A General, Convergent Strategy for the Construction of Indolizidine Alkaloids:  Total Syntheses of (−)-Indolizidine 223AB and Alkaloid (−)-205B†

Amos B. Smith; Dae-Shik Kim

doi:10.1021/jo052314g

A General, Convergent Strategy for the Construction of Indolizidine Alkaloids: Total Syntheses of (−)-Indolizidine 223AB and Alkaloid (−)-205B†

The Journal of Organic Chemistry ◽

10.1021/jo052314g ◽

2006 ◽

Vol 71 (7) ◽

pp. 2547-2557 ◽

Cited By ~ 95

Author(s):

Amos B. Smith ◽

Dae-Shik Kim

Keyword(s):

Indolizidine Alkaloids ◽

Total Syntheses ◽

Indolizidine 223Ab

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A General, Convergent Strategy for the Construction of Indolizidine Alkaloids: Total Syntheses of (-)-Indolizidine 223AB (I) and Alkaloid (-)-205B (II).

ChemInform ◽

10.1002/chin.200635213 ◽

2006 ◽

Vol 37 (35) ◽

Author(s):

Amos B. III Smith ◽

Dae-Shik Kim

Keyword(s):

Indolizidine Alkaloids ◽

Total Syntheses ◽

Indolizidine 223Ab

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One-Pot Preparation of Quinolizidin-2-one and Indolizidin-7-one Ring Systems. Concise Total Syntheses of (.+-.)-Myrtine, (.+-.)-Lasubine II, and (-)-Indolizidine 223AB

The Journal of Organic Chemistry ◽

10.1021/jo00108a040 ◽

1995 ◽

Vol 60 (3) ◽

pp. 717-722 ◽

Cited By ~ 65

Author(s):

Ronaldo A. Pilli ◽

Luiz Carlos Dias ◽

Adriano O. Maldaner

Keyword(s):

One Pot ◽

Ring Systems ◽

Total Syntheses ◽

Indolizidine 223Ab

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Enantioselective total syntheses of indolizidine alkaloids 167B and 209D

The Journal of Organic Chemistry ◽

10.1021/jo00302a038 ◽

1990 ◽

Vol 55 (15) ◽

pp. 4688-4693 ◽

Cited By ~ 92

Author(s):

Richard P. Polniaszek ◽

Stephen E. Belmont

Keyword(s):

Indolizidine Alkaloids ◽

Total Syntheses

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ChemInform Abstract: One-Pot Preparation of Quinolizidin-2-one and Indolizidin-7-one Ring Systems. Concise Total Syntheses of (.+-.)-Myrtine, (.+-.)-Lasubine II, and (-)-Indolizidine 223AB.

ChemInform ◽

10.1002/chin.199530252 ◽

2010 ◽

Vol 26 (30) ◽

pp. no-no

Author(s):

R. A. PILLI ◽

L. C. DIAS ◽

A. O. MALDANER

Keyword(s):

One Pot ◽

Ring Systems ◽

Total Syntheses ◽

Indolizidine 223Ab

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Enantioselective total syntheses of indolizidine alkaloids (-)-205A and (-)-235B

The Journal of Organic Chemistry ◽

10.1021/jo00016a013 ◽

1991 ◽

Vol 56 (16) ◽

pp. 4868-4874 ◽

Cited By ~ 44

Author(s):

Richard P. Polniaszek ◽

Stephen E. Belmont

Keyword(s):

Indolizidine Alkaloids ◽

Total Syntheses

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Enantiopure 2,6-disubstituted piperidines bearing one alkene- or alkyne-containing substituent: preparation and application to total syntheses of indolizidine-alkaloids

Organic & Biomolecular Chemistry ◽

10.1039/b927007h ◽

2010 ◽

Vol 8 (8) ◽

pp. 1899 ◽

Cited By ~ 30

Author(s):

Hui Liu ◽

Deyong Su ◽

Guolin Cheng ◽

Jimin Xu ◽

Xinyan Wang ◽

...

Keyword(s):

Indolizidine Alkaloids ◽

Total Syntheses

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Bicyclo[3.3.1]nonanes as synthetic intermediates. Part 20.1 Asymmetric synthesis of the indolizidine alkaloids monomorine I and indolizidine 223AB

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/a607981d ◽

1997 ◽

pp. 1315-1322 ◽

Cited By ~ 20

Author(s):

Takefumi Momose ◽

Minoru Toshima ◽

Sumie Seki ◽

Yayoi Koike ◽

Naoki Toyooka ◽

...

Keyword(s):

Asymmetric Synthesis ◽

Indolizidine Alkaloids ◽

Synthetic Intermediates ◽

Indolizidine 223Ab

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ChemInform Abstract: Enantiopure 2,6-Disubstituted Piperidines Bearing One Alkene- or Alkyne-Containing Substituent: Preparation and Application to Total Syntheses of Indolizidine-Alkaloids.

ChemInform ◽

10.1002/chin.201036197 ◽

2010 ◽

Vol 41 (36) ◽

pp. no-no

Author(s):

Hui Liu ◽

Deyong Su ◽

Guolin Cheng ◽

Jimin Xu ◽

Xinyan Wang ◽

...

Keyword(s):

Indolizidine Alkaloids ◽

Total Syntheses

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ChemInform Abstract: Bicyclo(3.3.1)nonanes as Synthetic Intermediates. Part 20. Asymmetric Synthesis of the Indolizidine Alkaloids Monomorine I and Indolizidine 223AB.

ChemInform ◽

10.1002/chin.199741264 ◽

2010 ◽

Vol 28 (41) ◽

pp. no-no

Author(s):

T. MOMOSE ◽

M. TOSHIMA ◽

S. SEKI ◽

Y. KOIKE ◽

N. TOYOOKA ◽

...

Keyword(s):

Asymmetric Synthesis ◽

Indolizidine Alkaloids ◽

Synthetic Intermediates ◽

Indolizidine 223Ab

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Development of Recent Total Syntheses Based on the Heck Reaction

Current Organic Chemistry ◽

10.2174/13852728113179990032 ◽

2013 ◽

Vol 17 (19) ◽

pp. 2192-2224 ◽

Cited By ~ 48

Author(s):

Majid Heravi ◽

Elaheh Hashemi ◽

Nazanin Ghobadi

Keyword(s):

Heck Reaction ◽

Total Syntheses

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