Stereoselective synthesis of (3R,3aS,7aS*)-3-aryloctahydroindol-2-ones using radical cyclisation: a formal synthesis of (±)-pancracine

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/a900467j ◽

1999 ◽

pp. 1949-1956 ◽

Cited By ~ 25

Author(s):

Masazumi Ikeda ◽

Masahiro Hamada ◽

Takashi Yamashita ◽

Katsuaki Matsui ◽

Tatsunori Sato ◽

...

Keyword(s):

Stereoselective Synthesis ◽

Formal Synthesis

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ChemInform Abstract: Stereoselective Synthesis of Petrosterol and a Formal Synthesis of Aragusterols.

ChemInform ◽

10.1002/chin.199713165 ◽

2010 ◽

Vol 28 (13) ◽

pp. no-no ◽

Cited By ~ 1

Author(s):

T. HONDA ◽

M. KATOH ◽

S. YAMANE

Keyword(s):

Stereoselective Synthesis ◽

Formal Synthesis

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ChemInform Abstract: Stereoselective Synthesis of 2-Amino-2,5-dideoxy-L-lyxo-pentanoate. Formal Synthesis of L-Daunosamine.

ChemInform ◽

10.1002/chin.198744328 ◽

1987 ◽

Vol 18 (44) ◽

Author(s):

S. CARDANI

Keyword(s):

Stereoselective Synthesis ◽

Formal Synthesis

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Stereoselective Synthesis of Unsymmetrical β,β-Diarylacrylates by a Heck−Matsuda Reaction: Versatile Building Blocks for Asymmetric Synthesis of β,β-Diphenylpropanoates, 3-Aryl-indole, and 4-Aryl-3,4-dihydro-quinolin-2-one and Formal Synthesis of (−)-Indatraline

The Journal of Organic Chemistry ◽

10.1021/jo102134v ◽

2011 ◽

Vol 76 (3) ◽

pp. 857-869 ◽

Cited By ~ 55

Author(s):

Jason G. Taylor ◽

Carlos Roque D. Correia

Keyword(s):

Asymmetric Synthesis ◽

Stereoselective Synthesis ◽

Building Blocks ◽

Formal Synthesis

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ChemInform Abstract: Nickel and Palladium Catalysis in the Stereoselective Synthesis of Functionalized Pyrrolidines: Enantioselective Formal Synthesis of (+)-α-Allokainic Acid.

ChemInform ◽

10.1002/chin.199917210 ◽

2010 ◽

Vol 30 (17) ◽

pp. no-no

Author(s):

Maxim V. Chevliakov ◽

John Montgomery

Keyword(s):

Stereoselective Synthesis ◽

Palladium Catalysis ◽

Formal Synthesis

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ChemInform Abstract: Selenium-Controlled Stereoselective Synthesis of 2′-Deoxynucleosides from Glycals. A Formal Synthesis of AZT.

ChemInform ◽

10.1002/chin.199339293 ◽

2010 ◽

Vol 24 (39) ◽

pp. no-no

Author(s):

A. EL-LAGHDACH ◽

Y. DIAZ ◽

S. CASTILLON

Keyword(s):

Stereoselective Synthesis ◽

Formal Synthesis

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ChemInform Abstract: New Methods and Reagents in Organic Synthesis. Part 90. A New Stereoselective Synthesis of a γ-Azetidinyl-β-hydroxy-. alpha.-amino Acid Moiety of Mugineic Acid (I). A Formal Synthesis of Mugineic Acid.

ChemInform ◽

10.1002/chin.199149147 ◽

2010 ◽

Vol 22 (49) ◽

pp. no-no

Author(s):

Y. HAMADA ◽

K. IWAI ◽

T. SHIOIRI

Keyword(s):

Amino Acid ◽

Organic Synthesis ◽

Stereoselective Synthesis ◽

Acid Moiety ◽

Formal Synthesis ◽

Mugineic Acid ◽

New Methods ◽

Amino Acid Moiety ◽

Alpha Amino Acid

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Stereoselective synthesis of petrosterol and a formal synthesis of aragusterols

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19960002291 ◽

1996 ◽

pp. 2291 ◽

Cited By ~ 12

Author(s):

Toshio Honda ◽

Miho Katoh ◽

Shin-ichi Yamane

Keyword(s):

