaction catalyzed by a chiral ytterbium trifluoromethanesulfonate

Shū Kobayashi, Iwao Hachiya, Haruro Ishitani and Mitsuharu Araki

Tetrahedron Letters, 1993, 34, 4535
DOI: 10.1016/0040-4039(93)88078-W

Chirale Lewis‐Säuren

Nachr. Chem. Tech. Lab., 1988, 36, 906
DOI: 10.1002/nadc.19880360808

Evidence for the importance of π-π-attractive interactions in Enantioselective Diels-Alder reactions chiral catalysts of type (RO)2TiCl2

E.J. Corey and Yasushi Matsumura

Tetrahedron Letters, 1991, 32, 6289
DOI: 10.1016/0040-4039(91)80149-Z

Enantiomerically pure α-pinene derivatives from material of 65% enantiomeric purity. Part 1: Di[3α-(2α-hydroxy)pinane]amine

Stanisław W. Markowicz, Katarzyna Pokrzeptowicz, Janina Karolak-Wojciechowska, Robert Czylkowski, Jan Omelańczuk and Agata Sobczak

Tetrahedron: Asymmetry, 2002, 13, 1981
DOI: 10.1016/S0957-4166(02)00512-8

Three-Component Synthesis of Substituted Perhydropyrans from β-Styrylmalonates, Aldehydes, and Alkoxyaluminum Dichlorides

Denis D. Borisov, Roman A. Novikov and Yury V. Tomilov

Org. Lett., 2024, 26, 1022
DOI: 10.1021/acs.orglett.3c04097

A reinvestigation of asymmetric induction in diels-alder reactions to chiral acrylates.

Wolfgang Oppolzer, Mark Kurth, Daniel Reichlin and Frank Moffatt

Tetrahedron Letters, 1981, 22, 2545
DOI: 10.1016/S0040-4039(01)90516-7

Design and Stereoselective Preparation of a New Class of Chiral Olefin Metathesis Catalysts and Application to Enantioselective Synthesis of Quebrachamine: Catalyst Development Inspired by Natural Product Synthesis

Elizabeth S. Sattely, Simon J. Meek, Steven J. Malcolmson, Richard R. Schrock and Amir H. Hoveyda

J. Am. Chem. Soc., 2009, 131, 943
DOI: 10.1021/ja8084934

Asymmetric Catalysis with Heterobimetallic Compounds

Masakatsu Shibasaki, Hiroaki Sasai and Takayoshi Arai

Angew. Chem. Int. Ed. Engl., 1997, 36, 1236
DOI: 10.1002/anie.199712361

Complete Characterization of a Chiral Lewis Acid−Product Complex for the Enantioselective Diels−Alder Reaction between Methacrolein and Cyclopentadiene: Mechanistic Considerations

Daniel Carmona, M. Pilar Lamata, Fernando Viguri, Ricardo Rodríguez, Carmen Barba, Fernando J. Lahoz, M. Luisa Martín, Luis A. Oro and Luis Salvatella

Organometallics, 2007, 26, 6493
DOI: 10.1021/om700717e

Studies on the Asymmetric Diels-Alder Reaction of Dihydropyridin-2-one with Silyloxydienes

Atsushi Nishida, Masamichi Yamanaka, Toshiaki Nagata, Yoshino Nakajima and Masako Nakagawa

HETEROCYCLES, 2002, 56, 283
DOI: 10.3987/COM-01-S(K)37

Asymmetric Diels–Alder reaction with >C=P– functionality of the 2-phosphaindolizine-η1-P-aluminium(O-menthoxy) dichloride complex: experimental and theoretical results

Rajendra K Jangid, Nidhi Sogani, Neelima Gupta, Raj Kumar Bansal, Moritz von Hopffgarten and Gernot Frenking

Beilstein J. Org. Chem., 2013, 9, 392
DOI: 10.3762/bjoc.9.40

Asymmetric Diels-Alder reactions catalyzed by chiral lanthanide(III) trifluoromethanesulfonates. Unique structure of the triflate and stereoselective synthesis of both enantiomers using a single chiral source and a choice of achiral ligands

