Hydroboration/amination of n-trimethylsilyl protected olefinic amines and diolefins: Synthesis of isomerically pure diamines

George Kabalka, Zhe Wang

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

N-Trimethylsilyl protected olefinic amines and terminal diolefins were hydroborated with dimethylborane and the resulting organoboranes were treated with in situ generated chloramine or chloroalkylamines to produce isomerically pure diamines or N-substituted diamines in good yields.

Original languageEnglish (US)
Pages (from-to)2113-2118
Number of pages6
JournalSynthetic Communications
Volume20
Issue number14
DOIs
StatePublished - Jul 1 1990

Fingerprint

Alkadienes
Amination
Diamines
Amines

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Hydroboration/amination of n-trimethylsilyl protected olefinic amines and diolefins : Synthesis of isomerically pure diamines. / Kabalka, George; Wang, Zhe.

In: Synthetic Communications, Vol. 20, No. 14, 01.07.1990, p. 2113-2118.

Research output: Contribution to journalArticle

@article{b21952c0958144fba1eb65cacbb3336b,
title = "Hydroboration/amination of n-trimethylsilyl protected olefinic amines and diolefins: Synthesis of isomerically pure diamines",
abstract = "N-Trimethylsilyl protected olefinic amines and terminal diolefins were hydroborated with dimethylborane and the resulting organoboranes were treated with in situ generated chloramine or chloroalkylamines to produce isomerically pure diamines or N-substituted diamines in good yields.",
author = "George Kabalka and Zhe Wang",
year = "1990",
month = "7",
day = "1",
doi = "10.1080/00397919008053146",
language = "English (US)",
volume = "20",
pages = "2113--2118",
journal = "Synthetic Communications",
issn = "0039-7911",
publisher = "Taylor and Francis Ltd.",
number = "14",

}

TY - JOUR

T1 - Hydroboration/amination of n-trimethylsilyl protected olefinic amines and diolefins

T2 - Synthesis of isomerically pure diamines

AU - Kabalka, George

AU - Wang, Zhe

PY - 1990/7/1

Y1 - 1990/7/1

N2 - N-Trimethylsilyl protected olefinic amines and terminal diolefins were hydroborated with dimethylborane and the resulting organoboranes were treated with in situ generated chloramine or chloroalkylamines to produce isomerically pure diamines or N-substituted diamines in good yields.

AB - N-Trimethylsilyl protected olefinic amines and terminal diolefins were hydroborated with dimethylborane and the resulting organoboranes were treated with in situ generated chloramine or chloroalkylamines to produce isomerically pure diamines or N-substituted diamines in good yields.

UR - http://www.scopus.com/inward/record.url?scp=84972952102&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84972952102&partnerID=8YFLogxK

U2 - 10.1080/00397919008053146

DO - 10.1080/00397919008053146

M3 - Article

AN - SCOPUS:84972952102

VL - 20

SP - 2113

EP - 2118

JO - Synthetic Communications

JF - Synthetic Communications

SN - 0039-7911

IS - 14

ER -