A total synthesis of (−)-reiswigin a via sequential claisen rearrangement-intramolecular ester enolate alkylation

Tetrahedron Letters ◽

10.1016/0040-4039(94)80021-9 ◽

1994 ◽

Vol 35 (43) ◽

pp. 7957-7960 ◽

Author(s):

Deukjoon Kim ◽

Kye Jung Shin ◽

Ik Yoen Kim ◽

Sang Woo Park

Keyword(s):

Total Synthesis ◽

Claisen Rearrangement ◽

Enolate Alkylation ◽

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A total synthesis of (−)-reiswigin a via sequential claisen rearrangement-intramolecular ester enolate alkylation

Tetrahedron Letters ◽

10.1016/s0040-4039(00)78395-x ◽

1994 ◽

Vol 35 (41) ◽

pp. 7957-7960 ◽

Author(s):

D Kim

Keyword(s):

Total Synthesis ◽

Claisen Rearrangement ◽

Enolate Alkylation ◽

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ChemInform Abstract: A Total Synthesis of (-)-Reiswigin A via Sequential Claisen Rearrangement-Intramolecular Ester Enolate Alkylation.

10.1002/chin.199513241 ◽

2010 ◽

Vol 26 (13) ◽

pp. no-no

Author(s):

D. KIM ◽

K. J. SHIN ◽

I. Y. KIM ◽

S. W. PARK

Keyword(s):

Total Synthesis ◽

Claisen Rearrangement ◽

Enolate Alkylation ◽

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A stereoselective asymmetric synthesis of antibiotic (-)-Fumagillol using claisen rearrangement and intramolecular ester enolate alkylation as key steps

Archives of Pharmacal Research ◽

10.1007/bf02977704 ◽

2005 ◽

Vol 28 (2) ◽

pp. 129-141 ◽

Author(s):

Deukjoon Kim ◽

Soon Kil Ahn ◽

Hoon Bae ◽

Hak Sung Kim

Keyword(s):

Asymmetric Synthesis ◽

Claisen Rearrangement ◽

Enolate Alkylation ◽

Ester Enolate ◽

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A stereoselective total synthesis of (±)-oppositol by a doubly diastereoselective intramolecular ester enolate alkylation

Tetrahedron Letters ◽

10.1016/s0040-4039(96)02313-1 ◽

1997 ◽

Vol 38 (3) ◽

pp. 415-416 ◽

Author(s):

Deukjoon Kim ◽

In Ho Kim

Keyword(s):

Total Synthesis ◽

Enolate Alkylation ◽

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ChemInform Abstract: A Stereoselective Total Synthesis of (.+-.)-Oppositol by a Doubly Diastereoselective Intramolecular Ester Enolate Alkylation.

10.1002/chin.199720151 ◽

2010 ◽

Vol 28 (20) ◽

pp. no-no

Author(s):

D. KIM ◽

I. H. KIM

Keyword(s):

Total Synthesis ◽

Enolate Alkylation ◽

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The ester enolate claisen rearrangement. Total synthesis of (±)-ethisolide

Tetrahedron Letters ◽

10.1016/s0040-4039(00)85501-x ◽

1986 ◽

Vol 27 (4) ◽

pp. 445-448 ◽

Author(s):

Steven D. Burke ◽

Gregory J. Pacofsky

Keyword(s):

Total Synthesis ◽

Claisen Rearrangement ◽

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Proline Ester Enolate Claisen Rearrangement and Formal Total Synthesis of (−)-Cephalotaxine

The Journal of Organic Chemistry ◽

10.1021/acs.joc.9b00933 ◽

2019 ◽

Vol 84 (12) ◽

pp. 8080-8089 ◽

Author(s):

Hongjun Jeon ◽

Yundong Chung ◽

Sanghee Kim

Keyword(s):

Total Synthesis ◽

Claisen Rearrangement ◽

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ChemInform Abstract: The Ester Enolate Claisen Rearrangement. Total Synthesis of (±)-Ethisolide.

Chemischer Informationsdienst ◽

10.1002/chin.198623351 ◽

1986 ◽

Vol 17 (23) ◽

Author(s):

S. D. BURKE ◽

G. J. PACOFSKY ◽

C. W. MURTIASHAW

Keyword(s):

Total Synthesis ◽

Claisen Rearrangement ◽

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Total Synthesis of Icaritin via Microwave-assistance Claisen Rearrangement

Letters in Organic Chemistry ◽

10.2174/157017861109140903103927 ◽

2014 ◽

Vol 11 (9) ◽

pp. 677-681 ◽

Author(s):

Van-Son Nguyen ◽

Ling Shi ◽

Yue Li ◽

Qiu-An Wang

Keyword(s):

Total Synthesis ◽

Claisen Rearrangement ◽

Microwave Assistance

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1,8-Stereocontrol by 1,5-induction using an allylstannane followed by Ireland-Claisen rearrangement: Diastereoselective total synthesis of (±)-patulolide C

Tetrahedron Letters ◽

10.1016/s0040-4039(98)02427-7 ◽

1999 ◽

Vol 40 (3) ◽

pp. 471-474 ◽

Author(s):

E. Kate Dorling ◽

Eric J. Thomas

Keyword(s):

Total Synthesis ◽

Claisen Rearrangement

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