Shū Kobayashi, Haruro Ishitani, Iwao Hachiya and Mitsuharu Araki

Tetrahedron, 1994, 50, 11623
DOI: 10.1016/S0040-4020(01)85657-X

Positive Cooperativity of Product Mimics in the Asymmetric Autoinduction of Diels−Alder Reactions Catalyzed by a VAPOL−Aluminum Catalyst

Douglas P. Heller, Daniel R. Goldberg and William D. Wulff

J. Am. Chem. Soc., 1997, 119, 10551
DOI: 10.1021/ja971246f

Chirale Alkoxytitan(IV)‐Komplexe für enantioselektive nucleophile Additionen an Aldehyde und als Lewis‐Säuren in Diels‐Alder‐Reaktionen

Dieter Seebach, Albert K. Beck, René Imwinkelzied, Silvio Roggo and Anne Wonnacott

Helvetica Chimica Acta, 1987, 70, 954
DOI: 10.1002/hlca.19870700406

Natural products as inspiration for the development of asymmetric catalysis

Justin T. Mohr, Michael R. Krout and Brian M. Stoltz

Nature, 2008, 455, 323
DOI: 10.1038/nature07370

Asymmetric Diels–Alder reactions of 2-fluoroacrylic acid derivatives. Part 2: A remarkable effect of fluorine substituent on the diastereoselectivity

Hisanaka Ito, Akio Saito and Takeo Taguchi

Tetrahedron: Asymmetry, 1998, 9, 1989
DOI: 10.1016/S0957-4166(98)00196-7

Investigation of a chiral masked ketene synthon synthesis of the (+)-(1r4r) and (−)-1s,4s) enantiomers of dehydronorcamphor

Christian Maignan and Ralph A Raphael

Tetrahedron, 1983, 39, 3245
DOI: 10.1016/S0040-4020(01)91570-4

Asymmetrische Diels‐Alder‐ und En‐Reaktionen in der Organischen Synthese

Wolfgang Oppolzer

Angewandte Chemie, 1984, 96, 840
DOI: 10.1002/ange.19840961105

Lewis Base Activation of Lewis Acids: Catalytic Enantioselective Allylation and Propargylation of Aldehydes

Scott E. Denmark and Thomas Wynn

J. Am. Chem. Soc., 2001, 123, 6199
DOI: 10.1021/ja016017e

Asymmetric base-catalyzed cycloaddition between anthrone and some dienophiles

Olivier Riant, Henri B. Kagan and Louis Ricard

Tetrahedron, 1994, 50, 4543
DOI: 10.1016/S0040-4020(01)89385-6

Ruthenium–Lewis Acid Catalyzed Asymmetric Diels–Alder Reactions between Dienes and α,β‐Unsaturated Ketones

Jenny Rickerby, Martial Vallet, Gerald Bernardinelli, Florian Viton and E. Peter Kündig

Chemistry A European J, 2007, 13, 3354
DOI: 10.1002/chem.200600851

Synthesis of polymer-supported chiral N-sulfonylamino acids and their use in asymmetric diels-alder reaction of cyclopentadiene with methacrolein

Koichi Kamahori, Shoichi Tada, Koichi Ito and Shinichi Itsuno

Tetrahedron: Asymmetry, 1995, 6, 2547
DOI: 10.1016/0957-4166(95)00333-K

Intramolecular CH⋯O hydrogen bond controlling the conformation of heterocycles: synthesis, structure and catalytic reactivity of aluminum aryloxides

Chia-Her Lin, Liang-Fu Yan, Fa-Cherng Wang, Yih-Lu Sun and Chu-Chieh Lin

Journal of Organometallic Chemistry, 1999, 587, 151
DOI: 10.1016/S0022-328X(99)00268-5

Lewis Base Adducts Derived from Transfer Hydrogenation Catalysts: Scope and Selectivity

