Approach to the synthesis of nogalarol via the cycloaddition of a carbene-chromium complex with a functionalized alkyne

M. F. Semmelhack; Nakcheol Jeong

doi:10.1016/S0040-4039(00)94579-9

Approach to the synthesis of nogalarol via the cycloaddition of a carbene-chromium complex with a functionalized alkyne

M. F. Semmelhack, Nakcheol Jeong

Chemistry

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

25 Scopus citations

Abstract

The alkyne, 4, prepared stereoselectively in 7 steps from acetyl furan, reacts with (methoxy)(phenyl)carbenepentacarbonylchromium(0), 15, to give the model (16) for nogalarol (1b) in 43% yield.

Original language	English (US)
Pages (from-to)	605-608
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	5
DOIs	https://doi.org/10.1016/S0040-4039(00)94579-9
State	Published - 1990

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)94579-9

Cite this

@article{32187b8118d541648279232c58efd06d,

title = "Approach to the synthesis of nogalarol via the cycloaddition of a carbene-chromium complex with a functionalized alkyne",

abstract = "The alkyne, 4, prepared stereoselectively in 7 steps from acetyl furan, reacts with (methoxy)(phenyl)carbenepentacarbonylchromium(0), 15, to give the model (16) for nogalarol (1b) in 43% yield.",

author = "Semmelhack, {M. F.} and Nakcheol Jeong",

year = "1990",

doi = "10.1016/S0040-4039(00)94579-9",

language = "English (US)",

volume = "31",

pages = "605--608",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "5",

}

TY - JOUR

T1 - Approach to the synthesis of nogalarol via the cycloaddition of a carbene-chromium complex with a functionalized alkyne

AU - Semmelhack, M. F.

AU - Jeong, Nakcheol

PY - 1990

Y1 - 1990

N2 - The alkyne, 4, prepared stereoselectively in 7 steps from acetyl furan, reacts with (methoxy)(phenyl)carbenepentacarbonylchromium(0), 15, to give the model (16) for nogalarol (1b) in 43% yield.

AB - The alkyne, 4, prepared stereoselectively in 7 steps from acetyl furan, reacts with (methoxy)(phenyl)carbenepentacarbonylchromium(0), 15, to give the model (16) for nogalarol (1b) in 43% yield.

UR - http://www.scopus.com/inward/record.url?scp=0025057506&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025057506&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)94579-9

DO - 10.1016/S0040-4039(00)94579-9

M3 - Article

AN - SCOPUS:0025057506

SN - 0040-4039

VL - 31

SP - 605

EP - 608

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 5

ER -

Approach to the synthesis of nogalarol via the cycloaddition of a carbene-chromium complex with a functionalized alkyne

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this