Intramolecular 1,3-diyl trapping reactions. Use of a diylophile directly linked to the diyl. Preparation of bicyclic furans.

Kevin D. Moeller; R. Daniel Little

doi:10.1016/S0040-4039(00)98652-0

Intramolecular 1,3-diyl trapping reactions. Use of a diylophile directly linked to the diyl. Preparation of bicyclic furans.

Kevin D. Moeller
, R. Daniel Little

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

15 Scopus citations

Abstract

The chemistry of diazenes 1-3, each of which possesses a diylophile directly linked by a CC bond to a latent 1,3-diyl, was investigated. Each undergoes a loss of nitrogen and conversion to products 4-6 respectively.

Original language	English
Pages (from-to)	3417-3420
Number of pages	4
Journal	Tetrahedron Letters
Volume	26
Issue number	29
DOIs	https://doi.org/10.1016/S0040-4039(00)98652-0
State	Published - 1985

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title = "Intramolecular 1,3-diyl trapping reactions. Use of a diylophile directly linked to the diyl. Preparation of bicyclic furans.",

abstract = "The chemistry of diazenes 1-3, each of which possesses a diylophile directly linked by a CC bond to a latent 1,3-diyl, was investigated. Each undergoes a loss of nitrogen and conversion to products 4-6 respectively.",

author = "Moeller, \{Kevin D.\} and \{Daniel Little\}, R.",

year = "1985",

doi = "10.1016/S0040-4039(00)98652-0",

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T1 - Intramolecular 1,3-diyl trapping reactions. Use of a diylophile directly linked to the diyl. Preparation of bicyclic furans.

AU - Moeller, Kevin D.

AU - Daniel Little, R.

PY - 1985

Y1 - 1985

N2 - The chemistry of diazenes 1-3, each of which possesses a diylophile directly linked by a CC bond to a latent 1,3-diyl, was investigated. Each undergoes a loss of nitrogen and conversion to products 4-6 respectively.

AB - The chemistry of diazenes 1-3, each of which possesses a diylophile directly linked by a CC bond to a latent 1,3-diyl, was investigated. Each undergoes a loss of nitrogen and conversion to products 4-6 respectively.

UR - https://www.scopus.com/pages/publications/0010620515

U2 - 10.1016/S0040-4039(00)98652-0

DO - 10.1016/S0040-4039(00)98652-0

M3 - Article

AN - SCOPUS:0010620515

SN - 0040-4039

VL - 26

SP - 3417

EP - 3420

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 29

ER -

Intramolecular 1,3-diyl trapping reactions. Use of a diylophile directly linked to the diyl. Preparation of bicyclic furans.

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