Zachariah M. Heiden, Bradford J. Gorecki and Thomas B. Rauchfuss

Organometallics, 2008, 27, 1542
DOI: 10.1021/om700996m

Synthesis and Application of Chiral 2-Amido and 1-Phenyl-2-amido Dienes in Diels–Alder Reactions to Access Chiral Cyclic Ketones

Aoibheann O’ Connor, Calvin Q. O’Broin, Julia Bruno-Colmenarez and Patrick J. Guiry

J. Org. Chem., 2024, 89, 16325
DOI: 10.1021/acs.joc.4c00689

Asymmetric Diels-Alder reaction of cyclopentadiene with methacrolein using polymer-supported chiral catalysts

Shinichi Itsuno, Katsuhiro Watanabe, Takahiro Koizumi and Koichi Ito

Reactive Polymers, 1995, 24, 219
DOI: 10.1016/0923-1137(94)00087-L

Enantioselective catalysis using planar chiral η6-arene chromium complexes: 1,2-diols as cycloaddition catalysts

Graham B Jones, Mustafa Guzel and Steven B Heaton

Tetrahedron: Asymmetry, 2000, 11, 4303
DOI: 10.1016/S0957-4166(00)00411-0

The synthesis of carbohydrate derivatives from acyclic precursors

David J. Ager and Michael B. East

Tetrahedron, 1993, 49, 5683
DOI: 10.1016/S0040-4020(01)87942-4

Asymmetric Diels−Alder Reaction of Methacrolein with Cyclopentadiene Using Polymer-Supported Catalysts: Design of Highly Enantioselective Polymeric Catalysts

Koichi Kamahori, Koichi Ito and Shinichi Itsuno

J. Org. Chem., 1996, 61, 8321
DOI: 10.1021/jo960518e

Defining the Conformation of Lewis Acid/Lewis Base Complex: Crystallographic Evidence for Simultaneous σ and π Donation by a Carbonyl Group to a Divalent Boron Lewis Acid

Michael C. Amendola, Kenneth E. Stockman, Diego A. Hoic, William M. Davis and Gregory C. Fu

Angew. Chem. Int. Ed. Engl., 1997, 36, 267
DOI: 10.1002/anie.199702671

Highly enantioselective Diels–Alder catalysis with a chiral ruthenium bisoxazoline complex

J.W Faller and Adrien Lavoie

Journal of Organometallic Chemistry, 2001, 630, 17
DOI: 10.1016/S0022-328X(01)00871-3

Asymmetric Diels-Alder reaction catalysed by some chiral Lewis acids

F. Rebiere, O. Riant and H.B. Kagan

Tetrahedron: Asymmetry, 1990, 1, 199
DOI: 10.1016/0957-4166(90)90014-2

Effects of torsional angles of 2,2′-biaryldiol ligands in asymmetric Diels-Alder reactions of acrylates catalyzed by their titanium complexes

Toshiro Harada, Masahiro Takeuchi, Masanori Hatsuda, Shinji Ueda and Akira Oku

Tetrahedron: Asymmetry, 1996, 7, 2479
DOI: 10.1016/0957-4166(96)00311-4

The structure of the 2-methylacrolein boron trifluoride complex in the crystalline phase and in solution

E.J. Corey, Teck-Peng Loh, Sepehr Sarshar and Mihai Azimioara

Tetrahedron Letters, 1992, 33, 6945
DOI: 10.1016/S0040-4039(00)60902-4

Oxazaborolidine‐Derived Lewis Acid Assisted Lewis Acid as a Moisture‐Tolerant Catalyst for Enantioselective Diels–Alder Reactions

Kentaro Futatsugi and Hisashi Yamamoto

Angew Chem Int Ed, 2005, 44, 1484
DOI: 10.1002/anie.200461319

ASYMMETRIC ALLYLATION OF ALDEHYDES WITH ETHERIFICATION BY ALLYLTRIMETHYLSILANE PROMOTED BY CHIRAL ALCOHOL MODIFIED ALUMINUM REAGENTS

Yang Yang and Dong Wang

Phosphorus, Sulfur, and Silicon and the Related Elements, 1998, 139, 193
DOI: 10.1080/10426509808035688

