Stereoselective synthesis of the C7-C21 segment of epothilone A via asymmetric alkoxyallyl- and crotylboration

P. Veeraraghavan Ramachandran; Bodhuri Prabhudas; Debarshi Pratihar; J. Subash Chandra; M. Venkat Ram Reddy

doi:10.1016/S0040-4039(03)00748-2

Stereoselective synthesis of the C₇-C₂₁ segment of epothilone A via asymmetric alkoxyallyl- and crotylboration

P. Veeraraghavan Ramachandran
, Bodhuri Prabhudas
, Debarshi Pratihar
, J. Subash Chandra
, M. Venkat Ram Reddy

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

22 Scopus citations

Abstract

The synthesis of the C₇-C₂₁ fragment of epothilone A involving asymmetric alkoxyallyl- and crotylboration using α-pinene-derived reagents is described.

Original language	English (US)
Pages (from-to)	3745-3748
Number of pages	4
Journal	Tetrahedron Letters
Volume	44
Issue number	19
DOIs	https://doi.org/10.1016/S0040-4039(03)00748-2
State	Published - May 5 2003
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(03)00748-2

Cite this

@article{be48c71cb1b84988918c9a690cab4188,

title = "Stereoselective synthesis of the C7-C21 segment of epothilone A via asymmetric alkoxyallyl- and crotylboration",

abstract = "The synthesis of the C7-C21 fragment of epothilone A involving asymmetric alkoxyallyl- and crotylboration using α-pinene-derived reagents is described.",

author = "Ramachandran, \{P. Veeraraghavan\} and Bodhuri Prabhudas and Debarshi Pratihar and Chandra, \{J. Subash\} and Reddy, \{M. Venkat Ram\}",

note = "Funding Information: Financial support from the Herbert C. Brown Center for Borane Research and Aldrich Chemical Company is greatly acknowledged. ",

year = "2003",

month = may,

day = "5",

doi = "10.1016/S0040-4039(03)00748-2",

language = "English (US)",

volume = "44",

pages = "3745--3748",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "19",

}

TY - JOUR

T1 - Stereoselective synthesis of the C7-C21 segment of epothilone A via asymmetric alkoxyallyl- and crotylboration

AU - Ramachandran, P. Veeraraghavan

AU - Prabhudas, Bodhuri

AU - Pratihar, Debarshi

AU - Chandra, J. Subash

AU - Reddy, M. Venkat Ram

N1 - Funding Information: Financial support from the Herbert C. Brown Center for Borane Research and Aldrich Chemical Company is greatly acknowledged.

PY - 2003/5/5

Y1 - 2003/5/5

N2 - The synthesis of the C7-C21 fragment of epothilone A involving asymmetric alkoxyallyl- and crotylboration using α-pinene-derived reagents is described.

AB - The synthesis of the C7-C21 fragment of epothilone A involving asymmetric alkoxyallyl- and crotylboration using α-pinene-derived reagents is described.

UR - https://www.scopus.com/pages/publications/0037420764

UR - https://www.scopus.com/pages/publications/0037420764#tab=citedBy

U2 - 10.1016/S0040-4039(03)00748-2

DO - 10.1016/S0040-4039(03)00748-2

M3 - Article

AN - SCOPUS:0037420764

SN - 0040-4039

VL - 44

SP - 3745

EP - 3748

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 19

ER -

Stereoselective synthesis of the C₇-C₂₁ segment of epothilone A via asymmetric alkoxyallyl- and crotylboration

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this