Synthetic Study towards Taurospongin A: Wittig Olefination Approach to the Core Structure

Guang Rong Zheng; Wei Lu; Jun Chao Cai

Synthetic Study towards Taurospongin A: Wittig Olefination Approach to the Core Structure

Guang Rong Zheng, Wei Lu, Jun Chao Cai

CAS - Shanghai Institute of Materia Medica

Research output: Contribution to journal › Article › peer-review

4 Scopus citations

Abstract

An efficient, convergent and enantioselective synthetic approach to the trihydroxy core structure 2 of Taurospongin A 1 is described. The featured step is a classic Wittig coupling reaction between C1-C4 aldehyde segment 4 and C5-C10 phosphate salt segment (5).

Original language	English
Pages (from-to)	961-964
Number of pages	4
Journal	Chinese Chemical Letters
Volume	12
Issue number	11
State	Published - Nov 2001
Externally published	Yes

Keywords

Enantioselective synthesis
Taurospongin A
Wittig olefination

Cite this

@article{511db249b2d34ee0887314ce43d02d50,

title = "Synthetic Study towards Taurospongin A: Wittig Olefination Approach to the Core Structure",

abstract = "An efficient, convergent and enantioselective synthetic approach to the trihydroxy core structure 2 of Taurospongin A 1 is described. The featured step is a classic Wittig coupling reaction between C1-C4 aldehyde segment 4 and C5-C10 phosphate salt segment (5).",

keywords = "Enantioselective synthesis, Taurospongin A, Wittig olefination",

author = "Zheng, \{Guang Rong\} and Wei Lu and Cai, \{Jun Chao\}",

year = "2001",

month = nov,

language = "英语",

volume = "12",

pages = "961--964",

journal = "Chinese Chemical Letters",

issn = "1001-8417",

publisher = "Elsevier B.V.",

number = "11",

}

TY - JOUR

T1 - Synthetic Study towards Taurospongin A

T2 - Wittig Olefination Approach to the Core Structure

AU - Zheng, Guang Rong

AU - Lu, Wei

AU - Cai, Jun Chao

PY - 2001/11

Y1 - 2001/11

N2 - An efficient, convergent and enantioselective synthetic approach to the trihydroxy core structure 2 of Taurospongin A 1 is described. The featured step is a classic Wittig coupling reaction between C1-C4 aldehyde segment 4 and C5-C10 phosphate salt segment (5).

AB - An efficient, convergent and enantioselective synthetic approach to the trihydroxy core structure 2 of Taurospongin A 1 is described. The featured step is a classic Wittig coupling reaction between C1-C4 aldehyde segment 4 and C5-C10 phosphate salt segment (5).

KW - Enantioselective synthesis

KW - Taurospongin A

KW - Wittig olefination

UR - https://www.scopus.com/pages/publications/0035623876

M3 - 文章

AN - SCOPUS:0035623876

SN - 1001-8417

VL - 12

SP - 961

EP - 964

JO - Chinese Chemical Letters

JF - Chinese Chemical Letters

IS - 11

ER -

Synthetic Study towards Taurospongin A: Wittig Olefination Approach to the Core Structure

Abstract

Keywords

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