Chirality in Organic and Mineral Systems: A Review of Reactivity and Alteration Processes Relevant to Prebiotic Chemistry and Life Detection Missions

Carina Lee, Jessica Weber, Laura Rodriguez, Rachel Sheppard, Laura Barge, Eve Berger and Aaron Burton

Symmetry, 2022, 14, 460
DOI: 10.3390/sym14030460

Diastereoselectivity an chiral ruthenium complexes of chiraphos monoxide ligands: Epimerization, quasiracemates, and lewis acid catalysis

J.W. Faller, Xiang Liu and Jonathan Parr

Chirality, 2000, 12, 325
DOI: 10.1002/(SICI)1520-636X(2000)12:5/6<325::AID-CHIR5>3.0.CO;2-6

New homochiral ketoalcohols from aldol reactions of (+)-isomenthone and reversal of diastereoselectivity

Jameel H. Chughtai, John M. Gardiner, Steven G. Harris, Simon Parsons, David W.H. Rankin and Carl H. Schwalbe

Tetrahedron Letters, 1997, 38, 9043
DOI: 10.1016/S0040-4039(97)10430-0

BINOL: A Versatile Chiral Reagent

Jean Michel Brunel

Chem. Rev., 2005, 105, 857
DOI: 10.1021/cr040079g

Highly efficient molybdenum-based catalysts for enantioselective alkene metathesis

Steven J. Malcolmson, Simon J. Meek, Elizabeth S. Sattely, Richard R. Schrock and Amir H. Hoveyda

Nature, 2008, 456, 933
DOI: 10.1038/nature07594

Can a chiral catalyst containing the same ligand/metal components promote the formation of both enantiomers enantioselectively? The bis(oxazoline)-magnesium perchlorate-catalyzed asymmetric Diels-Alder reaction

Giovanni Desimoni, Giuseppe Faita, Anna Gamba Invernizzi and Pierpaolo Righetti

Tetrahedron, 1997, 53, 7671
DOI: 10.1016/S0040-4020(97)00433-X

Catalytic Enantioselective Diels Alder Reaction: Application in the Synthesis of Antiviral Agents

Alessandro Grillo and Bruno Mattia Bizzarri

Catalysts, 2022, 12, 150
DOI: 10.3390/catal12020150

Asymmetric diels-alder reactions catalyzed by chiral oxazaborolidines. Effect of the position of an electron-donor functionality in the α-side chain substituent on the enantioselectivity

Jean-Paul G. Seerden and Hans W. Scheeren

Tetrahedron Letters, 1993, 34, 2669
DOI: 10.1016/S0040-4039(00)77652-0

Asymmetric cycloaddition routes to both enantiomers of trans-9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboxylic acid

Linda Thunberg and Stig Allenmark

Tetrahedron: Asymmetry, 2003, 14, 1317
DOI: 10.1016/S0957-4166(03)00172-1

Diels–Alder reaction of 2-phosphaindolizines catalysed by organoaluminium reagent: theoretical and experimental results

Rajendra K. Jangid, Neelima Gupta, Raj K. Bansal, Moritz von Hopffgarten and Gernot Frenking

Tetrahedron Letters, 2011, 52, 1721
DOI: 10.1016/j.tetlet.2011.02.007

Complexes containing a Lewis acid and Brønsted acid for the catalytic asymmetric Diels-Alder reaction

Varinder K. Aggarwal, Emma Anderson, Robert Giles and Anne Zaparucha

Tetrahedron: Asymmetry, 1995, 6, 1301
DOI: 10.1016/0957-4166(95)00163-J

New L-Serine Derivative Ligands as Cocatalysts for Diels-Alder Reaction

Carlos A. D. Sousa, José E. Rodríguez-Borges and Cristina Freire

ISRN Organic Chemistry, 2013, 2013, 1
DOI: 10.1155/2013/217675

Design of Brønsted Acid-Assisted Chiral Lewis Acid (BLA) Catalysts for Highly Enantioselective Diels−Alder Reactions

