Combining Organocatalysis and Lanthanide Catalysis: A Sequential One-Pot Quadruple Reaction Sequence/Hetero-Diels-Alder Asymmetric Synthesis of Functionalized Tricycles

2016 ◽  
Vol 55 (52) ◽  
pp. 16153-16155 ◽  
Author(s):  
Simon Dochain ◽  
Fabrizio Vetica ◽  
Rakesh Puttreddy ◽  
Kari Rissanen ◽  
Dieter Enders
Keyword(s):  
Asymmetric Synthesis ◽  
Diels Alder ◽  
Reaction Sequence ◽  
One Pot

Combining Organocatalysis and Lanthanide Catalysis: A Sequential One-Pot Quadruple Reaction Sequence/Hetero-Diels-Alder Asymmetric Synthesis of Functionalized Tricycles

2016 ◽  
Vol 128 (52) ◽  
pp. 16387-16389 ◽  
Author(s):  
Simon Dochain ◽  
Fabrizio Vetica ◽  
Rakesh Puttreddy ◽  
Kari Rissanen ◽  
Dieter Enders
Keyword(s):  
Asymmetric Synthesis ◽  
Diels Alder ◽  
Reaction Sequence ◽  
One Pot

ChemInform Abstract: Multicatalytic Asymmetric Synthesis of Complex Tetrahydrocarbazoles via a Diels-Alder/Benzoin Reaction Sequence.

ChemInform ◽  
2012 ◽  
Vol 43 (27) ◽  
pp. no-no
Author(s):  
Yankai Liu ◽  
Manuel Nappi ◽  
Eduardo C. Escudero-Adan ◽  
Paolo Melchiorre
Keyword(s):  
Asymmetric Synthesis ◽  
Diels Alder ◽  
Reaction Sequence

An Efficient One-Pot Asymmetric Synthesis of Biaryl Compounds via Diels−Alder/Retro-Diels−Alder Cascade Reactions

2007 ◽  
Vol 9 (5) ◽  
pp. 805-808 ◽  
Author(s):  
Yongxiang Liu ◽  
Kui Lu ◽  
Mingji Dai ◽  
Kai Wang ◽  
Wanqing Wu ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Cascade Reactions ◽  
Diels Alder ◽  
One Pot ◽  
Biaryl Compounds

scholarly journals An Efficient One-Pot Asymmetric Synthesis of Biaryl Compounds via Diels—Alder/Retro-Diels—Alder Cascade Reactions.

ChemInform ◽  
2007 ◽  
Vol 38 (29) ◽  
Author(s):  
Yongxiang Liu ◽  
Kui Li ◽  
Mingji Dai ◽  
Kai Wang ◽  
Wanqing Wu ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Cascade Reactions ◽  
Diels Alder ◽  
One Pot ◽  
Biaryl Compounds

Entry into (E)-3-(1,2,4-oxadiazol-5-yl)acrylic acids via a one-pot ring-opening/ring-closing/retro-Diels-Alder reaction sequence

2020 ◽  
Vol 61 (9) ◽  
pp. 151543 ◽  
Author(s):  
Sofia Presnukhina ◽  
Marina Tarasenko ◽  
Sergey Baykov ◽  
Sergey N. Smirnov ◽  
Vadim P. Boyarskiy ◽  
...  
Keyword(s):  
Ring Opening ◽  
Alder Reaction ◽  
Diels Alder ◽  
Reaction Sequence ◽  
One Pot ◽  
Diels Alder Reaction ◽  
Acrylic Acids

Diastereoselective synthesis of functionalised carbazoles via a sequential Diels–Alder/ene reaction strategy

RSC Advances ◽  
2015 ◽  
Vol 5 (21) ◽  
pp. 16125-16152 ◽  
Author(s):  
Joseph Cowell ◽  
Matokah Abualnaja ◽  
Stephanie Morton ◽  
Ruth Linder ◽  
Faye Buckingham ◽  
...  
Keyword(s):  
Diels Alder ◽  
Diastereoselective Synthesis ◽  
Reaction Sequence ◽  
One Pot ◽  
Ene Reaction

A one-pot, three-component, synthesis of saturated carbazoles and related pyridazino[3,4-b]indoles is described, involving an intermolecular Diels–Alder/intermolecular ene reaction sequence with relative stereocontrol of up to four stereocentres.

The asymmetric synthesis of aryltetralin lignans: (−)-isolariciresinol dimethyl ether and (−)-deoxysikkimotoxin

1996 ◽  
Vol 74 (1) ◽  
pp. 88-94 ◽  
Author(s):  
Don M. Coltart ◽  
James L. Charlton
Keyword(s):  
Asymmetric Synthesis ◽  
Key Words ◽  
Dimethyl Ether ◽  
Selective Reduction ◽  
Diels Alder ◽  
Asymmetric Syntheses ◽  
One Pot ◽  
Synthetic Strategy

The total asymmetric syntheses of (−)-isolariciresinol dimethyl ether (6) and (−)-deoxysikkimotoxin (7) have been carried out, in an attempt to exploit a synthetic strategy recently developed for the synthesis of (−)-deoxypodophyllotoxin (1, R1 = -CH2−, Ar = 3,4,5-trimethoxyphenyl). In so doing, a generalized method for the synthesis of aryltetralin lignans has been developed that should be applicable to a variety of substitution patterns and stereochemistries. A one-pot, 100% regio-selective reduction–lactonization procedure has been developed for the conversion of the ester 18b to (−)-deoxysikkimotoxin, which gave 93% isolated yield in that step. Key words: ortho-quinodimethanes, lignans, Diels–Alder, asymmetric, mandelate.

Multicatalytic Asymmetric Synthesis of Complex Tetrahydrocarbazoles via a Diels–Alder/Benzoin Reaction Sequence

2012 ◽  
Vol 14 (5) ◽  
pp. 1310-1313 ◽  
Author(s):  
Yankai Liu ◽  
Manuel Nappi ◽  
Eduardo C. Escudero-Adán ◽  
Paolo Melchiorre
Keyword(s):  
Asymmetric Synthesis ◽  
Diels Alder ◽  
Reaction Sequence

One-pot, highly efficient, asymmetric synthesis of ring-fused piperidine derivatives bearing N,O- or N,N-acetal moieties

2016 ◽  
Vol 14 (8) ◽  
pp. 2444-2453 ◽  
Author(s):  
Ji-Yao Li ◽  
Zhi-Long Li ◽  
Wei-Wei Zhao ◽  
Yan-Kai Liu ◽  
Zhi-Ping Tong ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Alder Reaction ◽  
Diels Alder ◽  
One Pot ◽  
Highly Efficient ◽  
Diels Alder Reaction

Lactols or cyclic hemiaminals are directly used as nucleophiles in the asymmetric aza-Diels–Alder reaction to synthesize ring-fused piperidine derivatives.

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