Total synthesis of preswinholide A. 2. Completion of the synthesis

Kazuo Nagasawa; Isao Shimizu; Tadashi Nakata

doi:10.1016/0040-4039(96)01504-3

Total synthesis of preswinholide A. 2. Completion of the synthesis

Kazuo Nagasawa, Isao Shimizu, Tadashi Nakata^*

^*Corresponding author for this work

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

16 Citations (Scopus)

Abstract

Total synthesis of preswinholide A was stereoseletively accomplished through the aldol coupling reaction of the C11-C23 and C24-C32 segments and stereoselective introduction of the 9α side chain and 7β-hydroxyl group.

Original language	English
Pages (from-to)	6885-6888
Number of pages	4
Journal	Tetrahedron Letters
Volume	37
Issue number	38
DOIs	https://doi.org/10.1016/0040-4039(96)01504-3
Publication status	Published - 1996 Sept 16

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

Access to Document

10.1016/0040-4039(96)01504-3

Cite this

@article{58867403b9024fd88539631c6682cdda,

title = "Total synthesis of preswinholide A. 2. Completion of the synthesis",

abstract = "Total synthesis of preswinholide A was stereoseletively accomplished through the aldol coupling reaction of the C11-C23 and C24-C32 segments and stereoselective introduction of the 9α side chain and 7β-hydroxyl group.",

author = "Kazuo Nagasawa and Isao Shimizu and Tadashi Nakata",

year = "1996",

month = sep,

day = "16",

doi = "10.1016/0040-4039(96)01504-3",

language = "English",

volume = "37",

pages = "6885--6888",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "38",

}

TY - JOUR

T1 - Total synthesis of preswinholide A. 2. Completion of the synthesis

AU - Nagasawa, Kazuo

AU - Shimizu, Isao

AU - Nakata, Tadashi

PY - 1996/9/16

Y1 - 1996/9/16

N2 - Total synthesis of preswinholide A was stereoseletively accomplished through the aldol coupling reaction of the C11-C23 and C24-C32 segments and stereoselective introduction of the 9α side chain and 7β-hydroxyl group.

AB - Total synthesis of preswinholide A was stereoseletively accomplished through the aldol coupling reaction of the C11-C23 and C24-C32 segments and stereoselective introduction of the 9α side chain and 7β-hydroxyl group.

UR - http://www.scopus.com/inward/record.url?scp=16044366589&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=16044366589&partnerID=8YFLogxK

U2 - 10.1016/0040-4039(96)01504-3

DO - 10.1016/0040-4039(96)01504-3

M3 - Article

AN - SCOPUS:16044366589

SN - 0040-4039

VL - 37

SP - 6885

EP - 6888

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 38

ER -

Total synthesis of preswinholide A. 2. Completion of the synthesis

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this