Kazuaki Ishihara, Hideki Kurihara, Masayuki Matsumoto and Hisashi Yamamoto

J. Am. Chem. Soc., 1998, 120, 6920
DOI: 10.1021/ja9810282

Optically Active Polymer Synthesis by Diels−Alder Polymerization with Chirally Modified Lewis Acid Catalyst

Koichi Kamahori, Shoichi Tada, Koichi Ito and Shinichi Itsuno

Macromolecules, 1999, 32, 541
DOI: 10.1021/ma9815410

New Lewis acid catalysts for the Diels-Alder reaction

T. Ross Kelly, Sanat K. Maity, Premji Meghani and Nizal S. Chandrakumar

Tetrahedron Letters, 1989, 30, 1357
DOI: 10.1016/S0040-4039(00)99464-4

Festlegung der Konformation von Lewis‐Säure‐Base‐Komplexen: kristallographischer Beweis gleichzeitiger σ‐ und π‐Koordination einer Carbonylgruppe an eine Lewis‐Säure mit zweiwertigem Bor

Michael C. Amendola, Kenneth E. Stockman, Diego A. Hoic, William M. Davis and Gregory C. Fu

Angewandte Chemie, 1997, 109, 278
DOI: 10.1002/ange.19971090325

Enzymatic intermolecular Diels-Alder reactions in synthesis: From nature to design

Lei Gao, Jun Yang and Xiaoguang Lei

Tetrahedron Chem, 2022, 2, 100013
DOI: 10.1016/j.tchem.2022.100013

Asymmetric Diels-Alder reaction catalyzed by chiral bases

Olivier Riant and Henri B. Kagan

Tetrahedron Letters, 1989, 30, 7403
DOI: 10.1016/S0040-4039(00)70709-X

Asymmetric Diels-Alder reactions of cyclopentadiene in the synthesis of chiral norbornene derivatives

E. G. Mamedov and E. I. Klabunovskii

Russ J Org Chem, 2008, 44, 1097
DOI: 10.1134/S1070428008080010

REAGENT-CONTROLLED ASYMMETRIC DIELS-ALDER REACTIONS. A REVIEW

Taeboem Oh and Michael Rally

Organic Preparations and Procedures International, 1994, 26, 129
DOI: 10.1080/00304949409458024

C2-Symmetric bis-sulfoxides as chiral ligands in metal catalysed asymmetric diels-alder reactions.

Noureddine Khiar, Inmaculada Fernández and Felipe Alcudia

Tetrahedron Letters, 1993, 34, 123
DOI: 10.1016/S0040-4039(00)60073-4

Oxazaborolidine‐Derived Lewis Acid Assisted Lewis Acid as a Moisture‐Tolerant Catalyst for Enantioselective Diels–Alder Reactions

Kentaro Futatsugi and Hisashi Yamamoto

Angewandte Chemie, 2005, 117, 1508
DOI: 10.1002/ange.200461319

High asymmetric induction in diels-alder additions of cyclopentadiene to acrylates derived from isoborneol

Wolfgang Oppolzer, Christian Chapuis, Guo Mao Dao, Daniel Reichlin and Thierry Godel

Tetrahedron Letters, 1982, 23, 4781
DOI: 10.1016/S0040-4039(00)85712-3

1‐Aminoindan‐2‐ol, a Suitable Ligand for the Synthesis of Chiral, Intramolecularly Stabilized Compounds of Aluminum, Gallium, and Indium

Herbert Schumann, Jens Kaufmann and Sebastian Dechert

Zeitschrift anorg allge chemie, 2004, 630, 1999
DOI: 10.1002/zaac.200400236

Synthesis and characterization of aluminum ethyl-(S)-lactate complexes and VT NMR studies of [Bu2iAl((S)-(−)-μ2-OC(H)(Me)C(O)OEt))]2

Bao-Tsan Ko, Fa-Cherng Wang, Yih-Lu Sun, Chia-Her Lin, Chu-Chieh Lin and Chen-Yuan Kuo

Polyhedron, 1998, 17, 4257
DOI: 10.1016/S0277-5387(98)00236-8