Organolanthanide-Catalyzed Cyclization/Boration of 1,5- and 1,6-Dienes

Gary A. Molander; Dirk Pfeiffer

doi:10.1021/ol006841s

Organolanthanide-Catalyzed Cyclization/Boration of 1,5- and 1,6-Dienes

Gary A. Molander, Dirk Pfeiffer

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

59 Citations (Scopus)

Abstract

(Matrix Presented) 1,5- and 1,6-Dienes undergo a cyclization/boration reaction in the presence of a catalytic amount of Cp*₂Sm·THF. The resulting organoboranes can be oxidized to the corresponding primary cyclic alcohols using standard conditions.

Original language	English
Pages (from-to)	361-363
Journal	Organic Letters
Volume	3
Issue number	3
DOIs	https://doi.org/10.1021/ol006841s
Publication status	Published - 8 Feb 2001
Externally published	Yes

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@article{1c870a48a03c44c8a5cd45e7b152c1fb,

title = "Organolanthanide-Catalyzed Cyclization/Boration of 1,5- and 1,6-Dienes",

abstract = "(Matrix Presented) 1,5- and 1,6-Dienes undergo a cyclization/boration reaction in the presence of a catalytic amount of Cp*2Sm·THF. The resulting organoboranes can be oxidized to the corresponding primary cyclic alcohols using standard conditions.",

author = "Molander, {Gary A.} and Dirk Pfeiffer",

year = "2001",

month = feb,

day = "8",

doi = "10.1021/ol006841s",

language = "English",

volume = "3",

pages = "361--363",

journal = "Organic Letters",

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publisher = "American Chemical Society",

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T1 - Organolanthanide-Catalyzed Cyclization/Boration of 1,5- and 1,6-Dienes

AU - Molander, Gary A.

AU - Pfeiffer, Dirk

PY - 2001/2/8

Y1 - 2001/2/8

N2 - (Matrix Presented) 1,5- and 1,6-Dienes undergo a cyclization/boration reaction in the presence of a catalytic amount of Cp*2Sm·THF. The resulting organoboranes can be oxidized to the corresponding primary cyclic alcohols using standard conditions.

AB - (Matrix Presented) 1,5- and 1,6-Dienes undergo a cyclization/boration reaction in the presence of a catalytic amount of Cp*2Sm·THF. The resulting organoboranes can be oxidized to the corresponding primary cyclic alcohols using standard conditions.

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UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-0035825773&origin=recordpage

U2 - 10.1021/ol006841s

DO - 10.1021/ol006841s

M3 - RGC 21 - Publication in refereed journal

C2 - 11428014

SN - 1523-7060

VL - 3

SP - 361

EP - 363

JO - Organic Letters

JF - Organic Letters

IS - 3

ER -

Organolanthanide-Catalyzed Cyclization/Boration of 1,5- and 1,6-Dienes

Abstract

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