The β-heteroatom effect on carbenes

DOI: 10.1016/S0040-4020(97)00341-4

Source and publish data:

Tetrahedron p. 9989 - 9996 (1997)

Update date:2022-07-31

Topics:

Authors:

Lambert, Joseph B.

Liu, Xiaoyang

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4020(97)00341-4

The β-thiophosphinoyl carbene PhCCH₂P(S)Ph₂ (5) has been prepared by irradiation of the corresponding diazo compound. The relative rates for insertion into the OH bond of methanol and for addition to the double bond of 2-methyl-2-but

Full text of DOI:10.1016/S0040-4020(97)00341-4

Products guided by the article

Product name:diphenyl(benzoylmethyl)phosphine sulfide p-toluenesulfonylhydrazone

Cas No:194668-41-2

R&D Labs maybe for 194668-41-2

Shaanxi King Stone Enterprise Company Limited

Contact:86-29-88353805,13609285751

Address:.209 Keji Road Hi-Tech industrial Develpment Zone .Xian China
Shanghai Demand Chemical Co., ltd，China

Contact:86-021-55237578/55239122

Address:Room 3H, No.578, Yingkou Road, Yangpu District, Shanghai, China
Zibo Jujin Chemical Industry Co., Ltd.（Dongming Jujin Chemical Industry Co., Ltd. ）

Contact:+86-533-2975022

Address:No.99 Shanquan Road, Zhangdian District
Zhengzhou Minzhong Pharmaceutical Co.,ltd

Contact:0086-371-65797115

Address:15/F,Jiangshan Bldg, NO.126 Huanghe Road,Zhengzhou, China
Hunan Haili Chemical Industry Co.,Ltd.

Contact:+86-731-85521860

Address:No.251, 2nd Section, Furong Road, Changsha,Hunan,China

Relevant to this article

Synthesis of bridged steroids. I. Steroids having a bridged bicyclo[3.2.1]octane ring system of the phyllocladene type.

Doi:10.1248/cpb.16.867
(1968)
Doi:10.1007/BF00564122
()
Biphenylsulfonamide endothelin receptor antagonists. 4. Discovery of N-[[2′-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4- (2-oxazolyl)[1,1′-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide (BMS-207940), a highly potent and orally active ET_A s

Doi:10.1021/jm020289q
(2003)
The dipolar aprotic-protic solution effects in the nucleophilic substitution of the cholesteryl tosylates

Doi:10.1002/jlac.19687140116
(1968)
Doi:10.1016/S0040-4039(00)89672-0
(1968)
Preparation of sterically constrained arylalkyne oligomers

Doi:10.1016/S0040-4020(97)00762-X
(1997)

Article Doi