Stereoselective Synthesis ◽

Formal Synthesis

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N-tert-Butanesulfinyl Imines in Alkaloid Synthesis: Stereoselective Synthesis of (R)-Coniine and Formal Synthesis of (S)-δ-Coniceine¹

Synthesis ◽

10.1055/s-0030-1260117 ◽

2011 ◽

Vol 2011 (15) ◽

pp. 2478-2482 ◽

Cited By ~ 2

Author(s):

Biswanath Das ◽

Kongara Damodar ◽

Maram Lingaiah ◽

Nisith Bhunia

Keyword(s):

Stereoselective Synthesis ◽

Formal Synthesis ◽

Alkaloid Synthesis

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Stereoselective synthesis of trans-THF rings using an oxidative cyclisation-radical deoxygenation sequence: application to the formal synthesis of trans-(2R,5R)-linalool oxide

RSC Advances ◽

10.1039/c4ra13258k ◽

2015 ◽

Vol 5 (6) ◽

pp. 3941-3953 ◽

Cited By ~ 3

Author(s):

Nadeem S. Sheikh

Keyword(s):

Stereoselective Synthesis ◽

Formal Synthesis ◽

Linalool Oxide ◽

Oxidative Cyclisation

Permanganate-mediated oxidative cyclisation-Barton–McCombie radical deoxygenation sequence is applied to 1,5-dienes to achieve stereoselective synthesis of trans-2,5-disubstituted THF rings.

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Stereoselective Synthesis of C-6 Substituted Pipecolic Acid Derivatives. Formal Synthesis of (+)-Indolizidine 167B and (+)-Indolizidine 209D.

ChemInform ◽

10.1002/chin.200305204 ◽

2003 ◽

Vol 34 (5) ◽

Author(s):

Sylvie Carbonnel ◽

Yves Troin

Keyword(s):

Stereoselective Synthesis ◽

Pipecolic Acid ◽

Formal Synthesis

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Stereoselective synthesis of (3R*,3aS*,7aS*)-3-aryloctahydroindol-2-ones using radical cyclisation: a formal synthesis of (±)-pancracine

ChemInform Abstract: Stereoselective Synthesis of Petrosterol and a Formal Synthesis of Aragusterols.

ChemInform Abstract: Stereoselective Synthesis of 2-Amino-2,5-dideoxy-L-lyxo-pentanoate. Formal Synthesis of L-Daunosamine.

Stereoselective Synthesis of Unsymmetrical β,β-Diarylacrylates by a Heck−Matsuda Reaction: Versatile Building Blocks for Asymmetric Synthesis of β,β-Diphenylpropanoates, 3-Aryl-indole, and 4-Aryl-3,4-dihydro-quinolin-2-one and Formal Synthesis of (−)-Indatraline

ChemInform Abstract: Nickel and Palladium Catalysis in the Stereoselective Synthesis of Functionalized Pyrrolidines: Enantioselective Formal Synthesis of (+)-α-Allokainic Acid.

ChemInform Abstract: Selenium-Controlled Stereoselective Synthesis of 2′-Deoxynucleosides from Glycals. A Formal Synthesis of AZT.

ChemInform Abstract: New Methods and Reagents in Organic Synthesis. Part 90. A New Stereoselective Synthesis of a γ-Azetidinyl-β-hydroxy-. alpha.-amino Acid Moiety of Mugineic Acid (I). A Formal Synthesis of Mugineic Acid.

Stereoselective synthesis of petrosterol and a formal synthesis of aragusterols

N-tert-Butanesulfinyl Imines in Alkaloid Synthesis: Stereoselective Synthesis of (R)-Coniine and Formal Synthesis of (S)-δ-Coniceine¹

Stereoselective synthesis of trans-THF rings using an oxidative cyclisation-radical deoxygenation sequence: application to the formal synthesis of trans-(2R,5R)-linalool oxide

Stereoselective Synthesis of C-6 Substituted Pipecolic Acid Derivatives. Formal Synthesis of (+)-Indolizidine 167B and (+)-Indolizidine 209D.

Stereoselective synthesis of (3R,3aS,7aS*)-3-aryloctahydroindol-2-ones using radical cyclisation: a formal synthesis of (±)-pancracine